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You searched for subject:(Cross coupling reaction). Showing records 1 – 30 of 51 total matches.

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1. 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 March 04, 2021. http://hdl.handle.net/1842/33092.

MLA Handbook (7th Edition):

Geogheghan, Katherine Jayne. “Boronic acid speciation in Suzuki-Miyaura cross-coupling.” 2018. Web. 04 Mar 2021.

Vancouver:

Geogheghan KJ. Boronic acid speciation in Suzuki-Miyaura cross-coupling. [Internet] [Doctoral dissertation]. University of Edinburgh; 2018. [cited 2021 Mar 04]. 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 Arizona

2. Bell, Christan Elizabeth. Synthesis and Reactivity of New Organoboron Reagents and Development of New Methodologies for the Generation of Novel Drug-Like Scaffolds .

Degree: 2012, University of Arizona

 This research focused on the synthesis of novel ogranoboron reagents in efforts to perform a variety of synthetic transformations, and additionally, the development of new… (more)

Subjects/Keywords: multicomponent reaction; Chemistry; cross-coupling; Frustrated Lewis pairs

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APA (6th Edition):

Bell, C. E. (2012). Synthesis and Reactivity of New Organoboron Reagents and Development of New Methodologies for the Generation of Novel Drug-Like Scaffolds . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/265557

Chicago Manual of Style (16th Edition):

Bell, Christan Elizabeth. “Synthesis and Reactivity of New Organoboron Reagents and Development of New Methodologies for the Generation of Novel Drug-Like Scaffolds .” 2012. Doctoral Dissertation, University of Arizona. Accessed March 04, 2021. http://hdl.handle.net/10150/265557.

MLA Handbook (7th Edition):

Bell, Christan Elizabeth. “Synthesis and Reactivity of New Organoboron Reagents and Development of New Methodologies for the Generation of Novel Drug-Like Scaffolds .” 2012. Web. 04 Mar 2021.

Vancouver:

Bell CE. Synthesis and Reactivity of New Organoboron Reagents and Development of New Methodologies for the Generation of Novel Drug-Like Scaffolds . [Internet] [Doctoral dissertation]. University of Arizona; 2012. [cited 2021 Mar 04]. Available from: http://hdl.handle.net/10150/265557.

Council of Science Editors:

Bell CE. Synthesis and Reactivity of New Organoboron Reagents and Development of New Methodologies for the Generation of Novel Drug-Like Scaffolds . [Doctoral Dissertation]. University of Arizona; 2012. Available from: http://hdl.handle.net/10150/265557


University of Edinburgh

3. Corrie, Thomas James Alexander. Intramolecular direct arylation.

Degree: PhD, 2017, University of Edinburgh

 The research conducted for this thesis has led to the development of an intramolecular gold-catalysed direct arylation protocol whereby tethered arenes and aryltrimethylsilanes are coupled… (more)

Subjects/Keywords: gold-catalysis; cross-coupling; intermolecular reaction; tethered arenes; aryltrimethylsilanes

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APA (6th Edition):

Corrie, T. J. A. (2017). Intramolecular direct arylation. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/28820

Chicago Manual of Style (16th Edition):

Corrie, Thomas James Alexander. “Intramolecular direct arylation.” 2017. Doctoral Dissertation, University of Edinburgh. Accessed March 04, 2021. http://hdl.handle.net/1842/28820.

MLA Handbook (7th Edition):

Corrie, Thomas James Alexander. “Intramolecular direct arylation.” 2017. Web. 04 Mar 2021.

Vancouver:

Corrie TJA. Intramolecular direct arylation. [Internet] [Doctoral dissertation]. University of Edinburgh; 2017. [cited 2021 Mar 04]. Available from: http://hdl.handle.net/1842/28820.

Council of Science Editors:

Corrie TJA. Intramolecular direct arylation. [Doctoral Dissertation]. University of Edinburgh; 2017. Available from: http://hdl.handle.net/1842/28820


University of South Carolina

4. Key, Ryan J. Development of Nickel Catalyzed Cross-Coupling Methodologies.

Degree: PhD, Chemistry and Biochemistry, 2019, University of South Carolina

  In this work, we have addressed some of the issues surrounding catalytic crosscoupling reactions by using a nickel terpyridine catalyst, [Ni(tpy)(py)(CH3CN)2](PF6)2 in the Buchwald-Hartwig… (more)

Subjects/Keywords: Chemistry; nickel; cross-coupling; Atomic Layer Deposition; Suzuki reaction

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APA (6th Edition):

Key, R. J. (2019). Development of Nickel Catalyzed Cross-Coupling Methodologies. (Doctoral Dissertation). University of South Carolina. Retrieved from https://scholarcommons.sc.edu/etd/5324

Chicago Manual of Style (16th Edition):

Key, Ryan J. “Development of Nickel Catalyzed Cross-Coupling Methodologies.” 2019. Doctoral Dissertation, University of South Carolina. Accessed March 04, 2021. https://scholarcommons.sc.edu/etd/5324.

MLA Handbook (7th Edition):

Key, Ryan J. “Development of Nickel Catalyzed Cross-Coupling Methodologies.” 2019. Web. 04 Mar 2021.

Vancouver:

Key RJ. Development of Nickel Catalyzed Cross-Coupling Methodologies. [Internet] [Doctoral dissertation]. University of South Carolina; 2019. [cited 2021 Mar 04]. Available from: https://scholarcommons.sc.edu/etd/5324.

Council of Science Editors:

Key RJ. Development of Nickel Catalyzed Cross-Coupling Methodologies. [Doctoral Dissertation]. University of South Carolina; 2019. Available from: https://scholarcommons.sc.edu/etd/5324


Indian Institute of Science

5. Dhineshkumar, J. Iodine and Copper Catalyzed Oxidative Cross Coupling Reactions : Design and Development of Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions.

Degree: PhD, Faculty of Science, 2018, Indian Institute of Science

 Design and Development of Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions” is divided into two sections. Section-A, contains two chapters, describes the catalytic ability of iodine… (more)

Subjects/Keywords: Carbon-heteroatom Bond; Cross Dehydrogenative Coupling; Tetrabutylammonium Iodide; Cross-Hetero-Dehydrogenative Coupling Reaction; Phosphites; Quaternary Azides; Organic Chemistry

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APA (6th Edition):

Dhineshkumar, J. (2018). Iodine and Copper Catalyzed Oxidative Cross Coupling Reactions : Design and Development of Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions. (Doctoral Dissertation). Indian Institute of Science. Retrieved from http://etd.iisc.ac.in/handle/2005/3020

Chicago Manual of Style (16th Edition):

Dhineshkumar, J. “Iodine and Copper Catalyzed Oxidative Cross Coupling Reactions : Design and Development of Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions.” 2018. Doctoral Dissertation, Indian Institute of Science. Accessed March 04, 2021. http://etd.iisc.ac.in/handle/2005/3020.

MLA Handbook (7th Edition):

Dhineshkumar, J. “Iodine and Copper Catalyzed Oxidative Cross Coupling Reactions : Design and Development of Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions.” 2018. Web. 04 Mar 2021.

Vancouver:

Dhineshkumar J. Iodine and Copper Catalyzed Oxidative Cross Coupling Reactions : Design and Development of Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions. [Internet] [Doctoral dissertation]. Indian Institute of Science; 2018. [cited 2021 Mar 04]. Available from: http://etd.iisc.ac.in/handle/2005/3020.

Council of Science Editors:

Dhineshkumar J. Iodine and Copper Catalyzed Oxidative Cross Coupling Reactions : Design and Development of Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions. [Doctoral Dissertation]. Indian Institute of Science; 2018. Available from: http://etd.iisc.ac.in/handle/2005/3020


NSYSU

6. 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 March 04, 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. 04 Mar 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 Mar 04]. 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


University of Alberta

7. 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 March 04, 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. 04 Mar 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 Mar 04]. 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


University of KwaZulu-Natal

8. Molefe, Patience Snenhlanhla Sthembile. Base-Free Suzuki acylation reactions of sodium (aryl trihydroxyborate) salts: a novel synthesis of substituted aryl ketones.

Degree: 2018, University of KwaZulu-Natal

 Asymmetric biaryl ketones are important building block in organic chemistry since they occur in large number of biological active compounds, natural product, cosmetics as well… (more)

Subjects/Keywords: Base-free Suzuki.; Sodium salts.; Aryl trihydroxyborate.; Ketones.; Suzuki-Miyaura cross-coupling acylation reaction.

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APA (6th Edition):

Molefe, P. S. S. (2018). Base-Free Suzuki acylation reactions of sodium (aryl trihydroxyborate) salts: a novel synthesis of substituted aryl ketones. (Thesis). University of KwaZulu-Natal. Retrieved from https://researchspace.ukzn.ac.za/handle/10413/18146

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):

Molefe, Patience Snenhlanhla Sthembile. “Base-Free Suzuki acylation reactions of sodium (aryl trihydroxyborate) salts: a novel synthesis of substituted aryl ketones.” 2018. Thesis, University of KwaZulu-Natal. Accessed March 04, 2021. https://researchspace.ukzn.ac.za/handle/10413/18146.

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

MLA Handbook (7th Edition):

Molefe, Patience Snenhlanhla Sthembile. “Base-Free Suzuki acylation reactions of sodium (aryl trihydroxyborate) salts: a novel synthesis of substituted aryl ketones.” 2018. Web. 04 Mar 2021.

Vancouver:

Molefe PSS. Base-Free Suzuki acylation reactions of sodium (aryl trihydroxyborate) salts: a novel synthesis of substituted aryl ketones. [Internet] [Thesis]. University of KwaZulu-Natal; 2018. [cited 2021 Mar 04]. Available from: https://researchspace.ukzn.ac.za/handle/10413/18146.

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

Council of Science Editors:

Molefe PSS. Base-Free Suzuki acylation reactions of sodium (aryl trihydroxyborate) salts: a novel synthesis of substituted aryl ketones. [Thesis]. University of KwaZulu-Natal; 2018. Available from: https://researchspace.ukzn.ac.za/handle/10413/18146

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 March 04, 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. 04 Mar 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 Mar 04]. 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


Boston College

10. Zhang, Liang. Catalytic Conjunctive Cross-Coupling and Catalytic Diboration Reactions.

Degree: PhD, Chemistry, 2017, Boston College

 This dissertation will present four main projects focused on stereoselective construction of borylated compounds as well as their applications in asymmetric syntheses. The first two… (more)

Subjects/Keywords: boron-Wittig reaction; catalytic conjunctive cross-coupling; catalytic diboration; enantioselective synthesis; organoboronates

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APA (6th Edition):

Zhang, L. (2017). Catalytic Conjunctive Cross-Coupling and Catalytic Diboration Reactions. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:107561

Chicago Manual of Style (16th Edition):

Zhang, Liang. “Catalytic Conjunctive Cross-Coupling and Catalytic Diboration Reactions.” 2017. Doctoral Dissertation, Boston College. Accessed March 04, 2021. http://dlib.bc.edu/islandora/object/bc-ir:107561.

MLA Handbook (7th Edition):

Zhang, Liang. “Catalytic Conjunctive Cross-Coupling and Catalytic Diboration Reactions.” 2017. Web. 04 Mar 2021.

Vancouver:

Zhang L. Catalytic Conjunctive Cross-Coupling and Catalytic Diboration Reactions. [Internet] [Doctoral dissertation]. Boston College; 2017. [cited 2021 Mar 04]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:107561.

Council of Science Editors:

Zhang L. Catalytic Conjunctive Cross-Coupling and Catalytic Diboration Reactions. [Doctoral Dissertation]. Boston College; 2017. Available from: http://dlib.bc.edu/islandora/object/bc-ir:107561

11. D'Attoma, Joseph. Conception, synthèses et évaluations biologiques d’inhibiteurs à double cible : ALK et la restriction calorique : Design, synthesis and biological evaluations of inhibitors double target : ALK and caloric restriction.

Degree: Docteur es, Chimie, 2013, Université Claude Bernard – Lyon I

Les lymphomes à grandes cellules anaplasiques ou ALCL (Anaplastic Large-Cell Lymphoma) sont des cancers appartenant à la famille des lymphomes de type non-Hodgkin. La majorité… (more)

Subjects/Keywords: 2-acylaminothiazoles; Restriction calorique; ALCL; NPM-ALK; Réaction de Suzuki- Miyaura; Réaction de Buchwald-Hartwig; Réaction de Sonogashira; 2-acylaminothiazols; Caloric restriction; ALCL; NPM-ALK; Suzuki-Miyaura crosscoupling reaction; Buchwald-Hartwig cross-coupling reaction; Sonogashira cross-coupling reaction; 547

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APA (6th Edition):

D'Attoma, J. (2013). Conception, synthèses et évaluations biologiques d’inhibiteurs à double cible : ALK et la restriction calorique : Design, synthesis and biological evaluations of inhibitors double target : ALK and caloric restriction. (Doctoral Dissertation). Université Claude Bernard – Lyon I. Retrieved from http://www.theses.fr/2013LYO10243

Chicago Manual of Style (16th Edition):

D'Attoma, Joseph. “Conception, synthèses et évaluations biologiques d’inhibiteurs à double cible : ALK et la restriction calorique : Design, synthesis and biological evaluations of inhibitors double target : ALK and caloric restriction.” 2013. Doctoral Dissertation, Université Claude Bernard – Lyon I. Accessed March 04, 2021. http://www.theses.fr/2013LYO10243.

MLA Handbook (7th Edition):

D'Attoma, Joseph. “Conception, synthèses et évaluations biologiques d’inhibiteurs à double cible : ALK et la restriction calorique : Design, synthesis and biological evaluations of inhibitors double target : ALK and caloric restriction.” 2013. Web. 04 Mar 2021.

Vancouver:

D'Attoma J. Conception, synthèses et évaluations biologiques d’inhibiteurs à double cible : ALK et la restriction calorique : Design, synthesis and biological evaluations of inhibitors double target : ALK and caloric restriction. [Internet] [Doctoral dissertation]. Université Claude Bernard – Lyon I; 2013. [cited 2021 Mar 04]. Available from: http://www.theses.fr/2013LYO10243.

Council of Science Editors:

D'Attoma J. Conception, synthèses et évaluations biologiques d’inhibiteurs à double cible : ALK et la restriction calorique : Design, synthesis and biological evaluations of inhibitors double target : ALK and caloric restriction. [Doctoral Dissertation]. Université Claude Bernard – Lyon I; 2013. Available from: http://www.theses.fr/2013LYO10243


Kyoto University

12. Agata, Ryosuke. Development of Iron-Catalyzed Selective Cross-Coupling Reactions toward Natural Product Synthesis .

Degree: 2019, Kyoto University

Subjects/Keywords: Iron catalyst; Cross-coupling reaction; Natural product; Mechanistic study

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APA (6th Edition):

Agata, R. (2019). Development of Iron-Catalyzed Selective Cross-Coupling Reactions toward Natural Product Synthesis . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/242522

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):

Agata, Ryosuke. “Development of Iron-Catalyzed Selective Cross-Coupling Reactions toward Natural Product Synthesis .” 2019. Thesis, Kyoto University. Accessed March 04, 2021. http://hdl.handle.net/2433/242522.

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

MLA Handbook (7th Edition):

Agata, Ryosuke. “Development of Iron-Catalyzed Selective Cross-Coupling Reactions toward Natural Product Synthesis .” 2019. Web. 04 Mar 2021.

Vancouver:

Agata R. Development of Iron-Catalyzed Selective Cross-Coupling Reactions toward Natural Product Synthesis . [Internet] [Thesis]. Kyoto University; 2019. [cited 2021 Mar 04]. Available from: http://hdl.handle.net/2433/242522.

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

Council of Science Editors:

Agata R. Development of Iron-Catalyzed Selective Cross-Coupling Reactions toward Natural Product Synthesis . [Thesis]. Kyoto University; 2019. Available from: http://hdl.handle.net/2433/242522

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


Université Paris-Sud – Paris XI

13. 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 March 04, 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. 04 Mar 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 Mar 04]. 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


University of Gothenburg / Göteborgs Universitet

14. 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 (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 March 04, 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. 04 Mar 2021.

Vancouver:

Kleimark J. MECHANISTIC INVESTIGATIONS OF TRANSITION METAL CATALYZED REACTIONS. [Internet] [Thesis]. University of Gothenburg / Göteborgs Universitet; 2011. [cited 2021 Mar 04]. 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

15. Satou, Motoi. Synthesis of Ligands Bearing Poly(ethylene glycol) Chains and Their Application in Catalysis .

Degree: 2018, Kyoto University

Subjects/Keywords: Poly(ethylene glycol); Ligand Development; Transition Metal Catalyst; Oxidation Reaction; Cross-Coupling Reaction

Page 1 Page 2 Page 3 Page 4

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APA (6th Edition):

Satou, M. (2018). Synthesis of Ligands Bearing Poly(ethylene glycol) Chains and Their Application in Catalysis . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/232048

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):

Satou, Motoi. “Synthesis of Ligands Bearing Poly(ethylene glycol) Chains and Their Application in Catalysis .” 2018. Thesis, Kyoto University. Accessed March 04, 2021. http://hdl.handle.net/2433/232048.

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

MLA Handbook (7th Edition):

Satou, Motoi. “Synthesis of Ligands Bearing Poly(ethylene glycol) Chains and Their Application in Catalysis .” 2018. Web. 04 Mar 2021.

Vancouver:

Satou M. Synthesis of Ligands Bearing Poly(ethylene glycol) Chains and Their Application in Catalysis . [Internet] [Thesis]. Kyoto University; 2018. [cited 2021 Mar 04]. Available from: http://hdl.handle.net/2433/232048.

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

Council of Science Editors:

Satou M. Synthesis of Ligands Bearing Poly(ethylene glycol) Chains and Their Application in Catalysis . [Thesis]. Kyoto University; 2018. Available from: http://hdl.handle.net/2433/232048

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

16. Weeden, Jason. Organic and Organometallic Catalysts for Aqueous Nitrile Hydration and Carbon-Carbon Bond Forming Reactions.

Degree: 2013, University of Nevada – Reno

 This dissertation investigates the ability of the phosphine 1,3,5-triaza-7-phosphaadamantane (PTA) and derivatives to serve as either organocataysts or ancillary ligands coordinated to transition metal catalysts.… (more)

Subjects/Keywords: 1; 3; 5-triaza-7-phophaadamantane (PTA); Henry (Nitroaldol) Reaction; Morita-Baylis-Hillman Reaction; Nitrile Hydration; Ruthenium Arene Piano stool complexes; Suzuki Cross-Coupling

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APA (6th Edition):

Weeden, J. (2013). Organic and Organometallic Catalysts for Aqueous Nitrile Hydration and Carbon-Carbon Bond Forming Reactions. (Thesis). University of Nevada – Reno. Retrieved from http://hdl.handle.net/11714/3132

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):

Weeden, Jason. “Organic and Organometallic Catalysts for Aqueous Nitrile Hydration and Carbon-Carbon Bond Forming Reactions.” 2013. Thesis, University of Nevada – Reno. Accessed March 04, 2021. http://hdl.handle.net/11714/3132.

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

MLA Handbook (7th Edition):

Weeden, Jason. “Organic and Organometallic Catalysts for Aqueous Nitrile Hydration and Carbon-Carbon Bond Forming Reactions.” 2013. Web. 04 Mar 2021.

Vancouver:

Weeden J. Organic and Organometallic Catalysts for Aqueous Nitrile Hydration and Carbon-Carbon Bond Forming Reactions. [Internet] [Thesis]. University of Nevada – Reno; 2013. [cited 2021 Mar 04]. Available from: http://hdl.handle.net/11714/3132.

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

Council of Science Editors:

Weeden J. Organic and Organometallic Catalysts for Aqueous Nitrile Hydration and Carbon-Carbon Bond Forming Reactions. [Thesis]. University of Nevada – Reno; 2013. Available from: http://hdl.handle.net/11714/3132

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


University of South Africa

17. Paumo, Hugues Kamdem. 2-Aryl-6,8-Dibromo-4-Chloroquinazoline as scaffold for the synthesis of Novel 2,6,8-Triaryl-4-(Phenylethynyl)Quinazolines with potential photophysical properties .

Degree: 2014, University of South Africa

 The 2-aryl-6,8-dibromoquinazolin-4(3H)-ones were prepared in a single-pot operation by condensing 6,8-dibromoanthranilamide and aryl aldehydes in the presence of molecular iodine in ethanol. Treatment of the… (more)

Subjects/Keywords: 2-aryl-6,8-dibromoquinazolin-4(3H)-ones; 2-aryl-4-chloro-6; 8-dibromoquinazolines; 2-aryl-6,8-dibromo-4-(phenylethynyl)quinazolines; 2,6,8-triaryl-4-(phenylethynyl)quinazolines; Sonogashira cross-coupling reaction; Suzuki-Miyaura cross-coupling reaction; Absorption and emission properties

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APA (6th Edition):

Paumo, H. K. (2014). 2-Aryl-6,8-Dibromo-4-Chloroquinazoline as scaffold for the synthesis of Novel 2,6,8-Triaryl-4-(Phenylethynyl)Quinazolines with potential photophysical properties . (Masters Thesis). University of South Africa. Retrieved from http://hdl.handle.net/10500/14197

Chicago Manual of Style (16th Edition):

Paumo, Hugues Kamdem. “2-Aryl-6,8-Dibromo-4-Chloroquinazoline as scaffold for the synthesis of Novel 2,6,8-Triaryl-4-(Phenylethynyl)Quinazolines with potential photophysical properties .” 2014. Masters Thesis, University of South Africa. Accessed March 04, 2021. http://hdl.handle.net/10500/14197.

MLA Handbook (7th Edition):

Paumo, Hugues Kamdem. “2-Aryl-6,8-Dibromo-4-Chloroquinazoline as scaffold for the synthesis of Novel 2,6,8-Triaryl-4-(Phenylethynyl)Quinazolines with potential photophysical properties .” 2014. Web. 04 Mar 2021.

Vancouver:

Paumo HK. 2-Aryl-6,8-Dibromo-4-Chloroquinazoline as scaffold for the synthesis of Novel 2,6,8-Triaryl-4-(Phenylethynyl)Quinazolines with potential photophysical properties . [Internet] [Masters thesis]. University of South Africa; 2014. [cited 2021 Mar 04]. Available from: http://hdl.handle.net/10500/14197.

Council of Science Editors:

Paumo HK. 2-Aryl-6,8-Dibromo-4-Chloroquinazoline as scaffold for the synthesis of Novel 2,6,8-Triaryl-4-(Phenylethynyl)Quinazolines with potential photophysical properties . [Masters Thesis]. University of South Africa; 2014. Available from: http://hdl.handle.net/10500/14197


University of South Africa

18. Makelane, Hlamulo Reply. Regioselectivity of palladium-catalyzed sonogashira cross-coupling of 2-aryl-4-chloro-3-iodoquinoline- derivatives with terminal alkynes .

Degree: 2010, University of South Africa

 Sonogashira cross-coupling of 2-aryl-4-chloro-3-iodoquinoline derivatives with stoichiometric amount of terminal alkynes in the presence of bis(triphenylphosphine)palladium(II)chloride and copper iodide in triethylamine afforded the 3-(alkynyl)-2-aryl-4-chloroquinoline, exclusively.… (more)

Subjects/Keywords: 2-aryl-4-chloro-3-iodoquinoline; Sonogashira cross-coupling reaction; Suzuki cross-coupling reaction

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APA (6th Edition):

Makelane, H. R. (2010). Regioselectivity of palladium-catalyzed sonogashira cross-coupling of 2-aryl-4-chloro-3-iodoquinoline- derivatives with terminal alkynes . (Masters Thesis). University of South Africa. Retrieved from http://hdl.handle.net/10500/3838

Chicago Manual of Style (16th Edition):

Makelane, Hlamulo Reply. “Regioselectivity of palladium-catalyzed sonogashira cross-coupling of 2-aryl-4-chloro-3-iodoquinoline- derivatives with terminal alkynes .” 2010. Masters Thesis, University of South Africa. Accessed March 04, 2021. http://hdl.handle.net/10500/3838.

MLA Handbook (7th Edition):

Makelane, Hlamulo Reply. “Regioselectivity of palladium-catalyzed sonogashira cross-coupling of 2-aryl-4-chloro-3-iodoquinoline- derivatives with terminal alkynes .” 2010. Web. 04 Mar 2021.

Vancouver:

Makelane HR. Regioselectivity of palladium-catalyzed sonogashira cross-coupling of 2-aryl-4-chloro-3-iodoquinoline- derivatives with terminal alkynes . [Internet] [Masters thesis]. University of South Africa; 2010. [cited 2021 Mar 04]. Available from: http://hdl.handle.net/10500/3838.

Council of Science Editors:

Makelane HR. Regioselectivity of palladium-catalyzed sonogashira cross-coupling of 2-aryl-4-chloro-3-iodoquinoline- derivatives with terminal alkynes . [Masters Thesis]. University of South Africa; 2010. Available from: http://hdl.handle.net/10500/3838


Kyoto University / 京都大学

19. Haraguchi, Ryosuke. Studies on Preparation of Functionalized Organozinc Reagents via Zinciomethylation : 亜鉛メチル化による官能基化された有機亜鉛反応剤の調製に関する研究.

Degree: 博士(工学), 2016, Kyoto University / 京都大学

新制・課程博士

甲第19726号

工博第4181号

Subjects/Keywords: Bis(iodozincio)methane; Organozinc reagent; Cross-coupling reaction; Asymmetric synthesis; Carbocycle

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APA (6th Edition):

Haraguchi, R. (2016). Studies on Preparation of Functionalized Organozinc Reagents via Zinciomethylation : 亜鉛メチル化による官能基化された有機亜鉛反応剤の調製に関する研究. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/215552 ; http://dx.doi.org/10.14989/doctor.k19726

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):

Haraguchi, Ryosuke. “Studies on Preparation of Functionalized Organozinc Reagents via Zinciomethylation : 亜鉛メチル化による官能基化された有機亜鉛反応剤の調製に関する研究.” 2016. Thesis, Kyoto University / 京都大学. Accessed March 04, 2021. http://hdl.handle.net/2433/215552 ; http://dx.doi.org/10.14989/doctor.k19726.

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

MLA Handbook (7th Edition):

Haraguchi, Ryosuke. “Studies on Preparation of Functionalized Organozinc Reagents via Zinciomethylation : 亜鉛メチル化による官能基化された有機亜鉛反応剤の調製に関する研究.” 2016. Web. 04 Mar 2021.

Vancouver:

Haraguchi R. Studies on Preparation of Functionalized Organozinc Reagents via Zinciomethylation : 亜鉛メチル化による官能基化された有機亜鉛反応剤の調製に関する研究. [Internet] [Thesis]. Kyoto University / 京都大学; 2016. [cited 2021 Mar 04]. Available from: http://hdl.handle.net/2433/215552 ; http://dx.doi.org/10.14989/doctor.k19726.

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

Council of Science Editors:

Haraguchi R. Studies on Preparation of Functionalized Organozinc Reagents via Zinciomethylation : 亜鉛メチル化による官能基化された有機亜鉛反応剤の調製に関する研究. [Thesis]. Kyoto University / 京都大学; 2016. Available from: http://hdl.handle.net/2433/215552 ; http://dx.doi.org/10.14989/doctor.k19726

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

20. 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 March 04, 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. 04 Mar 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 Mar 04]. 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


Indian Institute of Science

21. Yogesh, S. Design and Development of Metal-free Cross Dehydrogenative Coupling Reactions for the Construction of C-S, C-O and C-C bonds.

Degree: PhD, Faculty of Science, 2018, Indian Institute of Science

 The thesis entitled “Design and Development of Metal-Free Cross Dehydrogenative Coupling Reactions for the construction of C-S, C-O and C-C bonds” is divided into three… (more)

Subjects/Keywords: Cross Dehydrogenative Coupling Reactions; Chemoselective α-Aminoxylation; Acylation Quinolines; Transition Metal Free Minisci Reaction; CDC Reactions; Dimethyl Sulfoxide; Carbonyl Compounds; Ketones; Pyrazolones; Orcanic Chemistry

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APA (6th Edition):

Yogesh, S. (2018). Design and Development of Metal-free Cross Dehydrogenative Coupling Reactions for the Construction of C-S, C-O and C-C bonds. (Doctoral Dissertation). Indian Institute of Science. Retrieved from http://etd.iisc.ac.in/handle/2005/3698

Chicago Manual of Style (16th Edition):

Yogesh, S. “Design and Development of Metal-free Cross Dehydrogenative Coupling Reactions for the Construction of C-S, C-O and C-C bonds.” 2018. Doctoral Dissertation, Indian Institute of Science. Accessed March 04, 2021. http://etd.iisc.ac.in/handle/2005/3698.

MLA Handbook (7th Edition):

Yogesh, S. “Design and Development of Metal-free Cross Dehydrogenative Coupling Reactions for the Construction of C-S, C-O and C-C bonds.” 2018. Web. 04 Mar 2021.

Vancouver:

Yogesh S. Design and Development of Metal-free Cross Dehydrogenative Coupling Reactions for the Construction of C-S, C-O and C-C bonds. [Internet] [Doctoral dissertation]. Indian Institute of Science; 2018. [cited 2021 Mar 04]. Available from: http://etd.iisc.ac.in/handle/2005/3698.

Council of Science Editors:

Yogesh S. Design and Development of Metal-free Cross Dehydrogenative Coupling Reactions for the Construction of C-S, C-O and C-C bonds. [Doctoral Dissertation]. Indian Institute of Science; 2018. Available from: http://etd.iisc.ac.in/handle/2005/3698

22. 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 (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 March 04, 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. 04 Mar 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 Mar 04]. 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


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 (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 March 04, 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. 04 Mar 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 Mar 04]. 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

24. XUE FEI. NICKEL-CATALYZED CARBON-CARBON BOND FORMATION REACTIONS.

Degree: 2015, National University of Singapore

Subjects/Keywords: Nickel catalyst; carbon-carbon formation; cross-coupling; arylmagnesiation; domino reaction; cyclotrimerizatio

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APA (6th Edition):

FEI, X. (2015). NICKEL-CATALYZED CARBON-CARBON BOND FORMATION REACTIONS. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/122709

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):

FEI, XUE. “NICKEL-CATALYZED CARBON-CARBON BOND FORMATION REACTIONS.” 2015. Thesis, National University of Singapore. Accessed March 04, 2021. http://scholarbank.nus.edu.sg/handle/10635/122709.

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

MLA Handbook (7th Edition):

FEI, XUE. “NICKEL-CATALYZED CARBON-CARBON BOND FORMATION REACTIONS.” 2015. Web. 04 Mar 2021.

Vancouver:

FEI X. NICKEL-CATALYZED CARBON-CARBON BOND FORMATION REACTIONS. [Internet] [Thesis]. National University of Singapore; 2015. [cited 2021 Mar 04]. Available from: http://scholarbank.nus.edu.sg/handle/10635/122709.

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

Council of Science Editors:

FEI X. NICKEL-CATALYZED CARBON-CARBON BOND FORMATION REACTIONS. [Thesis]. National University of Singapore; 2015. Available from: http://scholarbank.nus.edu.sg/handle/10635/122709

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


University of Toronto

25. Rosocha, Yaroslav Gregory S. Development and Investigation of Electrocyclization Reactions Leading Towards Indene and Thiatriazole Formation and their Functionalization.

Degree: 2011, University of Toronto

PhD Advisors/Committee Members: Batey, Robert A., Chemistry.

Subjects/Keywords: Indene, Thiatriazole, Thiotetrazole, Electrocyclization, Cascade reaction, Isoquinoline, Cross-coupling, HIV inhibitor; 0490

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APA (6th Edition):

Rosocha, Y. G. S. (2011). Development and Investigation of Electrocyclization Reactions Leading Towards Indene and Thiatriazole Formation and their Functionalization. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/32082

Chicago Manual of Style (16th Edition):

Rosocha, Yaroslav Gregory S. “Development and Investigation of Electrocyclization Reactions Leading Towards Indene and Thiatriazole Formation and their Functionalization.” 2011. Doctoral Dissertation, University of Toronto. Accessed March 04, 2021. http://hdl.handle.net/1807/32082.

MLA Handbook (7th Edition):

Rosocha, Yaroslav Gregory S. “Development and Investigation of Electrocyclization Reactions Leading Towards Indene and Thiatriazole Formation and their Functionalization.” 2011. Web. 04 Mar 2021.

Vancouver:

Rosocha YGS. Development and Investigation of Electrocyclization Reactions Leading Towards Indene and Thiatriazole Formation and their Functionalization. [Internet] [Doctoral dissertation]. University of Toronto; 2011. [cited 2021 Mar 04]. Available from: http://hdl.handle.net/1807/32082.

Council of Science Editors:

Rosocha YGS. Development and Investigation of Electrocyclization Reactions Leading Towards Indene and Thiatriazole Formation and their Functionalization. [Doctoral Dissertation]. University of Toronto; 2011. Available from: http://hdl.handle.net/1807/32082


Laurentian University

26. Landry, Eric D. Star-structured polyethylene nanoparticles via Pd-catalyzed living polymerization : synthesis, characterization, and catalytic applications.

Degree: 2015, Laurentian University

 The arm-first synthesis of large unimolecular star-structured polyethylene nanoparticles or SPE-NPs (MW > 1,000 kg/mol, PDI ≈ 1.1) joined by a cross-linked polynorbornadiene (PNBD) core… (more)

Subjects/Keywords: star-structured polyethylene nanoparticles; cross-linked polynorbornadiene (PNBD); SPE-NPs; living ethylene polymerization; hydrogenation reactions of terminal alkenes and alkynes; Heck coupling reaction; iodobenzene; n-butyl acrylate

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APA (6th Edition):

Landry, E. D. (2015). Star-structured polyethylene nanoparticles via Pd-catalyzed living polymerization : synthesis, characterization, and catalytic applications. (Thesis). Laurentian University. Retrieved from https://zone.biblio.laurentian.ca/dspace/handle/10219/2420

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):

Landry, Eric D. “Star-structured polyethylene nanoparticles via Pd-catalyzed living polymerization : synthesis, characterization, and catalytic applications. ” 2015. Thesis, Laurentian University. Accessed March 04, 2021. https://zone.biblio.laurentian.ca/dspace/handle/10219/2420.

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

MLA Handbook (7th Edition):

Landry, Eric D. “Star-structured polyethylene nanoparticles via Pd-catalyzed living polymerization : synthesis, characterization, and catalytic applications. ” 2015. Web. 04 Mar 2021.

Vancouver:

Landry ED. Star-structured polyethylene nanoparticles via Pd-catalyzed living polymerization : synthesis, characterization, and catalytic applications. [Internet] [Thesis]. Laurentian University; 2015. [cited 2021 Mar 04]. Available from: https://zone.biblio.laurentian.ca/dspace/handle/10219/2420.

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

Council of Science Editors:

Landry ED. Star-structured polyethylene nanoparticles via Pd-catalyzed living polymerization : synthesis, characterization, and catalytic applications. [Thesis]. Laurentian University; 2015. Available from: https://zone.biblio.laurentian.ca/dspace/handle/10219/2420

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

27. Haraguchi, Ryosuke. Studies on Preparation of Functionalized Organozinc Reagents via Zinciomethylation .

Degree: 2016, Kyoto University

Subjects/Keywords: Bis(iodozincio)methane; Organozinc reagent; Cross-coupling reaction; Asymmetric synthesis; Carbocycle

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APA (6th Edition):

Haraguchi, R. (2016). Studies on Preparation of Functionalized Organozinc Reagents via Zinciomethylation . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/215552

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):

Haraguchi, Ryosuke. “Studies on Preparation of Functionalized Organozinc Reagents via Zinciomethylation .” 2016. Thesis, Kyoto University. Accessed March 04, 2021. http://hdl.handle.net/2433/215552.

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

MLA Handbook (7th Edition):

Haraguchi, Ryosuke. “Studies on Preparation of Functionalized Organozinc Reagents via Zinciomethylation .” 2016. Web. 04 Mar 2021.

Vancouver:

Haraguchi R. Studies on Preparation of Functionalized Organozinc Reagents via Zinciomethylation . [Internet] [Thesis]. Kyoto University; 2016. [cited 2021 Mar 04]. Available from: http://hdl.handle.net/2433/215552.

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

Council of Science Editors:

Haraguchi R. Studies on Preparation of Functionalized Organozinc Reagents via Zinciomethylation . [Thesis]. Kyoto University; 2016. Available from: http://hdl.handle.net/2433/215552

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

28. 山田,重之. Studies on the Developments of Selective Synthetic Methods for Polyfluoroalkene Derivatives by Employing Organometallic Reagents.

Degree: Kyoto Institute of Technology / 京都工芸繊維大学

This thesis consists of five chapters. Chapter 1 describes general introduction including description of fluorinated alkenes as well as brief summary of the results that… (more)

Subjects/Keywords: Organofluorine Compounds; Fluorinated Alkenes; Organometallic Reagents; Addition-elimination Reaction; Fluorine-metal Exchange Reaction; Cross-coupling Reaction

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APA (6th Edition):

山田,重之. (n.d.). Studies on the Developments of Selective Synthetic Methods for Polyfluoroalkene Derivatives by Employing Organometallic Reagents. (Thesis). Kyoto Institute of Technology / 京都工芸繊維大学. Retrieved from http://hdl.handle.net/10212/1612

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

山田,重之. “Studies on the Developments of Selective Synthetic Methods for Polyfluoroalkene Derivatives by Employing Organometallic Reagents.” Thesis, Kyoto Institute of Technology / 京都工芸繊維大学. Accessed March 04, 2021. http://hdl.handle.net/10212/1612.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

山田,重之. “Studies on the Developments of Selective Synthetic Methods for Polyfluoroalkene Derivatives by Employing Organometallic Reagents.” Web. 04 Mar 2021.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
No year of publication.

Vancouver:

山田,重之. Studies on the Developments of Selective Synthetic Methods for Polyfluoroalkene Derivatives by Employing Organometallic Reagents. [Internet] [Thesis]. Kyoto Institute of Technology / 京都工芸繊維大学; [cited 2021 Mar 04]. Available from: http://hdl.handle.net/10212/1612.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

山田,重之. Studies on the Developments of Selective Synthetic Methods for Polyfluoroalkene Derivatives by Employing Organometallic Reagents. [Thesis]. Kyoto Institute of Technology / 京都工芸繊維大学; Available from: http://hdl.handle.net/10212/1612

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

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 March 04, 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. 04 Mar 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 Mar 04]. 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

30. Nakajima, Sho. Mechanistic and Synthetic Studies on Iron-Bisphosphine-Catalyzed Cross-Coupling Reactions of Alkyl Halides : ハロゲン化アルキルを用いる鉄触媒クロスカップリング反応の機構および開発に関する研究.

Degree: 博士(工学), 2017, Kyoto University / 京都大学

新制・課程博士

甲第20391号

工博第4328号

Subjects/Keywords: Iron catalyst; Cross-coupling reaction; Alkyl halide; X-ray absorption spectroscopy; Mechanistic study; Bisphosphine ligand

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APA (6th Edition):

Nakajima, S. (2017). Mechanistic and Synthetic Studies on Iron-Bisphosphine-Catalyzed Cross-Coupling Reactions of Alkyl Halides : ハロゲン化アルキルを用いる鉄触媒クロスカップリング反応の機構および開発に関する研究. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/225616 ; http://dx.doi.org/10.14989/doctor.k20391

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):

Nakajima, Sho. “Mechanistic and Synthetic Studies on Iron-Bisphosphine-Catalyzed Cross-Coupling Reactions of Alkyl Halides : ハロゲン化アルキルを用いる鉄触媒クロスカップリング反応の機構および開発に関する研究.” 2017. Thesis, Kyoto University / 京都大学. Accessed March 04, 2021. http://hdl.handle.net/2433/225616 ; http://dx.doi.org/10.14989/doctor.k20391.

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

MLA Handbook (7th Edition):

Nakajima, Sho. “Mechanistic and Synthetic Studies on Iron-Bisphosphine-Catalyzed Cross-Coupling Reactions of Alkyl Halides : ハロゲン化アルキルを用いる鉄触媒クロスカップリング反応の機構および開発に関する研究.” 2017. Web. 04 Mar 2021.

Vancouver:

Nakajima S. Mechanistic and Synthetic Studies on Iron-Bisphosphine-Catalyzed Cross-Coupling Reactions of Alkyl Halides : ハロゲン化アルキルを用いる鉄触媒クロスカップリング反応の機構および開発に関する研究. [Internet] [Thesis]. Kyoto University / 京都大学; 2017. [cited 2021 Mar 04]. Available from: http://hdl.handle.net/2433/225616 ; http://dx.doi.org/10.14989/doctor.k20391.

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

Council of Science Editors:

Nakajima S. Mechanistic and Synthetic Studies on Iron-Bisphosphine-Catalyzed Cross-Coupling Reactions of Alkyl Halides : ハロゲン化アルキルを用いる鉄触媒クロスカップリング反応の機構および開発に関する研究. [Thesis]. Kyoto University / 京都大学; 2017. Available from: http://hdl.handle.net/2433/225616 ; http://dx.doi.org/10.14989/doctor.k20391

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

[1] [2]

.