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You searched for subject:(Palladium catalyzed cross coupling reaction). Showing records 1 – 30 of 21530 total matches.

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NSYSU

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

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


NSYSU

2. Chen, Jiun-hong. Palladium-Catalyzed Direct Carbon-Hydrogen Activation Reaction to 1-methyl-N-phenyl-1H-indole-3-carboxamide to 11-methyl-5H-indolo[3,2-c]quinolin-6(11H)-one.

Degree: Master, Chemistry, 2016, NSYSU

 A direct ortho-Arylation of 1-methyl-N-phenyl-1H-indole-3-carboxamide via Carbon-Hydride Bond Activation. In the reaction, Palladium(II) trifluoroacetate, Copper(II) acetate, Potassium phosphate, Pivalic acid, and DMF:1,4-Dioxane=1/9 were used as… (more)

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

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APA (6th Edition):

Chen, J. (2016). Palladium-Catalyzed Direct Carbon-Hydrogen Activation Reaction to 1-methyl-N-phenyl-1H-indole-3-carboxamide to 11-methyl-5H-indolo[3,2-c]quinolin-6(11H)-one. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0618116-111826

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):

Chen, Jiun-hong. “Palladium-Catalyzed Direct Carbon-Hydrogen Activation Reaction to 1-methyl-N-phenyl-1H-indole-3-carboxamide to 11-methyl-5H-indolo[3,2-c]quinolin-6(11H)-one.” 2016. Thesis, NSYSU. Accessed January 26, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0618116-111826.

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

MLA Handbook (7th Edition):

Chen, Jiun-hong. “Palladium-Catalyzed Direct Carbon-Hydrogen Activation Reaction to 1-methyl-N-phenyl-1H-indole-3-carboxamide to 11-methyl-5H-indolo[3,2-c]quinolin-6(11H)-one.” 2016. Web. 26 Jan 2021.

Vancouver:

Chen J. Palladium-Catalyzed Direct Carbon-Hydrogen Activation Reaction to 1-methyl-N-phenyl-1H-indole-3-carboxamide to 11-methyl-5H-indolo[3,2-c]quinolin-6(11H)-one. [Internet] [Thesis]. NSYSU; 2016. [cited 2021 Jan 26]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0618116-111826.

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

Council of Science Editors:

Chen J. Palladium-Catalyzed Direct Carbon-Hydrogen Activation Reaction to 1-methyl-N-phenyl-1H-indole-3-carboxamide to 11-methyl-5H-indolo[3,2-c]quinolin-6(11H)-one. [Thesis]. NSYSU; 2016. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0618116-111826

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


University of Illinois – Urbana-Champaign

3. 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 Paris-Sud – Paris XI

4. 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

5. Geogheghan, Katherine Jayne. Boronic acid speciation in Suzuki-Miyaura cross-coupling.

Degree: PhD, 2018, University of Edinburgh

 Since its discovery in 1979, the Suzuki-Miyaura (SM) reaction has become one of the most widely utilised tools for carbon-carbon bond formation. The palladium catalysed… (more)

Subjects/Keywords: 660; cross-coupling; Suzuki-Miyaura reaction; palladium catalysed coupling; boronic esters

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APA (6th Edition):

Geogheghan, K. J. (2018). Boronic acid speciation in Suzuki-Miyaura cross-coupling. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/33092

Chicago Manual of Style (16th Edition):

Geogheghan, Katherine Jayne. “Boronic acid speciation in Suzuki-Miyaura cross-coupling.” 2018. Doctoral Dissertation, University of Edinburgh. Accessed January 26, 2021. http://hdl.handle.net/1842/33092.

MLA Handbook (7th Edition):

Geogheghan, Katherine Jayne. “Boronic acid speciation in Suzuki-Miyaura cross-coupling.” 2018. Web. 26 Jan 2021.

Vancouver:

Geogheghan KJ. Boronic acid speciation in Suzuki-Miyaura cross-coupling. [Internet] [Doctoral dissertation]. University of Edinburgh; 2018. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/1842/33092.

Council of Science Editors:

Geogheghan KJ. Boronic acid speciation in Suzuki-Miyaura cross-coupling. [Doctoral Dissertation]. University of Edinburgh; 2018. Available from: http://hdl.handle.net/1842/33092


University of Washington

6. 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

7. 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


University of Illinois – Chicago

8. 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

9. Urgin, Karene. Préparation de dérivés aryl- et hétéroaryl- pyridazine(s) par voies organométalliques chimiques ou électrochimiques : Preparation of heteroaryl and aryl pyridazine derivatives by organometallic.

Degree: Docteur es, Chimie organique, minérale, industrielle, 2010, Université Paris-Est

Les hétérocycles aromatiques sont des motifs structuraux rencontrés dans un grand nombre de substances d'intérêts biologiques ou pharmacologiques. Plus particulièrement, les pyridazines substituées font l'objet… (more)

Subjects/Keywords: Pyridazine; Couplage; Electrosynthèse; Organozinciques; Triarylbismuths; Palladium; Pyridazine; Cross-coupling reaction; Electrosynthesis; Organozinc compounds; Triarylbismuths; Palladium

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APA (6th Edition):

Urgin, K. (2010). Préparation de dérivés aryl- et hétéroaryl- pyridazine(s) par voies organométalliques chimiques ou électrochimiques : Preparation of heteroaryl and aryl pyridazine derivatives by organometallic. (Doctoral Dissertation). Université Paris-Est. Retrieved from http://www.theses.fr/2010PEST1094

Chicago Manual of Style (16th Edition):

Urgin, Karene. “Préparation de dérivés aryl- et hétéroaryl- pyridazine(s) par voies organométalliques chimiques ou électrochimiques : Preparation of heteroaryl and aryl pyridazine derivatives by organometallic.” 2010. Doctoral Dissertation, Université Paris-Est. Accessed January 26, 2021. http://www.theses.fr/2010PEST1094.

MLA Handbook (7th Edition):

Urgin, Karene. “Préparation de dérivés aryl- et hétéroaryl- pyridazine(s) par voies organométalliques chimiques ou électrochimiques : Preparation of heteroaryl and aryl pyridazine derivatives by organometallic.” 2010. Web. 26 Jan 2021.

Vancouver:

Urgin K. Préparation de dérivés aryl- et hétéroaryl- pyridazine(s) par voies organométalliques chimiques ou électrochimiques : Preparation of heteroaryl and aryl pyridazine derivatives by organometallic. [Internet] [Doctoral dissertation]. Université Paris-Est; 2010. [cited 2021 Jan 26]. Available from: http://www.theses.fr/2010PEST1094.

Council of Science Editors:

Urgin K. Préparation de dérivés aryl- et hétéroaryl- pyridazine(s) par voies organométalliques chimiques ou électrochimiques : Preparation of heteroaryl and aryl pyridazine derivatives by organometallic. [Doctoral Dissertation]. Université Paris-Est; 2010. Available from: http://www.theses.fr/2010PEST1094


University of Alberta

10. 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


McMaster University

11. 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


Florida International University

12. 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

13. 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

14. 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


NSYSU

15. Huang, Hao-ping. Palladium(II)-Catalyzed Direct Ortho Arylation of 4-Methyl-N-phenylpyridin-2-amines via Suzuki-Miyaura Type C-H Bond Activation/C-C Bond Coupling.

Degree: Master, Chemistry, 2013, NSYSU

 The direct ortho arylation of 4-methyl-N-phenylpyridin-2-amines via palladium(II)-catalyzed C-H activation is described. Treatment of 4-methyl-N-phenylpyridin-2-amine with potassium aryltrifluoroborate using ten mol % of Pd(OAc)2 as… (more)

Subjects/Keywords: palladium; C-H bond activation; potassium aryltrifluoroborate; Suzuki-Miyaura cross-coupling reaction

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APA (6th Edition):

Huang, H. (2013). Palladium(II)-Catalyzed Direct Ortho Arylation of 4-Methyl-N-phenylpyridin-2-amines via Suzuki-Miyaura Type C-H Bond Activation/C-C Bond Coupling. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0406113-201051

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):

Huang, Hao-ping. “Palladium(II)-Catalyzed Direct Ortho Arylation of 4-Methyl-N-phenylpyridin-2-amines via Suzuki-Miyaura Type C-H Bond Activation/C-C Bond Coupling.” 2013. Thesis, NSYSU. Accessed January 26, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0406113-201051.

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

MLA Handbook (7th Edition):

Huang, Hao-ping. “Palladium(II)-Catalyzed Direct Ortho Arylation of 4-Methyl-N-phenylpyridin-2-amines via Suzuki-Miyaura Type C-H Bond Activation/C-C Bond Coupling.” 2013. Web. 26 Jan 2021.

Vancouver:

Huang H. Palladium(II)-Catalyzed Direct Ortho Arylation of 4-Methyl-N-phenylpyridin-2-amines via Suzuki-Miyaura Type C-H Bond Activation/C-C Bond Coupling. [Internet] [Thesis]. NSYSU; 2013. [cited 2021 Jan 26]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0406113-201051.

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

Council of Science Editors:

Huang H. Palladium(II)-Catalyzed Direct Ortho Arylation of 4-Methyl-N-phenylpyridin-2-amines via Suzuki-Miyaura Type C-H Bond Activation/C-C Bond Coupling. [Thesis]. NSYSU; 2013. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0406113-201051

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

16. Souffrin, Agathe. Conception, synthèse et évaluation pharmacologique de maléimides, inhibiteurs potentiels de l'intégrase du VIH-1 : Design, synthesis and pharmacological evaluation of maleimides, potential inhibitors of HIV-1 integrase.

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

Notre équipe de recherche a récemment développé les premiers inhibiteurs d’une enzyme à DDE, la transposase MOS1, une enzyme analogue à l’intégrase du VIH-1. Ces… (more)

Subjects/Keywords: SIDA; VIH; Intégrase; Enzyme à DDE; Transposase; Inhibiteur; Maléimide; Pharmacomodulation; Synthèse multi-étape; Chimie hétérocyclique; Réaction de couplage pallado-catalysée; Modélisation moléculaire; Complexation; Évaluation pharmacologique; Photoactivation; AIDS; HIV; Integrase; DDE enzyme; Transposase; Inhibitor; Maleimide; Pharmacomodulation; Multi-step synthesis; Heterocyclic chemistry; Palladium-catalyzed cross-coupling reaction; Molecular modeling; Complexation; Pharmacological evaluation; Photoaffinity labeling

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APA (6th Edition):

Souffrin, A. (2012). Conception, synthèse et évaluation pharmacologique de maléimides, inhibiteurs potentiels de l'intégrase du VIH-1 : Design, synthesis and pharmacological evaluation of maleimides, potential inhibitors of HIV-1 integrase. (Doctoral Dissertation). Université François-Rabelais de Tours. Retrieved from http://www.theses.fr/2012TOUR3801

Chicago Manual of Style (16th Edition):

Souffrin, Agathe. “Conception, synthèse et évaluation pharmacologique de maléimides, inhibiteurs potentiels de l'intégrase du VIH-1 : Design, synthesis and pharmacological evaluation of maleimides, potential inhibitors of HIV-1 integrase.” 2012. Doctoral Dissertation, Université François-Rabelais de Tours. Accessed January 26, 2021. http://www.theses.fr/2012TOUR3801.

MLA Handbook (7th Edition):

Souffrin, Agathe. “Conception, synthèse et évaluation pharmacologique de maléimides, inhibiteurs potentiels de l'intégrase du VIH-1 : Design, synthesis and pharmacological evaluation of maleimides, potential inhibitors of HIV-1 integrase.” 2012. Web. 26 Jan 2021.

Vancouver:

Souffrin A. Conception, synthèse et évaluation pharmacologique de maléimides, inhibiteurs potentiels de l'intégrase du VIH-1 : Design, synthesis and pharmacological evaluation of maleimides, potential inhibitors of HIV-1 integrase. [Internet] [Doctoral dissertation]. Université François-Rabelais de Tours; 2012. [cited 2021 Jan 26]. Available from: http://www.theses.fr/2012TOUR3801.

Council of Science Editors:

Souffrin A. Conception, synthèse et évaluation pharmacologique de maléimides, inhibiteurs potentiels de l'intégrase du VIH-1 : Design, synthesis and pharmacological evaluation of maleimides, potential inhibitors of HIV-1 integrase. [Doctoral Dissertation]. Université François-Rabelais de Tours; 2012. Available from: http://www.theses.fr/2012TOUR3801

17. 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

18. 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

…of the Suzuki Cross-Coupling Reaction… …PdIC Catalyzed Suzuki Cross-Coupling with Aryl Bromides… …69 PdIC Catalyzed Suzuki Cross-Coupling with Aryl Chlorides… …62 Figure 10. Hammett plot for the heterogeneous Suzuki cross-coupling reaction using Pd/C… …45 Table 3 . Pd/C catalyzed Suzuki cross-coupling results reported by Buchecker et a1… 

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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

19. Charpenay, Mélanie. Fenestradiènes et cyclooctatriènes : synthèse directe par réaction en cascade palladocatalysée : Fenestradienes and cyclooctatrienes : direct synthesis using a palladium-catalyzed cascade reaction.

Degree: Docteur es, Chimie, 2012, Université de Strasbourg

Ces travaux de thèse nous ont permis de mettre au point différentes voies de synthèse de systèmes polycycliques complexes tels que des fenestradiènes et des… (more)

Subjects/Keywords: Fenestrane; Cyclooctatriene; Réaction en cascade; Catalyse au palladium; Fenestradienes; Cyclooctatrienes; Cascade reaction; Palladium-catalyzed; 541.39

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APA (6th Edition):

Charpenay, M. (2012). Fenestradiènes et cyclooctatriènes : synthèse directe par réaction en cascade palladocatalysée : Fenestradienes and cyclooctatrienes : direct synthesis using a palladium-catalyzed cascade reaction. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2012STRAF040

Chicago Manual of Style (16th Edition):

Charpenay, Mélanie. “Fenestradiènes et cyclooctatriènes : synthèse directe par réaction en cascade palladocatalysée : Fenestradienes and cyclooctatrienes : direct synthesis using a palladium-catalyzed cascade reaction.” 2012. Doctoral Dissertation, Université de Strasbourg. Accessed January 26, 2021. http://www.theses.fr/2012STRAF040.

MLA Handbook (7th Edition):

Charpenay, Mélanie. “Fenestradiènes et cyclooctatriènes : synthèse directe par réaction en cascade palladocatalysée : Fenestradienes and cyclooctatrienes : direct synthesis using a palladium-catalyzed cascade reaction.” 2012. Web. 26 Jan 2021.

Vancouver:

Charpenay M. Fenestradiènes et cyclooctatriènes : synthèse directe par réaction en cascade palladocatalysée : Fenestradienes and cyclooctatrienes : direct synthesis using a palladium-catalyzed cascade reaction. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2012. [cited 2021 Jan 26]. Available from: http://www.theses.fr/2012STRAF040.

Council of Science Editors:

Charpenay M. Fenestradiènes et cyclooctatriènes : synthèse directe par réaction en cascade palladocatalysée : Fenestradienes and cyclooctatrienes : direct synthesis using a palladium-catalyzed cascade reaction. [Doctoral Dissertation]. Université de Strasbourg; 2012. Available from: http://www.theses.fr/2012STRAF040


King Abdullah University of Science and Technology

20. Walter, Philipp E. Optimization of an Efficient and Sustainable Sonogashira Cross-Coupling Protocol.

Degree: 2012, King Abdullah University of Science and Technology

Cross coupling reactions are a well-established tool in modern organic synthesis and play a crucial role in the synthesis of a high number of organic… (more)

Subjects/Keywords: sonogashira; cross-coupling; water; palladium; green

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APA (6th Edition):

Walter, P. E. (2012). Optimization of an Efficient and Sustainable Sonogashira Cross-Coupling Protocol. (Thesis). King Abdullah University of Science and Technology. Retrieved from http://hdl.handle.net/10754/262732

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):

Walter, Philipp E. “Optimization of an Efficient and Sustainable Sonogashira Cross-Coupling Protocol.” 2012. Thesis, King Abdullah University of Science and Technology. Accessed January 26, 2021. http://hdl.handle.net/10754/262732.

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

MLA Handbook (7th Edition):

Walter, Philipp E. “Optimization of an Efficient and Sustainable Sonogashira Cross-Coupling Protocol.” 2012. Web. 26 Jan 2021.

Vancouver:

Walter PE. Optimization of an Efficient and Sustainable Sonogashira Cross-Coupling Protocol. [Internet] [Thesis]. King Abdullah University of Science and Technology; 2012. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/10754/262732.

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

Council of Science Editors:

Walter PE. Optimization of an Efficient and Sustainable Sonogashira Cross-Coupling Protocol. [Thesis]. King Abdullah University of Science and Technology; 2012. Available from: http://hdl.handle.net/10754/262732

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


Boston College

21. Le, Hai. Developments in palladium catalyzed reactions: Strategies to synthesize asymmetric 1,5-dienes and 1,4-dicarbonyls.

Degree: PhD, Chemistry, 2014, Boston College

 This dissertation details recent developments in palladium catalyzed carbon-carbon bond formation reactions with two areas of focus: the palladium catalyzed branched and enantioselective allyl-allyl cross-coupling,… (more)

Subjects/Keywords: allyl; asymmetric; cross-coupling; organometallic; palladium; synthesis

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APA (6th Edition):

Le, H. (2014). Developments in palladium catalyzed reactions: Strategies to synthesize asymmetric 1,5-dienes and 1,4-dicarbonyls. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:104389

Chicago Manual of Style (16th Edition):

Le, Hai. “Developments in palladium catalyzed reactions: Strategies to synthesize asymmetric 1,5-dienes and 1,4-dicarbonyls.” 2014. Doctoral Dissertation, Boston College. Accessed January 26, 2021. http://dlib.bc.edu/islandora/object/bc-ir:104389.

MLA Handbook (7th Edition):

Le, Hai. “Developments in palladium catalyzed reactions: Strategies to synthesize asymmetric 1,5-dienes and 1,4-dicarbonyls.” 2014. Web. 26 Jan 2021.

Vancouver:

Le H. Developments in palladium catalyzed reactions: Strategies to synthesize asymmetric 1,5-dienes and 1,4-dicarbonyls. [Internet] [Doctoral dissertation]. Boston College; 2014. [cited 2021 Jan 26]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:104389.

Council of Science Editors:

Le H. Developments in palladium catalyzed reactions: Strategies to synthesize asymmetric 1,5-dienes and 1,4-dicarbonyls. [Doctoral Dissertation]. Boston College; 2014. Available from: http://dlib.bc.edu/islandora/object/bc-ir:104389


Boston College

22. Edelstein, Emma Kate. Enantioselective synthesis and stereospecific transformations of organoboronic esters.

Degree: PhD, Chemistry, 2018, Boston College

 This dissertation details the development of several enantioselective or stereospecific transformations involving organoboronic esters. Chapter one will introduce electrophile-induced boronate rearrangements which underpins much of… (more)

Subjects/Keywords: Boron; Catalysis; Cross-Coupling; Enantioselective; Palladium; Stereospecific

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APA (6th Edition):

Edelstein, E. K. (2018). Enantioselective synthesis and stereospecific transformations of organoboronic esters. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:108038

Chicago Manual of Style (16th Edition):

Edelstein, Emma Kate. “Enantioselective synthesis and stereospecific transformations of organoboronic esters.” 2018. Doctoral Dissertation, Boston College. Accessed January 26, 2021. http://dlib.bc.edu/islandora/object/bc-ir:108038.

MLA Handbook (7th Edition):

Edelstein, Emma Kate. “Enantioselective synthesis and stereospecific transformations of organoboronic esters.” 2018. Web. 26 Jan 2021.

Vancouver:

Edelstein EK. Enantioselective synthesis and stereospecific transformations of organoboronic esters. [Internet] [Doctoral dissertation]. Boston College; 2018. [cited 2021 Jan 26]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:108038.

Council of Science Editors:

Edelstein EK. Enantioselective synthesis and stereospecific transformations of organoboronic esters. [Doctoral Dissertation]. Boston College; 2018. Available from: http://dlib.bc.edu/islandora/object/bc-ir:108038


Queens University

23. Fraser, Andrew. Investigations of a New and Improved Precataylst for Palladium Catalyzed Cross Coupling Reactions .

Degree: Chemistry, 2013, Queens University

 Little attention has been given to the formation of the putative PdL2 species required for Pd-catalyzed cross-coupling reactions. Active species are generally difficult to store… (more)

Subjects/Keywords: Catalysis ; Palladium ; Cross-Coupling ; Organometallic Chemistry

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APA (6th Edition):

Fraser, A. (2013). Investigations of a New and Improved Precataylst for Palladium Catalyzed Cross Coupling Reactions . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/8094

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):

Fraser, Andrew. “Investigations of a New and Improved Precataylst for Palladium Catalyzed Cross Coupling Reactions .” 2013. Thesis, Queens University. Accessed January 26, 2021. http://hdl.handle.net/1974/8094.

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

MLA Handbook (7th Edition):

Fraser, Andrew. “Investigations of a New and Improved Precataylst for Palladium Catalyzed Cross Coupling Reactions .” 2013. Web. 26 Jan 2021.

Vancouver:

Fraser A. Investigations of a New and Improved Precataylst for Palladium Catalyzed Cross Coupling Reactions . [Internet] [Thesis]. Queens University; 2013. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/1974/8094.

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

Council of Science Editors:

Fraser A. Investigations of a New and Improved Precataylst for Palladium Catalyzed Cross Coupling Reactions . [Thesis]. Queens University; 2013. Available from: http://hdl.handle.net/1974/8094

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

24. Peramo, Arnaud. Modification sélective de protéines en milieu biologique par réaction de Suzuki-Miyaura nanocatalysée : Selective modification of a protein in biological media by nanocatalyzed Suzuki-Miyaura reaction.

Degree: Docteur es, Pharmacotechnie et biopharmacie, 2019, Université Paris-Saclay (ComUE)

Les nanotechnologies ont ouvert de nouvelles perspectives pour l’administration ciblée des médicaments. Les approches actuelles en nanomédecine sont basées sur l’encapsulation d’un principe actif dans… (more)

Subjects/Keywords: Palladium nanoparticules; Réaction de Suzuki-Myaura; Chimie in vivo; Thyroglobuline; Protémoque; Palladium nanoparticles; Suzuki-Myaura cross-Coupling reaction; In vivo chemistry; Thyroglobulin; Proteomic

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

APA (6th Edition):

Peramo, A. (2019). Modification sélective de protéines en milieu biologique par réaction de Suzuki-Miyaura nanocatalysée : Selective modification of a protein in biological media by nanocatalyzed Suzuki-Miyaura reaction. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2019SACLS600

Chicago Manual of Style (16th Edition):

Peramo, Arnaud. “Modification sélective de protéines en milieu biologique par réaction de Suzuki-Miyaura nanocatalysée : Selective modification of a protein in biological media by nanocatalyzed Suzuki-Miyaura reaction.” 2019. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed January 26, 2021. http://www.theses.fr/2019SACLS600.

MLA Handbook (7th Edition):

Peramo, Arnaud. “Modification sélective de protéines en milieu biologique par réaction de Suzuki-Miyaura nanocatalysée : Selective modification of a protein in biological media by nanocatalyzed Suzuki-Miyaura reaction.” 2019. Web. 26 Jan 2021.

Vancouver:

Peramo A. Modification sélective de protéines en milieu biologique par réaction de Suzuki-Miyaura nanocatalysée : Selective modification of a protein in biological media by nanocatalyzed Suzuki-Miyaura reaction. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2019. [cited 2021 Jan 26]. Available from: http://www.theses.fr/2019SACLS600.

Council of Science Editors:

Peramo A. Modification sélective de protéines en milieu biologique par réaction de Suzuki-Miyaura nanocatalysée : Selective modification of a protein in biological media by nanocatalyzed Suzuki-Miyaura reaction. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2019. Available from: http://www.theses.fr/2019SACLS600

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

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

26. 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


University of Gothenburg / Göteborgs Universitet

27. Kleimark, Jonatan. MECHANISTIC INVESTIGATIONS OF TRANSITION METAL CATALYZED REACTIONS.

Degree: 2011, University of Gothenburg / Göteborgs Universitet

 Transition metal catalyzed reactions have had a large impact on the human progress for the last century. Several extremely important areas, such as the agricultural… (more)

Subjects/Keywords: alkene insertion; allylic alkylation; catalysis; cross coupling; density funtional theory; free energy surface; iron; kinetic investigation; Mizoroki-Heck reaction; nickel; palladium; reaction mechanism; sulfinylation; transition metal

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

APA (6th Edition):

Kleimark, J. (2011). MECHANISTIC INVESTIGATIONS OF TRANSITION METAL CATALYZED REACTIONS. (Thesis). University of Gothenburg / Göteborgs Universitet. Retrieved from http://hdl.handle.net/2077/27967

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):

Kleimark, Jonatan. “MECHANISTIC INVESTIGATIONS OF TRANSITION METAL CATALYZED REACTIONS.” 2011. Thesis, University of Gothenburg / Göteborgs Universitet. Accessed January 26, 2021. http://hdl.handle.net/2077/27967.

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

MLA Handbook (7th Edition):

Kleimark, Jonatan. “MECHANISTIC INVESTIGATIONS OF TRANSITION METAL CATALYZED REACTIONS.” 2011. Web. 26 Jan 2021.

Vancouver:

Kleimark J. MECHANISTIC INVESTIGATIONS OF TRANSITION METAL CATALYZED REACTIONS. [Internet] [Thesis]. University of Gothenburg / Göteborgs Universitet; 2011. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/2077/27967.

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

Council of Science Editors:

Kleimark J. MECHANISTIC INVESTIGATIONS OF TRANSITION METAL CATALYZED REACTIONS. [Thesis]. University of Gothenburg / Göteborgs Universitet; 2011. Available from: http://hdl.handle.net/2077/27967

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


University of Rochester

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

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


NSYSU

29. Huang, Nan-Yuan. Development of New Synthesis of Sulfur-oxazoline Ligands.

Degree: Master, Chemistry, 2011, NSYSU

 This thesis is the use of commercially available methyl 2-iodobenzoate as the starting material and was prepared into iodine - oxazoline compound 118. Then, we… (more)

Subjects/Keywords: CuI-catalyzed reaction; Iodooxazoline; Pd-catalyzed asymmetric alkylation; Carbon-sulfur coupling reaction; Chiral sulfur-oxazoline ligands

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

APA (6th Edition):

Huang, N. (2011). Development of New Synthesis of Sulfur-oxazoline Ligands. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-1003111-232108

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):

Huang, Nan-Yuan. “Development of New Synthesis of Sulfur-oxazoline Ligands.” 2011. Thesis, NSYSU. Accessed January 26, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-1003111-232108.

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

MLA Handbook (7th Edition):

Huang, Nan-Yuan. “Development of New Synthesis of Sulfur-oxazoline Ligands.” 2011. Web. 26 Jan 2021.

Vancouver:

Huang N. Development of New Synthesis of Sulfur-oxazoline Ligands. [Internet] [Thesis]. NSYSU; 2011. [cited 2021 Jan 26]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-1003111-232108.

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

Council of Science Editors:

Huang N. Development of New Synthesis of Sulfur-oxazoline Ligands. [Thesis]. NSYSU; 2011. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-1003111-232108

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

30. Gigant, Nicolas. Synthèse et réactivité d'énamides, de la diversité moléculaire à la synthèse de molécules bioactives et/ou naturelles : Synthesis and reactivity of enamides, toward the molecular diversity and the synthesis of bioactive and/or natural compounds.

Degree: Docteur es, Chimie organique, 2012, Université d'Orléans

La nécessité grandissante de disposer d’une large librairie de diverses petites molécules pour le screening biologique constitue une puissante force motrice pour les chimistes organiciens… (more)

Subjects/Keywords: Enamide; Diversité moléculaire; Synthèse orientée vers la diversité; Phosphates vinyliques; Additions d’aza-Michaël; Nitrènes; Réactions de couplage pallado-catalysées; Réactions en cascades; Enamides; Molecular diversity; Diversity-oriented synthesis; Vinylphosphates; Aza-Michael additions; Nitrenes; Palladium-catalyzed cross-coupling reactions; Cascade reactions

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

APA (6th Edition):

Gigant, N. (2012). Synthèse et réactivité d'énamides, de la diversité moléculaire à la synthèse de molécules bioactives et/ou naturelles : Synthesis and reactivity of enamides, toward the molecular diversity and the synthesis of bioactive and/or natural compounds. (Doctoral Dissertation). Université d'Orléans. Retrieved from http://www.theses.fr/2012ORLE2039

Chicago Manual of Style (16th Edition):

Gigant, Nicolas. “Synthèse et réactivité d'énamides, de la diversité moléculaire à la synthèse de molécules bioactives et/ou naturelles : Synthesis and reactivity of enamides, toward the molecular diversity and the synthesis of bioactive and/or natural compounds.” 2012. Doctoral Dissertation, Université d'Orléans. Accessed January 26, 2021. http://www.theses.fr/2012ORLE2039.

MLA Handbook (7th Edition):

Gigant, Nicolas. “Synthèse et réactivité d'énamides, de la diversité moléculaire à la synthèse de molécules bioactives et/ou naturelles : Synthesis and reactivity of enamides, toward the molecular diversity and the synthesis of bioactive and/or natural compounds.” 2012. Web. 26 Jan 2021.

Vancouver:

Gigant N. Synthèse et réactivité d'énamides, de la diversité moléculaire à la synthèse de molécules bioactives et/ou naturelles : Synthesis and reactivity of enamides, toward the molecular diversity and the synthesis of bioactive and/or natural compounds. [Internet] [Doctoral dissertation]. Université d'Orléans; 2012. [cited 2021 Jan 26]. Available from: http://www.theses.fr/2012ORLE2039.

Council of Science Editors:

Gigant N. Synthèse et réactivité d'énamides, de la diversité moléculaire à la synthèse de molécules bioactives et/ou naturelles : Synthesis and reactivity of enamides, toward the molecular diversity and the synthesis of bioactive and/or natural compounds. [Doctoral Dissertation]. Université d'Orléans; 2012. Available from: http://www.theses.fr/2012ORLE2039

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