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You searched for subject:(Metallo catalyzed cross coupling). Showing records 1 – 30 of 13765 total matches.

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1. Prieur, Vanessa. Pyrrolo[2,3-d]pyrimidines : conception, synthèse, fonctionnalisation : Pyrrolo[2,3-d]pyrimidines : design, synthesis, functionalisation.

Degree: Docteur es, Chimie organique, 2015, Université d'Orléans

Les pyrrolo[2,3-d]pyrimidines, également connues sous le nom de 7-déazapurines, sont une classe importante d’hétérocycliques aromatiques, de par leurs potentiels biologiques (antitumoral, antiinflammatoire, antibactérien, etc.). C’est… (more)

Subjects/Keywords: Pyrrolo[2,3-d]pyrimidines; Couplage métallo-catalysé; Suzuki-Miyaura; Liebeskind-Srogl; Amination; Irradiation micro-ondes; Pyrrolo[2,3-d]pyrimidines; Metallo-catalyzed cross coupling; Suzuki-Miyaura; Liebeskind-Srogl; Amination; Micro-waves irradiations; 547.59

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APA (6th Edition):

Prieur, V. (2015). Pyrrolo[2,3-d]pyrimidines : conception, synthèse, fonctionnalisation : Pyrrolo[2,3-d]pyrimidines : design, synthesis, functionalisation. (Doctoral Dissertation). Université d'Orléans. Retrieved from http://www.theses.fr/2015ORLE2072

Chicago Manual of Style (16th Edition):

Prieur, Vanessa. “Pyrrolo[2,3-d]pyrimidines : conception, synthèse, fonctionnalisation : Pyrrolo[2,3-d]pyrimidines : design, synthesis, functionalisation.” 2015. Doctoral Dissertation, Université d'Orléans. Accessed January 26, 2021. http://www.theses.fr/2015ORLE2072.

MLA Handbook (7th Edition):

Prieur, Vanessa. “Pyrrolo[2,3-d]pyrimidines : conception, synthèse, fonctionnalisation : Pyrrolo[2,3-d]pyrimidines : design, synthesis, functionalisation.” 2015. Web. 26 Jan 2021.

Vancouver:

Prieur V. Pyrrolo[2,3-d]pyrimidines : conception, synthèse, fonctionnalisation : Pyrrolo[2,3-d]pyrimidines : design, synthesis, functionalisation. [Internet] [Doctoral dissertation]. Université d'Orléans; 2015. [cited 2021 Jan 26]. Available from: http://www.theses.fr/2015ORLE2072.

Council of Science Editors:

Prieur V. Pyrrolo[2,3-d]pyrimidines : conception, synthèse, fonctionnalisation : Pyrrolo[2,3-d]pyrimidines : design, synthesis, functionalisation. [Doctoral Dissertation]. Université d'Orléans; 2015. Available from: http://www.theses.fr/2015ORLE2072

2. Marie, Emilie. Synthèse d'imidazo (1,2-a) pyridines à activité antivirale à l'encontre des virus de l'hépatite C et de la diarrhée virale bovine : Synthesis of imidazo[1,2-a]pyridines with antiviral activity against hepatisis C and bovine viral diarrhea viruses.

Degree: Docteur es, Sciences de la vie et de la santé, spécialité Chimie thérapeutique, 2012, Université François-Rabelais de Tours

L’hépatite C est une maladie silencieuse, souvent asymptomatique, mais qui entraîne des lésions du foie et peut évoluer vers une cirrhose et, dans certains cas,… (more)

Subjects/Keywords: Hépatite C; VHC; VDVB; Imidazo[1,2-a]pyridine; Pharmacomodulation; Bifonctionnalisation; Couplages métallo-catalysés; Évaluation biologique; Hepatitis C; HCV; BVDV; Imidazo [1,2-a]pyridine; Pharmacomodulation; Bifunctionalization; Metallo-catalyzed cross-coupling; Biological evaluation

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APA (6th Edition):

Marie, E. (2012). Synthèse d'imidazo (1,2-a) pyridines à activité antivirale à l'encontre des virus de l'hépatite C et de la diarrhée virale bovine : Synthesis of imidazo[1,2-a]pyridines with antiviral activity against hepatisis C and bovine viral diarrhea viruses. (Doctoral Dissertation). Université François-Rabelais de Tours. Retrieved from http://www.theses.fr/2012TOUR3802

Chicago Manual of Style (16th Edition):

Marie, Emilie. “Synthèse d'imidazo (1,2-a) pyridines à activité antivirale à l'encontre des virus de l'hépatite C et de la diarrhée virale bovine : Synthesis of imidazo[1,2-a]pyridines with antiviral activity against hepatisis C and bovine viral diarrhea viruses.” 2012. Doctoral Dissertation, Université François-Rabelais de Tours. Accessed January 26, 2021. http://www.theses.fr/2012TOUR3802.

MLA Handbook (7th Edition):

Marie, Emilie. “Synthèse d'imidazo (1,2-a) pyridines à activité antivirale à l'encontre des virus de l'hépatite C et de la diarrhée virale bovine : Synthesis of imidazo[1,2-a]pyridines with antiviral activity against hepatisis C and bovine viral diarrhea viruses.” 2012. Web. 26 Jan 2021.

Vancouver:

Marie E. Synthèse d'imidazo (1,2-a) pyridines à activité antivirale à l'encontre des virus de l'hépatite C et de la diarrhée virale bovine : Synthesis of imidazo[1,2-a]pyridines with antiviral activity against hepatisis C and bovine viral diarrhea viruses. [Internet] [Doctoral dissertation]. Université François-Rabelais de Tours; 2012. [cited 2021 Jan 26]. Available from: http://www.theses.fr/2012TOUR3802.

Council of Science Editors:

Marie E. Synthèse d'imidazo (1,2-a) pyridines à activité antivirale à l'encontre des virus de l'hépatite C et de la diarrhée virale bovine : Synthesis of imidazo[1,2-a]pyridines with antiviral activity against hepatisis C and bovine viral diarrhea viruses. [Doctoral Dissertation]. Université François-Rabelais de Tours; 2012. Available from: http://www.theses.fr/2012TOUR3802


University of Rochester

3. Anka-Lufford, Lukiana L. (1988 - ). Nickel-catalyzed reductive coupling of aryl halides with alkyl electrophiles.

Degree: PhD, 2016, University of Rochester

 The direct transition-metal catalyzed cross-coupling of two different electrophiles is a fast emerging synthetic method, as it avoids the use of carbon nucleophiles. Despite being… (more)

Subjects/Keywords: Alkyl electrophiles; Aryl halides; Cross-coupling; Nickel-catalyzed

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APA (6th Edition):

Anka-Lufford, L. L. (. -. ). (2016). Nickel-catalyzed reductive coupling of aryl halides with alkyl electrophiles. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/30406

Chicago Manual of Style (16th Edition):

Anka-Lufford, Lukiana L (1988 - ). “Nickel-catalyzed reductive coupling of aryl halides with alkyl electrophiles.” 2016. Doctoral Dissertation, University of Rochester. Accessed January 26, 2021. http://hdl.handle.net/1802/30406.

MLA Handbook (7th Edition):

Anka-Lufford, Lukiana L (1988 - ). “Nickel-catalyzed reductive coupling of aryl halides with alkyl electrophiles.” 2016. Web. 26 Jan 2021.

Vancouver:

Anka-Lufford LL(-). Nickel-catalyzed reductive coupling of aryl halides with alkyl electrophiles. [Internet] [Doctoral dissertation]. University of Rochester; 2016. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/1802/30406.

Council of Science Editors:

Anka-Lufford LL(-). Nickel-catalyzed reductive coupling of aryl halides with alkyl electrophiles. [Doctoral Dissertation]. University of Rochester; 2016. Available from: http://hdl.handle.net/1802/30406


University of Illinois – Urbana-Champaign

4. Bailey, Aaron D. Palladium catalyzed cross-coupling reactions of allyl- and vinylsilanes.

Degree: MS, 0335, 2011, University of Illinois – Urbana-Champaign

 Palladium-catalyzed cross-coupling of ??-substituted allylic silanolates with aryl bromides was investigated. It was discovered that ??-selectivity is heavily influenced by the substituents at silicon. It… (more)

Subjects/Keywords: Palladium-catalyzed cross-coupling reactions; allylic silanes; vinylsilanes

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APA (6th Edition):

Bailey, A. D. (2011). Palladium catalyzed cross-coupling reactions of allyl- and vinylsilanes. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/24450

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Bailey, Aaron D. “Palladium catalyzed cross-coupling reactions of allyl- and vinylsilanes.” 2011. Thesis, University of Illinois – Urbana-Champaign. Accessed January 26, 2021. http://hdl.handle.net/2142/24450.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Bailey, Aaron D. “Palladium catalyzed cross-coupling reactions of allyl- and vinylsilanes.” 2011. Web. 26 Jan 2021.

Vancouver:

Bailey AD. Palladium catalyzed cross-coupling reactions of allyl- and vinylsilanes. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2011. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/2142/24450.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Bailey AD. Palladium catalyzed cross-coupling reactions of allyl- and vinylsilanes. [Thesis]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/24450

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Université de Lorraine

5. Jasselin-Hinschberger, Adeline. Polyfonctionnalisations sélectives par voie organométallique en série furopyridines : développement de procédés séquentiels et "one-pot" originaux : Selective polyfunctionalization of furopyridines through organometallic synthetic pathways : development of efficient sequential and one-pot processes.

Degree: Docteur es, Chimie, 2014, Université de Lorraine

Le travail décrit dans ce mémoire concerne l'étude de la métallation régiosélective d’un bicycle fusionné: la furo[3,2-B]pyridine. L'influence de la nature du système basique sur… (more)

Subjects/Keywords: Chimie organométallique polaire; Couplages métallo-Catalysés; Séquences « one-Pot »; Furo[3,2-B]pyridine; Hétérocycles aza-π-Déficients; Réactions de métallation; Superbase [n-BuLi/LiDMAE]; Polar organometallic chemistry; Metallo-Catalyzed cross coupling; « One-Pot » processes; Furo[3,2-B]pyridine; Aza-π-Deficient heterocycles; Metalation reactions; [n-BuLi/LiDMAE] superbase; 547.05

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APA (6th Edition):

Jasselin-Hinschberger, A. (2014). Polyfonctionnalisations sélectives par voie organométallique en série furopyridines : développement de procédés séquentiels et "one-pot" originaux : Selective polyfunctionalization of furopyridines through organometallic synthetic pathways : development of efficient sequential and one-pot processes. (Doctoral Dissertation). Université de Lorraine. Retrieved from http://www.theses.fr/2014LORR0163

Chicago Manual of Style (16th Edition):

Jasselin-Hinschberger, Adeline. “Polyfonctionnalisations sélectives par voie organométallique en série furopyridines : développement de procédés séquentiels et "one-pot" originaux : Selective polyfunctionalization of furopyridines through organometallic synthetic pathways : development of efficient sequential and one-pot processes.” 2014. Doctoral Dissertation, Université de Lorraine. Accessed January 26, 2021. http://www.theses.fr/2014LORR0163.

MLA Handbook (7th Edition):

Jasselin-Hinschberger, Adeline. “Polyfonctionnalisations sélectives par voie organométallique en série furopyridines : développement de procédés séquentiels et "one-pot" originaux : Selective polyfunctionalization of furopyridines through organometallic synthetic pathways : development of efficient sequential and one-pot processes.” 2014. Web. 26 Jan 2021.

Vancouver:

Jasselin-Hinschberger A. Polyfonctionnalisations sélectives par voie organométallique en série furopyridines : développement de procédés séquentiels et "one-pot" originaux : Selective polyfunctionalization of furopyridines through organometallic synthetic pathways : development of efficient sequential and one-pot processes. [Internet] [Doctoral dissertation]. Université de Lorraine; 2014. [cited 2021 Jan 26]. Available from: http://www.theses.fr/2014LORR0163.

Council of Science Editors:

Jasselin-Hinschberger A. Polyfonctionnalisations sélectives par voie organométallique en série furopyridines : développement de procédés séquentiels et "one-pot" originaux : Selective polyfunctionalization of furopyridines through organometallic synthetic pathways : development of efficient sequential and one-pot processes. [Doctoral Dissertation]. Université de Lorraine; 2014. Available from: http://www.theses.fr/2014LORR0163


University of Alberta

6. Lee, Jack C. H. Preparation and Synthetic Applications of Chiral Alkyl Boronates and Unsaturated Alkenyl Boronates.

Degree: PhD, Department of Chemistry, 2013, University of Alberta

 As Organic Chemistry evolves into the 21st Century, the goal of this discipline has altered dramatically from merely accessing target molecules to efficiently synthesizing these… (more)

Subjects/Keywords: Gold-catalyzed cycloisomerization; Suzuki-Miyaura cross-coupling; Chiral alkyl boronates; Heck reaction; Enantioselective conjugate addition

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APA (6th Edition):

Lee, J. C. H. (2013). Preparation and Synthetic Applications of Chiral Alkyl Boronates and Unsaturated Alkenyl Boronates. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/qn59q550n

Chicago Manual of Style (16th Edition):

Lee, Jack C H. “Preparation and Synthetic Applications of Chiral Alkyl Boronates and Unsaturated Alkenyl Boronates.” 2013. Doctoral Dissertation, University of Alberta. Accessed January 26, 2021. https://era.library.ualberta.ca/files/qn59q550n.

MLA Handbook (7th Edition):

Lee, Jack C H. “Preparation and Synthetic Applications of Chiral Alkyl Boronates and Unsaturated Alkenyl Boronates.” 2013. Web. 26 Jan 2021.

Vancouver:

Lee JCH. Preparation and Synthetic Applications of Chiral Alkyl Boronates and Unsaturated Alkenyl Boronates. [Internet] [Doctoral dissertation]. University of Alberta; 2013. [cited 2021 Jan 26]. Available from: https://era.library.ualberta.ca/files/qn59q550n.

Council of Science Editors:

Lee JCH. Preparation and Synthetic Applications of Chiral Alkyl Boronates and Unsaturated Alkenyl Boronates. [Doctoral Dissertation]. University of Alberta; 2013. Available from: https://era.library.ualberta.ca/files/qn59q550n

7. Naohisa, Nakagawa. Selective Synthesis of Alkynes and Alkenes Using Iron-Catalyzed Cross-Coupling and Organometallic Addition Reactions : 鉄触媒クロスカップリングと有機金属付加反応を用いるアルキン・アルケン類の選択的合成.

Degree: 博士(工学), 2015, Kyoto University / 京都大学

新制・課程博士

甲第19181号

工博第4058号

Subjects/Keywords: iron-catalyzed; cross-coupling; alkyne; alkene

Page 1 Page 2 Page 3 Page 4

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APA (6th Edition):

Naohisa, N. (2015). Selective Synthesis of Alkynes and Alkenes Using Iron-Catalyzed Cross-Coupling and Organometallic Addition Reactions : 鉄触媒クロスカップリングと有機金属付加反応を用いるアルキン・アルケン類の選択的合成. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/200444 ; http://dx.doi.org/10.14989/doctor.k19181

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Naohisa, Nakagawa. “Selective Synthesis of Alkynes and Alkenes Using Iron-Catalyzed Cross-Coupling and Organometallic Addition Reactions : 鉄触媒クロスカップリングと有機金属付加反応を用いるアルキン・アルケン類の選択的合成.” 2015. Thesis, Kyoto University / 京都大学. Accessed January 26, 2021. http://hdl.handle.net/2433/200444 ; http://dx.doi.org/10.14989/doctor.k19181.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Naohisa, Nakagawa. “Selective Synthesis of Alkynes and Alkenes Using Iron-Catalyzed Cross-Coupling and Organometallic Addition Reactions : 鉄触媒クロスカップリングと有機金属付加反応を用いるアルキン・アルケン類の選択的合成.” 2015. Web. 26 Jan 2021.

Vancouver:

Naohisa N. Selective Synthesis of Alkynes and Alkenes Using Iron-Catalyzed Cross-Coupling and Organometallic Addition Reactions : 鉄触媒クロスカップリングと有機金属付加反応を用いるアルキン・アルケン類の選択的合成. [Internet] [Thesis]. Kyoto University / 京都大学; 2015. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/2433/200444 ; http://dx.doi.org/10.14989/doctor.k19181.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Naohisa N. Selective Synthesis of Alkynes and Alkenes Using Iron-Catalyzed Cross-Coupling and Organometallic Addition Reactions : 鉄触媒クロスカップリングと有機金属付加反応を用いるアルキン・アルケン類の選択的合成. [Thesis]. Kyoto University / 京都大学; 2015. Available from: http://hdl.handle.net/2433/200444 ; http://dx.doi.org/10.14989/doctor.k19181

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Boston College

8. Mako, Teresa Louise. Electronic, Structural, and Catalytic Analyses of Iron Pincer Complexes and Methods for the Direct Functionalization of Lactide.

Degree: MS, Chemistry, 2017, Boston College

 Chapter 1: A review of recent iron catalyzed cross coupling advances. Abstract: Herein, advances in iron catalyzed cross coupling from 2010-2015 are thoroughly reviewed. Newly… (more)

Subjects/Keywords: iron carbene catalyst; Iron catalyzed cross coupling; Iron pincer complex; lactide functionalizaton; soft enolization

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APA (6th Edition):

Mako, T. L. (2017). Electronic, Structural, and Catalytic Analyses of Iron Pincer Complexes and Methods for the Direct Functionalization of Lactide. (Masters Thesis). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:107588

Chicago Manual of Style (16th Edition):

Mako, Teresa Louise. “Electronic, Structural, and Catalytic Analyses of Iron Pincer Complexes and Methods for the Direct Functionalization of Lactide.” 2017. Masters Thesis, Boston College. Accessed January 26, 2021. http://dlib.bc.edu/islandora/object/bc-ir:107588.

MLA Handbook (7th Edition):

Mako, Teresa Louise. “Electronic, Structural, and Catalytic Analyses of Iron Pincer Complexes and Methods for the Direct Functionalization of Lactide.” 2017. Web. 26 Jan 2021.

Vancouver:

Mako TL. Electronic, Structural, and Catalytic Analyses of Iron Pincer Complexes and Methods for the Direct Functionalization of Lactide. [Internet] [Masters thesis]. Boston College; 2017. [cited 2021 Jan 26]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:107588.

Council of Science Editors:

Mako TL. Electronic, Structural, and Catalytic Analyses of Iron Pincer Complexes and Methods for the Direct Functionalization of Lactide. [Masters Thesis]. Boston College; 2017. Available from: http://dlib.bc.edu/islandora/object/bc-ir:107588


University of Washington

9. Lesniak, Valerie Ann. Palladium-Catalyzed Cross-Couplings of 2-Alkylaziridines and Alkenylboronic Acids.

Degree: 2016, University of Washington

 A new method to synthesize substituted homoallylic amines is reported. Homoallylic amines are important structural moieties in natural products and pharmaceutical agents. The reaction couples… (more)

Subjects/Keywords: alkenylboronic acid; aziridine; boronic acid; cross-coupling; homoallylic amine; Palladium-catalyzed; Chemistry; Organic chemistry; chemistry

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APA (6th Edition):

Lesniak, V. A. (2016). Palladium-Catalyzed Cross-Couplings of 2-Alkylaziridines and Alkenylboronic Acids. (Thesis). University of Washington. Retrieved from http://hdl.handle.net/1773/37060

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Lesniak, Valerie Ann. “Palladium-Catalyzed Cross-Couplings of 2-Alkylaziridines and Alkenylboronic Acids.” 2016. Thesis, University of Washington. Accessed January 26, 2021. http://hdl.handle.net/1773/37060.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Lesniak, Valerie Ann. “Palladium-Catalyzed Cross-Couplings of 2-Alkylaziridines and Alkenylboronic Acids.” 2016. Web. 26 Jan 2021.

Vancouver:

Lesniak VA. Palladium-Catalyzed Cross-Couplings of 2-Alkylaziridines and Alkenylboronic Acids. [Internet] [Thesis]. University of Washington; 2016. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/1773/37060.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Lesniak VA. Palladium-Catalyzed Cross-Couplings of 2-Alkylaziridines and Alkenylboronic Acids. [Thesis]. University of Washington; 2016. Available from: http://hdl.handle.net/1773/37060

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Pennsylvania

10. McGrew, Genette I. Activation and Catalytic Bond Forming Reactions at Carbon-Hydrogen Bonds of η6-Tricarbonylchromium-Coordinated Benzylic Arenes.

Degree: 2011, University of Pennsylvania

 Polyarylmethanes are an extremely valuable molecular scaffold used in fields ranging from materials chemistry to medicinal chemistry. They are found in dyes and semiconductor dopants… (more)

Subjects/Keywords: tricarbonylchromium; palladium-catalyzed; cross-coupling; asymmetric; organolithium; polyarylmethanes; Inorganic Chemistry; Organic Chemistry

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APA (6th Edition):

McGrew, G. I. (2011). Activation and Catalytic Bond Forming Reactions at Carbon-Hydrogen Bonds of η6-Tricarbonylchromium-Coordinated Benzylic Arenes. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/964

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

McGrew, Genette I. “Activation and Catalytic Bond Forming Reactions at Carbon-Hydrogen Bonds of η6-Tricarbonylchromium-Coordinated Benzylic Arenes.” 2011. Thesis, University of Pennsylvania. Accessed January 26, 2021. https://repository.upenn.edu/edissertations/964.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

McGrew, Genette I. “Activation and Catalytic Bond Forming Reactions at Carbon-Hydrogen Bonds of η6-Tricarbonylchromium-Coordinated Benzylic Arenes.” 2011. Web. 26 Jan 2021.

Vancouver:

McGrew GI. Activation and Catalytic Bond Forming Reactions at Carbon-Hydrogen Bonds of η6-Tricarbonylchromium-Coordinated Benzylic Arenes. [Internet] [Thesis]. University of Pennsylvania; 2011. [cited 2021 Jan 26]. Available from: https://repository.upenn.edu/edissertations/964.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

McGrew GI. Activation and Catalytic Bond Forming Reactions at Carbon-Hydrogen Bonds of η6-Tricarbonylchromium-Coordinated Benzylic Arenes. [Thesis]. University of Pennsylvania; 2011. Available from: https://repository.upenn.edu/edissertations/964

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Kyoto University

11. Naohisa, Nakagawa. Selective Synthesis of Alkynes and Alkenes Using Iron-Catalyzed Cross-Coupling and Organometallic Addition Reactions .

Degree: 2015, Kyoto University

Subjects/Keywords: iron-catalyzed; cross-coupling; alkyne; alkene

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APA (6th Edition):

Naohisa, N. (2015). Selective Synthesis of Alkynes and Alkenes Using Iron-Catalyzed Cross-Coupling and Organometallic Addition Reactions . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/200444

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Naohisa, Nakagawa. “Selective Synthesis of Alkynes and Alkenes Using Iron-Catalyzed Cross-Coupling and Organometallic Addition Reactions .” 2015. Thesis, Kyoto University. Accessed January 26, 2021. http://hdl.handle.net/2433/200444.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Naohisa, Nakagawa. “Selective Synthesis of Alkynes and Alkenes Using Iron-Catalyzed Cross-Coupling and Organometallic Addition Reactions .” 2015. Web. 26 Jan 2021.

Vancouver:

Naohisa N. Selective Synthesis of Alkynes and Alkenes Using Iron-Catalyzed Cross-Coupling and Organometallic Addition Reactions . [Internet] [Thesis]. Kyoto University; 2015. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/2433/200444.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Naohisa N. Selective Synthesis of Alkynes and Alkenes Using Iron-Catalyzed Cross-Coupling and Organometallic Addition Reactions . [Thesis]. Kyoto University; 2015. Available from: http://hdl.handle.net/2433/200444

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Illinois – Chicago

12. Mamidipalli, Phani Raja P. Mechanism of Copper Catalyzed Diazo Coupling and its Applications & Reactions of Multiynes.

Degree: 2015, University of Illinois – Chicago

 This thesis has two main parts. Part I is composed of two chapters which describes mechanistic investigation of copper catalyzed reactions of diazo compounds followed… (more)

Subjects/Keywords: Copper catalyzed coupling; HDDA reaction

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APA (6th Edition):

Mamidipalli, P. R. P. (2015). Mechanism of Copper Catalyzed Diazo Coupling and its Applications & Reactions of Multiynes. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/19456

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Mamidipalli, Phani Raja P. “Mechanism of Copper Catalyzed Diazo Coupling and its Applications & Reactions of Multiynes.” 2015. Thesis, University of Illinois – Chicago. Accessed January 26, 2021. http://hdl.handle.net/10027/19456.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Mamidipalli, Phani Raja P. “Mechanism of Copper Catalyzed Diazo Coupling and its Applications & Reactions of Multiynes.” 2015. Web. 26 Jan 2021.

Vancouver:

Mamidipalli PRP. Mechanism of Copper Catalyzed Diazo Coupling and its Applications & Reactions of Multiynes. [Internet] [Thesis]. University of Illinois – Chicago; 2015. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/10027/19456.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Mamidipalli PRP. Mechanism of Copper Catalyzed Diazo Coupling and its Applications & Reactions of Multiynes. [Thesis]. University of Illinois – Chicago; 2015. Available from: http://hdl.handle.net/10027/19456

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


McMaster University

13. Todorovic, Nikola. DEVELOPMENT AND APPLICATION OF SYNTHETIC PROTOCOLS FOR THE GENERATION OF HETEROCYCLIC COMPOUND LIBRARIES.

Degree: PhD, 2012, McMaster University

The development of parallel syntheses that allow for rapid access to compound libraries is widely sought after in drug development and in the study… (more)

Subjects/Keywords: Compound libraries; Isoquinolines; Pyrazolopyrimidines; Toxoflavin; Palladium-catalyzed cross-coupling; Microwave-assisted heating; Organic Chemistry; Organic Chemistry

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APA (6th Edition):

Todorovic, N. (2012). DEVELOPMENT AND APPLICATION OF SYNTHETIC PROTOCOLS FOR THE GENERATION OF HETEROCYCLIC COMPOUND LIBRARIES. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/12471

Chicago Manual of Style (16th Edition):

Todorovic, Nikola. “DEVELOPMENT AND APPLICATION OF SYNTHETIC PROTOCOLS FOR THE GENERATION OF HETEROCYCLIC COMPOUND LIBRARIES.” 2012. Doctoral Dissertation, McMaster University. Accessed January 26, 2021. http://hdl.handle.net/11375/12471.

MLA Handbook (7th Edition):

Todorovic, Nikola. “DEVELOPMENT AND APPLICATION OF SYNTHETIC PROTOCOLS FOR THE GENERATION OF HETEROCYCLIC COMPOUND LIBRARIES.” 2012. Web. 26 Jan 2021.

Vancouver:

Todorovic N. DEVELOPMENT AND APPLICATION OF SYNTHETIC PROTOCOLS FOR THE GENERATION OF HETEROCYCLIC COMPOUND LIBRARIES. [Internet] [Doctoral dissertation]. McMaster University; 2012. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/11375/12471.

Council of Science Editors:

Todorovic N. DEVELOPMENT AND APPLICATION OF SYNTHETIC PROTOCOLS FOR THE GENERATION OF HETEROCYCLIC COMPOUND LIBRARIES. [Doctoral Dissertation]. McMaster University; 2012. Available from: http://hdl.handle.net/11375/12471

14. Neilde, Kevin. Pharmacomodulation anti-infectieuse en série 5-nitroimidazole : couplages pallado-catalysés et réactions par transfert monoélectronique. : Anti-infectious pharmacomodulation in 5-nitroimidazole serie : pallado-catalyzed cross-coupling and single electron transfer reactions.

Degree: Docteur es, Sciences Chimiques, 2014, Aix Marseille Université

Ce travail s’inscrit dans la recherche de nouveaux 5-nitroimidazoles fonctionnalisés à visée thérapeutique. L’étude de la réactivité du 4-bromo-1,2-diméthyl-5-nitro-1H-imidazole vis-à-vis des réactions de couplages de… (more)

Subjects/Keywords: 5-Nitroimidazole; Couplages pallado-Catalysés; Transfert monoélectronique; Srn1; Tdae.; 5-Nitroimidazole; Pallado-Catalyzed cross-Coupling; Single electron transfer; Srn1; Tdae.

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APA (6th Edition):

Neilde, K. (2014). Pharmacomodulation anti-infectieuse en série 5-nitroimidazole : couplages pallado-catalysés et réactions par transfert monoélectronique. : Anti-infectious pharmacomodulation in 5-nitroimidazole serie : pallado-catalyzed cross-coupling and single electron transfer reactions. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2014AIXM5502

Chicago Manual of Style (16th Edition):

Neilde, Kevin. “Pharmacomodulation anti-infectieuse en série 5-nitroimidazole : couplages pallado-catalysés et réactions par transfert monoélectronique. : Anti-infectious pharmacomodulation in 5-nitroimidazole serie : pallado-catalyzed cross-coupling and single electron transfer reactions.” 2014. Doctoral Dissertation, Aix Marseille Université. Accessed January 26, 2021. http://www.theses.fr/2014AIXM5502.

MLA Handbook (7th Edition):

Neilde, Kevin. “Pharmacomodulation anti-infectieuse en série 5-nitroimidazole : couplages pallado-catalysés et réactions par transfert monoélectronique. : Anti-infectious pharmacomodulation in 5-nitroimidazole serie : pallado-catalyzed cross-coupling and single electron transfer reactions.” 2014. Web. 26 Jan 2021.

Vancouver:

Neilde K. Pharmacomodulation anti-infectieuse en série 5-nitroimidazole : couplages pallado-catalysés et réactions par transfert monoélectronique. : Anti-infectious pharmacomodulation in 5-nitroimidazole serie : pallado-catalyzed cross-coupling and single electron transfer reactions. [Internet] [Doctoral dissertation]. Aix Marseille Université 2014. [cited 2021 Jan 26]. Available from: http://www.theses.fr/2014AIXM5502.

Council of Science Editors:

Neilde K. Pharmacomodulation anti-infectieuse en série 5-nitroimidazole : couplages pallado-catalysés et réactions par transfert monoélectronique. : Anti-infectious pharmacomodulation in 5-nitroimidazole serie : pallado-catalyzed cross-coupling and single electron transfer reactions. [Doctoral Dissertation]. Aix Marseille Université 2014. Available from: http://www.theses.fr/2014AIXM5502


Florida International University

15. Pitteloud, Jean-Philippe. New Organogermanium Substrates for Palladium-Catalyzed Cross-Coupling Reactions. Application of Organogermanes towards the Synthesis of Carbon-5 Modified Uridine Analogues.

Degree: Chemistry, 2010, Florida International University

  The diverse biological properties exhibited by uridine analogues modified at carbon-5 of the uracil base have attracted special interest to the development of efficient… (more)

Subjects/Keywords: ORGANOGERMANES; PALLADIUM-CATALYZED; CROSS-COUPLING; TRANSMETALLATION; URIDINE; NUCLEOSIDES

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APA (6th Edition):

Pitteloud, J. (2010). New Organogermanium Substrates for Palladium-Catalyzed Cross-Coupling Reactions. Application of Organogermanes towards the Synthesis of Carbon-5 Modified Uridine Analogues. (Thesis). Florida International University. Retrieved from https://digitalcommons.fiu.edu/etd/170 ; 10.25148/etd.FI10041621 ; FI10041621

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Pitteloud, Jean-Philippe. “New Organogermanium Substrates for Palladium-Catalyzed Cross-Coupling Reactions. Application of Organogermanes towards the Synthesis of Carbon-5 Modified Uridine Analogues.” 2010. Thesis, Florida International University. Accessed January 26, 2021. https://digitalcommons.fiu.edu/etd/170 ; 10.25148/etd.FI10041621 ; FI10041621.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Pitteloud, Jean-Philippe. “New Organogermanium Substrates for Palladium-Catalyzed Cross-Coupling Reactions. Application of Organogermanes towards the Synthesis of Carbon-5 Modified Uridine Analogues.” 2010. Web. 26 Jan 2021.

Vancouver:

Pitteloud J. New Organogermanium Substrates for Palladium-Catalyzed Cross-Coupling Reactions. Application of Organogermanes towards the Synthesis of Carbon-5 Modified Uridine Analogues. [Internet] [Thesis]. Florida International University; 2010. [cited 2021 Jan 26]. Available from: https://digitalcommons.fiu.edu/etd/170 ; 10.25148/etd.FI10041621 ; FI10041621.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Pitteloud J. New Organogermanium Substrates for Palladium-Catalyzed Cross-Coupling Reactions. Application of Organogermanes towards the Synthesis of Carbon-5 Modified Uridine Analogues. [Thesis]. Florida International University; 2010. Available from: https://digitalcommons.fiu.edu/etd/170 ; 10.25148/etd.FI10041621 ; FI10041621

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Florida International University

16. Liang, Yong. Novel Approaches for the Synthesis of C-5 Modified Pyrimidine Nucleosides.

Degree: PhD, Chemistry, 2014, Florida International University

  The antiviral or anticancer activities of C-5 modified pyrimidine nucleoside analogues validate the need for the development of their syntheses. In the first half… (more)

Subjects/Keywords: Nucleoside; Pd-catalyzed Cross-coupling; Palladium; Click Chemistry; Hydrogermylation; C-H activation; Direct Arylation; Organic Chemistry

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APA (6th Edition):

Liang, Y. (2014). Novel Approaches for the Synthesis of C-5 Modified Pyrimidine Nucleosides. (Doctoral Dissertation). Florida International University. Retrieved from https://digitalcommons.fiu.edu/etd/1591 ; 10.25148/etd.FI14110716 ; FI14110716

Chicago Manual of Style (16th Edition):

Liang, Yong. “Novel Approaches for the Synthesis of C-5 Modified Pyrimidine Nucleosides.” 2014. Doctoral Dissertation, Florida International University. Accessed January 26, 2021. https://digitalcommons.fiu.edu/etd/1591 ; 10.25148/etd.FI14110716 ; FI14110716.

MLA Handbook (7th Edition):

Liang, Yong. “Novel Approaches for the Synthesis of C-5 Modified Pyrimidine Nucleosides.” 2014. Web. 26 Jan 2021.

Vancouver:

Liang Y. Novel Approaches for the Synthesis of C-5 Modified Pyrimidine Nucleosides. [Internet] [Doctoral dissertation]. Florida International University; 2014. [cited 2021 Jan 26]. Available from: https://digitalcommons.fiu.edu/etd/1591 ; 10.25148/etd.FI14110716 ; FI14110716.

Council of Science Editors:

Liang Y. Novel Approaches for the Synthesis of C-5 Modified Pyrimidine Nucleosides. [Doctoral Dissertation]. Florida International University; 2014. Available from: https://digitalcommons.fiu.edu/etd/1591 ; 10.25148/etd.FI14110716 ; FI14110716


East Carolina University

17. Harris, Caleb F. Synthesis and Reactions of Novel Heteroarylzirconocene Reagents.

Degree: MS, Chemistry, 2012, East Carolina University

 The cross-coupling of metallated heteroaromatic species with aryl and heteroaryl halides is a powerful and highly desirable transformation in both the synthesis of pharmaceutical compounds… (more)

Subjects/Keywords: Chemistry; Cross-coupling; Heteroaromatic; Organometallic; Palladium-catalyzed; Zirconocene; Zirconium; Chemical tests and reagents; Organic compounds – Synthesis; Halides

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APA (6th Edition):

Harris, C. F. (2012). Synthesis and Reactions of Novel Heteroarylzirconocene Reagents. (Masters Thesis). East Carolina University. Retrieved from http://hdl.handle.net/10342/4004

Chicago Manual of Style (16th Edition):

Harris, Caleb F. “Synthesis and Reactions of Novel Heteroarylzirconocene Reagents.” 2012. Masters Thesis, East Carolina University. Accessed January 26, 2021. http://hdl.handle.net/10342/4004.

MLA Handbook (7th Edition):

Harris, Caleb F. “Synthesis and Reactions of Novel Heteroarylzirconocene Reagents.” 2012. Web. 26 Jan 2021.

Vancouver:

Harris CF. Synthesis and Reactions of Novel Heteroarylzirconocene Reagents. [Internet] [Masters thesis]. East Carolina University; 2012. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/10342/4004.

Council of Science Editors:

Harris CF. Synthesis and Reactions of Novel Heteroarylzirconocene Reagents. [Masters Thesis]. East Carolina University; 2012. Available from: http://hdl.handle.net/10342/4004


Université Paris-Sud – Paris XI

18. Roche, Maxime. Couplages pallado-catalysés de N-tosylhydrazones : synthèse d’oléfines apparentées à l’isocombrétastatine A4 : Palladium catalyzed coupling of N-tosylhydrazones : synthesis of olefines related to isocombretastatin A4.

Degree: Docteur es, Chimie thérapeutique, 2014, Université Paris-Sud – Paris XI

Les travaux rapportés dans ce mémoire concernent le développement de nouveaux couplages pallado-catalysés de N-tosylhydrazones ainsi que leurs applications à la synthèse d’analogues de l’isocombrétastatine… (more)

Subjects/Keywords: Combrétastatine; Antivasculaire; N-tosylhydrazone; Couplage pallado-catalysé; Réaction tandem; Couplage oxydatif; Combretastatin; Antivascular; N-tosylhydrazone; Palladium catalyzed cross-coupling; Tandem reaction; Oxidative coupling

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APA (6th Edition):

Roche, M. (2014). Couplages pallado-catalysés de N-tosylhydrazones : synthèse d’oléfines apparentées à l’isocombrétastatine A4 : Palladium catalyzed coupling of N-tosylhydrazones : synthesis of olefines related to isocombretastatin A4. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2014PA114843

Chicago Manual of Style (16th Edition):

Roche, Maxime. “Couplages pallado-catalysés de N-tosylhydrazones : synthèse d’oléfines apparentées à l’isocombrétastatine A4 : Palladium catalyzed coupling of N-tosylhydrazones : synthesis of olefines related to isocombretastatin A4.” 2014. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed January 26, 2021. http://www.theses.fr/2014PA114843.

MLA Handbook (7th Edition):

Roche, Maxime. “Couplages pallado-catalysés de N-tosylhydrazones : synthèse d’oléfines apparentées à l’isocombrétastatine A4 : Palladium catalyzed coupling of N-tosylhydrazones : synthesis of olefines related to isocombretastatin A4.” 2014. Web. 26 Jan 2021.

Vancouver:

Roche M. Couplages pallado-catalysés de N-tosylhydrazones : synthèse d’oléfines apparentées à l’isocombrétastatine A4 : Palladium catalyzed coupling of N-tosylhydrazones : synthesis of olefines related to isocombretastatin A4. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2014. [cited 2021 Jan 26]. Available from: http://www.theses.fr/2014PA114843.

Council of Science Editors:

Roche M. Couplages pallado-catalysés de N-tosylhydrazones : synthèse d’oléfines apparentées à l’isocombrétastatine A4 : Palladium catalyzed coupling of N-tosylhydrazones : synthesis of olefines related to isocombretastatin A4. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2014. Available from: http://www.theses.fr/2014PA114843

19. De Pascale, Martina. Conception, synthèse et évaluation biologique de perturbateurs d'interactions protéine-protéine impliquées dans l'apoptose : applications aux cancers de l'ovaire chimiorésistants : Design, synthesis and biological evaluation of protein-protein interactions disruptors, involved in apoptosis : applications to chemoresistant ovarian cancers.

Degree: Docteur es, Pharmacie, 2018, Normandie

Le cancer de l’ovaire représente la quatrième cause de décès par cancer chez la femme. En France, près de 4 500 nouveaux cas par an… (more)

Subjects/Keywords: Oligopyridine; Peptidomimétiques; Smac; Réaction metallo-catalysé; Apoptosis; Foldamers; Ovary; Peptidomimetics; Metallo-catalyzed reaction; Cancer; Bcl-2; Smac; XIAP

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APA (6th Edition):

De Pascale, M. (2018). Conception, synthèse et évaluation biologique de perturbateurs d'interactions protéine-protéine impliquées dans l'apoptose : applications aux cancers de l'ovaire chimiorésistants : Design, synthesis and biological evaluation of protein-protein interactions disruptors, involved in apoptosis : applications to chemoresistant ovarian cancers. (Doctoral Dissertation). Normandie. Retrieved from http://www.theses.fr/2018NORMC414

Chicago Manual of Style (16th Edition):

De Pascale, Martina. “Conception, synthèse et évaluation biologique de perturbateurs d'interactions protéine-protéine impliquées dans l'apoptose : applications aux cancers de l'ovaire chimiorésistants : Design, synthesis and biological evaluation of protein-protein interactions disruptors, involved in apoptosis : applications to chemoresistant ovarian cancers.” 2018. Doctoral Dissertation, Normandie. Accessed January 26, 2021. http://www.theses.fr/2018NORMC414.

MLA Handbook (7th Edition):

De Pascale, Martina. “Conception, synthèse et évaluation biologique de perturbateurs d'interactions protéine-protéine impliquées dans l'apoptose : applications aux cancers de l'ovaire chimiorésistants : Design, synthesis and biological evaluation of protein-protein interactions disruptors, involved in apoptosis : applications to chemoresistant ovarian cancers.” 2018. Web. 26 Jan 2021.

Vancouver:

De Pascale M. Conception, synthèse et évaluation biologique de perturbateurs d'interactions protéine-protéine impliquées dans l'apoptose : applications aux cancers de l'ovaire chimiorésistants : Design, synthesis and biological evaluation of protein-protein interactions disruptors, involved in apoptosis : applications to chemoresistant ovarian cancers. [Internet] [Doctoral dissertation]. Normandie; 2018. [cited 2021 Jan 26]. Available from: http://www.theses.fr/2018NORMC414.

Council of Science Editors:

De Pascale M. Conception, synthèse et évaluation biologique de perturbateurs d'interactions protéine-protéine impliquées dans l'apoptose : applications aux cancers de l'ovaire chimiorésistants : Design, synthesis and biological evaluation of protein-protein interactions disruptors, involved in apoptosis : applications to chemoresistant ovarian cancers. [Doctoral Dissertation]. Normandie; 2018. Available from: http://www.theses.fr/2018NORMC414

20. Mathias, Fanny. Synthèse et évaluation biologique de nouveaux nitroimidazoles : challenges et recherche de nouvelles relations structure-activité : Synthesis and biological evaluation of new nitroimidazoles : challenges and search for new structure-activity relationships.

Degree: Docteur es, Sciences Chimiques. Chimie organique, 2017, Aix Marseille Université

Ce travail de thèse est consacré à la synthèse et l’évaluation biologique de nouveaux nitromidazoles à potentialités anti-infectieuses. Dans les trois premiers chapitres, nous avons… (more)

Subjects/Keywords: 5-Nitroimidazole; Nitroimidazooxazole; Couplages pallado-Catalysés; Transfert monoélectronique; Bactéries anaérobies; Trichomonas vaginalis; Leishmania donovani; 5-Nitroimidazole; Nitroimidazooxazole; Pallado-Catalyzed cross-Coupling; Single electron transfer; Anaerobic bacteria; Trichomonas vaginalis; Leishmania donovani

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APA (6th Edition):

Mathias, F. (2017). Synthèse et évaluation biologique de nouveaux nitroimidazoles : challenges et recherche de nouvelles relations structure-activité : Synthesis and biological evaluation of new nitroimidazoles : challenges and search for new structure-activity relationships. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2017AIXM0591

Chicago Manual of Style (16th Edition):

Mathias, Fanny. “Synthèse et évaluation biologique de nouveaux nitroimidazoles : challenges et recherche de nouvelles relations structure-activité : Synthesis and biological evaluation of new nitroimidazoles : challenges and search for new structure-activity relationships.” 2017. Doctoral Dissertation, Aix Marseille Université. Accessed January 26, 2021. http://www.theses.fr/2017AIXM0591.

MLA Handbook (7th Edition):

Mathias, Fanny. “Synthèse et évaluation biologique de nouveaux nitroimidazoles : challenges et recherche de nouvelles relations structure-activité : Synthesis and biological evaluation of new nitroimidazoles : challenges and search for new structure-activity relationships.” 2017. Web. 26 Jan 2021.

Vancouver:

Mathias F. Synthèse et évaluation biologique de nouveaux nitroimidazoles : challenges et recherche de nouvelles relations structure-activité : Synthesis and biological evaluation of new nitroimidazoles : challenges and search for new structure-activity relationships. [Internet] [Doctoral dissertation]. Aix Marseille Université 2017. [cited 2021 Jan 26]. Available from: http://www.theses.fr/2017AIXM0591.

Council of Science Editors:

Mathias F. Synthèse et évaluation biologique de nouveaux nitroimidazoles : challenges et recherche de nouvelles relations structure-activité : Synthesis and biological evaluation of new nitroimidazoles : challenges and search for new structure-activity relationships. [Doctoral Dissertation]. Aix Marseille Université 2017. Available from: http://www.theses.fr/2017AIXM0591

21. Naas, Mohammed. Synthèse et fonctionnalisation de nouveaux dérivés d’indazoles à visée thérapeutique : Synthesis of new indazoles derivatives with therapeutic potential.

Degree: Docteur es, Chimie organique. Pharmacochimie, 2016, Orléans; Université Mohamed V

L’accès à de nouveaux composés hétérocycliques originaux biologiquement actifs nécessite la mise au point de nouvelles méthodes de synthèse rapides et efficaces. Dans ce contexte,… (more)

Subjects/Keywords: Indazoles; Suzuki-Miyaura; (hétéro)arylation directe; Alcénylation directe; One-pot; Réactions pallado-catallysées; Indazoles; Suzuki-Miyaura cross-coupling; Direct (hetero)arylation; Direct alkenylation; One-pot; Palladium-catalyzed reactions; 547.59

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APA (6th Edition):

Naas, M. (2016). Synthèse et fonctionnalisation de nouveaux dérivés d’indazoles à visée thérapeutique : Synthesis of new indazoles derivatives with therapeutic potential. (Doctoral Dissertation). Orléans; Université Mohamed V. Retrieved from http://www.theses.fr/2016ORLE2009

Chicago Manual of Style (16th Edition):

Naas, Mohammed. “Synthèse et fonctionnalisation de nouveaux dérivés d’indazoles à visée thérapeutique : Synthesis of new indazoles derivatives with therapeutic potential.” 2016. Doctoral Dissertation, Orléans; Université Mohamed V. Accessed January 26, 2021. http://www.theses.fr/2016ORLE2009.

MLA Handbook (7th Edition):

Naas, Mohammed. “Synthèse et fonctionnalisation de nouveaux dérivés d’indazoles à visée thérapeutique : Synthesis of new indazoles derivatives with therapeutic potential.” 2016. Web. 26 Jan 2021.

Vancouver:

Naas M. Synthèse et fonctionnalisation de nouveaux dérivés d’indazoles à visée thérapeutique : Synthesis of new indazoles derivatives with therapeutic potential. [Internet] [Doctoral dissertation]. Orléans; Université Mohamed V; 2016. [cited 2021 Jan 26]. Available from: http://www.theses.fr/2016ORLE2009.

Council of Science Editors:

Naas M. Synthèse et fonctionnalisation de nouveaux dérivés d’indazoles à visée thérapeutique : Synthesis of new indazoles derivatives with therapeutic potential. [Doctoral Dissertation]. Orléans; Université Mohamed V; 2016. Available from: http://www.theses.fr/2016ORLE2009

22. Da Costa, Laurène. Pharmacochimie de nouveaux inhibiteurs contre les infections à rhinovirus : Pharmacochemistry of new inhibitors against rhinovirus infections.

Degree: Docteur es, Sciences Chimiques, 2017, Aix Marseille Université

Le rhinovirus (RV) est connu pour être l'étiologie de plus de la moitié des rhumes bénins. Ces virus ont également été associés à des pathologies… (more)

Subjects/Keywords: Rhinovirus; Capsid-Binder; Réaction par transfert monoélectronique; Tdae; Couplages pallado-Catalysés; Méthode de Mosher; Rhinovirus; Capsid-Binder; Single electron transfer (SET) reaction; Tdae; Pallado-Catalyzed cross-Coupling reactions; Mosher’s method

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APA (6th Edition):

Da Costa, L. (2017). Pharmacochimie de nouveaux inhibiteurs contre les infections à rhinovirus : Pharmacochemistry of new inhibitors against rhinovirus infections. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2017AIXM0350

Chicago Manual of Style (16th Edition):

Da Costa, Laurène. “Pharmacochimie de nouveaux inhibiteurs contre les infections à rhinovirus : Pharmacochemistry of new inhibitors against rhinovirus infections.” 2017. Doctoral Dissertation, Aix Marseille Université. Accessed January 26, 2021. http://www.theses.fr/2017AIXM0350.

MLA Handbook (7th Edition):

Da Costa, Laurène. “Pharmacochimie de nouveaux inhibiteurs contre les infections à rhinovirus : Pharmacochemistry of new inhibitors against rhinovirus infections.” 2017. Web. 26 Jan 2021.

Vancouver:

Da Costa L. Pharmacochimie de nouveaux inhibiteurs contre les infections à rhinovirus : Pharmacochemistry of new inhibitors against rhinovirus infections. [Internet] [Doctoral dissertation]. Aix Marseille Université 2017. [cited 2021 Jan 26]. Available from: http://www.theses.fr/2017AIXM0350.

Council of Science Editors:

Da Costa L. Pharmacochimie de nouveaux inhibiteurs contre les infections à rhinovirus : Pharmacochemistry of new inhibitors against rhinovirus infections. [Doctoral Dissertation]. Aix Marseille Université 2017. Available from: http://www.theses.fr/2017AIXM0350


Université de Bordeaux I

23. Pradhan, Anirban. Distorted arenes by Scholl cyclizations, towards twisted carbon nanoribbons : Synthèse de composés aromatiques polycycliques distordus par réaction de Scholl vers des nanorubans de carbone courbés.

Degree: Docteur es, Chimie, 2013, Université de Bordeaux I

Les nanorubans de carbone présentent aujourd’hui un grand intérêt en tant que segments de graphène aux propriétés électroniques modulables. Alors que des techniques de synthèse… (more)

Subjects/Keywords: Composés aromatiques polycycliques; Nanorubans de carbone; Hélicènes; Réaction de Scholl; Réactions catalysées de couplages croisés; Polycyclic aromatic compounds (PAC); Carbon nanoribbons; Helicenes; Scholl reaction; Catalyzed cross-coupling reactions

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Pradhan, A. (2013). Distorted arenes by Scholl cyclizations, towards twisted carbon nanoribbons : Synthèse de composés aromatiques polycycliques distordus par réaction de Scholl vers des nanorubans de carbone courbés. (Doctoral Dissertation). Université de Bordeaux I. Retrieved from http://www.theses.fr/2013BOR14849

Chicago Manual of Style (16th Edition):

Pradhan, Anirban. “Distorted arenes by Scholl cyclizations, towards twisted carbon nanoribbons : Synthèse de composés aromatiques polycycliques distordus par réaction de Scholl vers des nanorubans de carbone courbés.” 2013. Doctoral Dissertation, Université de Bordeaux I. Accessed January 26, 2021. http://www.theses.fr/2013BOR14849.

MLA Handbook (7th Edition):

Pradhan, Anirban. “Distorted arenes by Scholl cyclizations, towards twisted carbon nanoribbons : Synthèse de composés aromatiques polycycliques distordus par réaction de Scholl vers des nanorubans de carbone courbés.” 2013. Web. 26 Jan 2021.

Vancouver:

Pradhan A. Distorted arenes by Scholl cyclizations, towards twisted carbon nanoribbons : Synthèse de composés aromatiques polycycliques distordus par réaction de Scholl vers des nanorubans de carbone courbés. [Internet] [Doctoral dissertation]. Université de Bordeaux I; 2013. [cited 2021 Jan 26]. Available from: http://www.theses.fr/2013BOR14849.

Council of Science Editors:

Pradhan A. Distorted arenes by Scholl cyclizations, towards twisted carbon nanoribbons : Synthèse de composés aromatiques polycycliques distordus par réaction de Scholl vers des nanorubans de carbone courbés. [Doctoral Dissertation]. Université de Bordeaux I; 2013. Available from: http://www.theses.fr/2013BOR14849


Université Paris-Sud – Paris XI

24. Soussi, Mohamed Ali. Isocombrétastatine A-4 : métabolisme, synthèse et propriétés antitumorales de nouveaux analogues azotés : Isocombretastatin A-4 : metabolism, synthesis and antithumoral activities of new analogs.

Degree: Docteur es, Chimie pharmaceutique, 2013, Université Paris-Sud – Paris XI

La combrétastatine A-4 (CA-4) est une molécule naturelle qui perturbe sélectivement la vascularisation tumorale en se fixant sur la tubuline. Ce composé sous sa forme… (more)

Subjects/Keywords: Isocombrétastatine A-4; Métabolisme; Inhibition de la polymérisation de la tubuline; Stratégie antivasculaire; Couplages organométalliques; Isocombretastatin A-4; Metabolism; Tubulin polymerization inhibition; Antivascular; Pallado-catalyzed cross coupling

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APA (6th Edition):

Soussi, M. A. (2013). Isocombrétastatine A-4 : métabolisme, synthèse et propriétés antitumorales de nouveaux analogues azotés : Isocombretastatin A-4 : metabolism, synthesis and antithumoral activities of new analogs. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2013PA114801

Chicago Manual of Style (16th Edition):

Soussi, Mohamed Ali. “Isocombrétastatine A-4 : métabolisme, synthèse et propriétés antitumorales de nouveaux analogues azotés : Isocombretastatin A-4 : metabolism, synthesis and antithumoral activities of new analogs.” 2013. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed January 26, 2021. http://www.theses.fr/2013PA114801.

MLA Handbook (7th Edition):

Soussi, Mohamed Ali. “Isocombrétastatine A-4 : métabolisme, synthèse et propriétés antitumorales de nouveaux analogues azotés : Isocombretastatin A-4 : metabolism, synthesis and antithumoral activities of new analogs.” 2013. Web. 26 Jan 2021.

Vancouver:

Soussi MA. Isocombrétastatine A-4 : métabolisme, synthèse et propriétés antitumorales de nouveaux analogues azotés : Isocombretastatin A-4 : metabolism, synthesis and antithumoral activities of new analogs. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2013. [cited 2021 Jan 26]. Available from: http://www.theses.fr/2013PA114801.

Council of Science Editors:

Soussi MA. Isocombrétastatine A-4 : métabolisme, synthèse et propriétés antitumorales de nouveaux analogues azotés : Isocombretastatin A-4 : metabolism, synthesis and antithumoral activities of new analogs. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2013. Available from: http://www.theses.fr/2013PA114801


Université Paris-Sud – Paris XI

25. Tréguier, Bret. Développement de nouveaux analogues structuraux de l’isocombrétastatine A-4 : conception, synthèse et évaluation biologique : Development of news isocombretastatin A-4 derivatives : design, synthesis and biological evaluation.

Degree: Docteur es, Chimie, 2012, Université Paris-Sud – Paris XI

Lors de son développement, une tumeur ne peut survivre sans passer par une étape invasive afin de subvenir à ses besoins en nutriment et en… (more)

Subjects/Keywords: Antivasculaire; Inhibition de la polymérisation de la tubuline; Bioisostérie; Couplage pallado-catalysé; Cyclisation; Ényne; Combretastatin A-4; Antivascular; Cytotoxicity; Tubulin polymerization inhibition; Bioisosterism; Pallado-catalyzed cross coupling; Cyclization; Enyne

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Tréguier, B. (2012). Développement de nouveaux analogues structuraux de l’isocombrétastatine A-4 : conception, synthèse et évaluation biologique : Development of news isocombretastatin A-4 derivatives : design, synthesis and biological evaluation. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2012PA114805

Chicago Manual of Style (16th Edition):

Tréguier, Bret. “Développement de nouveaux analogues structuraux de l’isocombrétastatine A-4 : conception, synthèse et évaluation biologique : Development of news isocombretastatin A-4 derivatives : design, synthesis and biological evaluation.” 2012. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed January 26, 2021. http://www.theses.fr/2012PA114805.

MLA Handbook (7th Edition):

Tréguier, Bret. “Développement de nouveaux analogues structuraux de l’isocombrétastatine A-4 : conception, synthèse et évaluation biologique : Development of news isocombretastatin A-4 derivatives : design, synthesis and biological evaluation.” 2012. Web. 26 Jan 2021.

Vancouver:

Tréguier B. Développement de nouveaux analogues structuraux de l’isocombrétastatine A-4 : conception, synthèse et évaluation biologique : Development of news isocombretastatin A-4 derivatives : design, synthesis and biological evaluation. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2012. [cited 2021 Jan 26]. Available from: http://www.theses.fr/2012PA114805.

Council of Science Editors:

Tréguier B. Développement de nouveaux analogues structuraux de l’isocombrétastatine A-4 : conception, synthèse et évaluation biologique : Development of news isocombretastatin A-4 derivatives : design, synthesis and biological evaluation. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2012. Available from: http://www.theses.fr/2012PA114805

26. LeBlond, Carl. Scope and Mechanistic Studies of the Palladium on Carbon Catalyzed Suzuki Cross Coupling Reaction.

Degree: PhD, Chemistry, 2011, Seton Hall University

Subjects/Keywords: Cross coupling; palladium catalyzed; pallium on carbon; Chemistry; Organic Chemistry

…PdIC Catalyzed Suzuki Cross-Coupling with Aryl Bromides… …69 PdIC Catalyzed Suzuki Cross-Coupling with Aryl Chlorides… …45 Table 3 . Pd/C catalyzed Suzuki cross-coupling results reported by Buchecker et a1… …of the Suzuki Cross-Coupling Reaction… …55 Scope of the Pd/C Suzuki Cross-Coupling… 

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

LeBlond, C. (2011). Scope and Mechanistic Studies of the Palladium on Carbon Catalyzed Suzuki Cross Coupling Reaction. (Doctoral Dissertation). Seton Hall University. Retrieved from https://scholarship.shu.edu/dissertations/1242

Chicago Manual of Style (16th Edition):

LeBlond, Carl. “Scope and Mechanistic Studies of the Palladium on Carbon Catalyzed Suzuki Cross Coupling Reaction.” 2011. Doctoral Dissertation, Seton Hall University. Accessed January 26, 2021. https://scholarship.shu.edu/dissertations/1242.

MLA Handbook (7th Edition):

LeBlond, Carl. “Scope and Mechanistic Studies of the Palladium on Carbon Catalyzed Suzuki Cross Coupling Reaction.” 2011. Web. 26 Jan 2021.

Vancouver:

LeBlond C. Scope and Mechanistic Studies of the Palladium on Carbon Catalyzed Suzuki Cross Coupling Reaction. [Internet] [Doctoral dissertation]. Seton Hall University; 2011. [cited 2021 Jan 26]. Available from: https://scholarship.shu.edu/dissertations/1242.

Council of Science Editors:

LeBlond C. Scope and Mechanistic Studies of the Palladium on Carbon Catalyzed Suzuki Cross Coupling Reaction. [Doctoral Dissertation]. Seton Hall University; 2011. Available from: https://scholarship.shu.edu/dissertations/1242


University of Ottawa

27. Masson-Makdissi, Jeanne. Controlling Selectivity in Cross-Coupling Reactions with Ester Electrophiles .

Degree: 2018, University of Ottawa

 First popularized in the 1970s, transition metal-catalyzed cross-couplings now constitute staple reactions for the formation of carbon-carbon and carbon-heteroatom bonds. Recent endeavours in the field… (more)

Subjects/Keywords: cross-coupling; esters

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APA (6th Edition):

Masson-Makdissi, J. (2018). Controlling Selectivity in Cross-Coupling Reactions with Ester Electrophiles . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/38398

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Masson-Makdissi, Jeanne. “Controlling Selectivity in Cross-Coupling Reactions with Ester Electrophiles .” 2018. Thesis, University of Ottawa. Accessed January 26, 2021. http://hdl.handle.net/10393/38398.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Masson-Makdissi, Jeanne. “Controlling Selectivity in Cross-Coupling Reactions with Ester Electrophiles .” 2018. Web. 26 Jan 2021.

Vancouver:

Masson-Makdissi J. Controlling Selectivity in Cross-Coupling Reactions with Ester Electrophiles . [Internet] [Thesis]. University of Ottawa; 2018. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/10393/38398.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Masson-Makdissi J. Controlling Selectivity in Cross-Coupling Reactions with Ester Electrophiles . [Thesis]. University of Ottawa; 2018. Available from: http://hdl.handle.net/10393/38398

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Illinois – Urbana-Champaign

28. Yousaf, Zain. Development of organosilicon cross-coupling reaction.

Degree: MS, Chemistry, 2015, University of Illinois – Urbana-Champaign

 Use of palladium catalyzed cross-couplings have found widespread use in the pharmaceutical industry and there is a significant ongoing effort to either improve or devise… (more)

Subjects/Keywords: silanolate; cross-coupling

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APA (6th Edition):

Yousaf, Z. (2015). Development of organosilicon cross-coupling reaction. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/89275

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Yousaf, Zain. “Development of organosilicon cross-coupling reaction.” 2015. Thesis, University of Illinois – Urbana-Champaign. Accessed January 26, 2021. http://hdl.handle.net/2142/89275.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Yousaf, Zain. “Development of organosilicon cross-coupling reaction.” 2015. Web. 26 Jan 2021.

Vancouver:

Yousaf Z. Development of organosilicon cross-coupling reaction. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2015. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/2142/89275.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Yousaf Z. Development of organosilicon cross-coupling reaction. [Thesis]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/89275

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

29. Allouch, Fatima. Synthèse et applications de nouveaux complexes métallocéniques multidentes : Synthesis and applications of new multidentate metallocenic complexes.

Degree: Docteur es, Chimie, 2013, Dijon; Université libanaise

Ce mémoire porte sur l’accès simple et peu coûteux à de nouveaux ligands ferrocéniques aminés et aminophosphinés et leur coordination avec des métaux de transition… (more)

Subjects/Keywords: Métallo-ligands ferrocéniques aminés et aminophosphinés; Palladation; Amination réductrice; Ligands hybrides (N,P); Réaction de couplage carbone-carbone; Suzuki; Sonogashira; Amino and aminophosphine ferrocenyl metallo-ligand; Palladation; Reductive amination; N,P hybrid ligands; C-C cross-coupling reaction; Suzuki; Sonogashira; 541.2; 541.39; 547

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APA (6th Edition):

Allouch, F. (2013). Synthèse et applications de nouveaux complexes métallocéniques multidentes : Synthesis and applications of new multidentate metallocenic complexes. (Doctoral Dissertation). Dijon; Université libanaise. Retrieved from http://www.theses.fr/2013DIJOS002

Chicago Manual of Style (16th Edition):

Allouch, Fatima. “Synthèse et applications de nouveaux complexes métallocéniques multidentes : Synthesis and applications of new multidentate metallocenic complexes.” 2013. Doctoral Dissertation, Dijon; Université libanaise. Accessed January 26, 2021. http://www.theses.fr/2013DIJOS002.

MLA Handbook (7th Edition):

Allouch, Fatima. “Synthèse et applications de nouveaux complexes métallocéniques multidentes : Synthesis and applications of new multidentate metallocenic complexes.” 2013. Web. 26 Jan 2021.

Vancouver:

Allouch F. Synthèse et applications de nouveaux complexes métallocéniques multidentes : Synthesis and applications of new multidentate metallocenic complexes. [Internet] [Doctoral dissertation]. Dijon; Université libanaise; 2013. [cited 2021 Jan 26]. Available from: http://www.theses.fr/2013DIJOS002.

Council of Science Editors:

Allouch F. Synthèse et applications de nouveaux complexes métallocéniques multidentes : Synthesis and applications of new multidentate metallocenic complexes. [Doctoral Dissertation]. Dijon; Université libanaise; 2013. Available from: http://www.theses.fr/2013DIJOS002


NSYSU

30. Chiang, Meng-fan. Palladium-Catalyzed Direct Ortho-Aroylation of N-Arylpyridin-2-amines with Aldehydes via C-H Activation.

Degree: Master, Chemistry, 2015, NSYSU

 A direct ortho-aroylation of N-arylpyridin-2-amines with aldehydes to afford mono- and di-aroylated N-arylpyridin-2-amines in modest to good yields is presented. In the reaction, palladium(II) acetate,… (more)

Subjects/Keywords: palladium; C-C coupling; C-H activation; catalyzed reaction; ortho-aroylation

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APA (6th Edition):

Chiang, M. (2015). Palladium-Catalyzed Direct Ortho-Aroylation of N-Arylpyridin-2-amines with Aldehydes via C-H Activation. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0604115-140952

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Chiang, Meng-fan. “Palladium-Catalyzed Direct Ortho-Aroylation of N-Arylpyridin-2-amines with Aldehydes via C-H Activation.” 2015. Thesis, NSYSU. Accessed January 26, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0604115-140952.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Chiang, Meng-fan. “Palladium-Catalyzed Direct Ortho-Aroylation of N-Arylpyridin-2-amines with Aldehydes via C-H Activation.” 2015. Web. 26 Jan 2021.

Vancouver:

Chiang M. Palladium-Catalyzed Direct Ortho-Aroylation of N-Arylpyridin-2-amines with Aldehydes via C-H Activation. [Internet] [Thesis]. NSYSU; 2015. [cited 2021 Jan 26]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0604115-140952.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Chiang M. Palladium-Catalyzed Direct Ortho-Aroylation of N-Arylpyridin-2-amines with Aldehydes via C-H Activation. [Thesis]. NSYSU; 2015. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0604115-140952

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

[1] [2] [3] [4] [5] … [459]

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