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You searched for subject:( Hydroboration). Showing records 1 – 30 of 47 total matches.

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Boston College

1. Ely, Robert John. Regio- and stereoselective Ni-catalyzed 1,4-hydroboration and diboration of 1,3-dienes: Access to stereodefined (Z)-allyboron reagents and application towards the total synthesis of discodermolide.

Degree: PhD, Chemistry, 2012, Boston College

 Detailed within this dissertation are the developments of novel hydroboration and diboration methodologies to access allylboron reagents and efforts towards the application of these methods… (more)

Subjects/Keywords: Discodermolide; Hydroboration; Diboration

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APA (6th Edition):

Ely, R. J. (2012). Regio- and stereoselective Ni-catalyzed 1,4-hydroboration and diboration of 1,3-dienes: Access to stereodefined (Z)-allyboron reagents and application towards the total synthesis of discodermolide. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:104383

Chicago Manual of Style (16th Edition):

Ely, Robert John. “Regio- and stereoselective Ni-catalyzed 1,4-hydroboration and diboration of 1,3-dienes: Access to stereodefined (Z)-allyboron reagents and application towards the total synthesis of discodermolide.” 2012. Doctoral Dissertation, Boston College. Accessed October 22, 2019. http://dlib.bc.edu/islandora/object/bc-ir:104383.

MLA Handbook (7th Edition):

Ely, Robert John. “Regio- and stereoselective Ni-catalyzed 1,4-hydroboration and diboration of 1,3-dienes: Access to stereodefined (Z)-allyboron reagents and application towards the total synthesis of discodermolide.” 2012. Web. 22 Oct 2019.

Vancouver:

Ely RJ. Regio- and stereoselective Ni-catalyzed 1,4-hydroboration and diboration of 1,3-dienes: Access to stereodefined (Z)-allyboron reagents and application towards the total synthesis of discodermolide. [Internet] [Doctoral dissertation]. Boston College; 2012. [cited 2019 Oct 22]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:104383.

Council of Science Editors:

Ely RJ. Regio- and stereoselective Ni-catalyzed 1,4-hydroboration and diboration of 1,3-dienes: Access to stereodefined (Z)-allyboron reagents and application towards the total synthesis of discodermolide. [Doctoral Dissertation]. Boston College; 2012. Available from: http://dlib.bc.edu/islandora/object/bc-ir:104383


University of KwaZulu-Natal

2. [No author]. Thermal transformation of organoboranes : applicability of ¹¹B NMR spectroscopy and supporting molecular modelling.

Degree: Chemistry, 2008, University of KwaZulu-Natal

 The high temperature transformations of trialkylboranes were investigated in the range: 50- 200 ºC. The extent of dealkylation was found to be linked to temperature… (more)

Subjects/Keywords: Chemistry.; Hydroboration.; Organoboron compounds.

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APA (6th Edition):

author], [. (2008). Thermal transformation of organoboranes : applicability of ¹¹B NMR spectroscopy and supporting molecular modelling. (Thesis). University of KwaZulu-Natal. Retrieved from http://hdl.handle.net/10413/946

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):

author], [No. “Thermal transformation of organoboranes : applicability of ¹¹B NMR spectroscopy and supporting molecular modelling. ” 2008. Thesis, University of KwaZulu-Natal. Accessed October 22, 2019. http://hdl.handle.net/10413/946.

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

MLA Handbook (7th Edition):

author], [No. “Thermal transformation of organoboranes : applicability of ¹¹B NMR spectroscopy and supporting molecular modelling. ” 2008. Web. 22 Oct 2019.

Vancouver:

author] [. Thermal transformation of organoboranes : applicability of ¹¹B NMR spectroscopy and supporting molecular modelling. [Internet] [Thesis]. University of KwaZulu-Natal; 2008. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/10413/946.

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

Council of Science Editors:

author] [. Thermal transformation of organoboranes : applicability of ¹¹B NMR spectroscopy and supporting molecular modelling. [Thesis]. University of KwaZulu-Natal; 2008. Available from: http://hdl.handle.net/10413/946

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


Queens University

3. Bailey, Adrian. Borenium Cations as Catalysts for the Reduction of Organic Molecules and Mechanistic Investigations into their Mode of Operation .

Degree: Chemistry, 2012, Queens University

 The generation and isolation of two novel borenium cations has been described. The observation that the reaction of the Lewis acid B(C6F5)3 and the Lewis… (more)

Subjects/Keywords: Reduction; Hydroboration; Boron cations; Catalysis

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APA (6th Edition):

Bailey, A. (2012). Borenium Cations as Catalysts for the Reduction of Organic Molecules and Mechanistic Investigations into their Mode of Operation . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/7593

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, Adrian. “Borenium Cations as Catalysts for the Reduction of Organic Molecules and Mechanistic Investigations into their Mode of Operation .” 2012. Thesis, Queens University. Accessed October 22, 2019. http://hdl.handle.net/1974/7593.

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

MLA Handbook (7th Edition):

Bailey, Adrian. “Borenium Cations as Catalysts for the Reduction of Organic Molecules and Mechanistic Investigations into their Mode of Operation .” 2012. Web. 22 Oct 2019.

Vancouver:

Bailey A. Borenium Cations as Catalysts for the Reduction of Organic Molecules and Mechanistic Investigations into their Mode of Operation . [Internet] [Thesis]. Queens University; 2012. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1974/7593.

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

Council of Science Editors:

Bailey A. Borenium Cations as Catalysts for the Reduction of Organic Molecules and Mechanistic Investigations into their Mode of Operation . [Thesis]. Queens University; 2012. Available from: http://hdl.handle.net/1974/7593

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


Queens University

4. Lata, Christopher. Cationic Rhodium-Catalyzed Hydroboration: Investigations into Electronic and Ligand Effects; Lewis-Acid Reaction Acceleration and Regioselectivity Change .

Degree: Chemistry, 2009, Queens University

 Mechanistic aspects of the asymmetric rhodium catalyzed hydroboration of vinyl arenes with catecholborane (HBCat) and pinacolborane (HBPin) have been probed. Competition studies conducted with catalysts… (more)

Subjects/Keywords: Chemistry; Hydroboration

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APA (6th Edition):

Lata, C. (2009). Cationic Rhodium-Catalyzed Hydroboration: Investigations into Electronic and Ligand Effects; Lewis-Acid Reaction Acceleration and Regioselectivity Change . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/5283

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):

Lata, Christopher. “Cationic Rhodium-Catalyzed Hydroboration: Investigations into Electronic and Ligand Effects; Lewis-Acid Reaction Acceleration and Regioselectivity Change .” 2009. Thesis, Queens University. Accessed October 22, 2019. http://hdl.handle.net/1974/5283.

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

MLA Handbook (7th Edition):

Lata, Christopher. “Cationic Rhodium-Catalyzed Hydroboration: Investigations into Electronic and Ligand Effects; Lewis-Acid Reaction Acceleration and Regioselectivity Change .” 2009. Web. 22 Oct 2019.

Vancouver:

Lata C. Cationic Rhodium-Catalyzed Hydroboration: Investigations into Electronic and Ligand Effects; Lewis-Acid Reaction Acceleration and Regioselectivity Change . [Internet] [Thesis]. Queens University; 2009. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1974/5283.

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

Council of Science Editors:

Lata C. Cationic Rhodium-Catalyzed Hydroboration: Investigations into Electronic and Ligand Effects; Lewis-Acid Reaction Acceleration and Regioselectivity Change . [Thesis]. Queens University; 2009. Available from: http://hdl.handle.net/1974/5283

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


University of Edinburgh

5. Carney, Jonathan Robert. Manganese-catalysed hydrofunctionalisation of alkenes.

Degree: PhD, 2019, University of Edinburgh

 The development of new first-row transition metal catalysts as both replacements for precious metals catalysts and in the search for novel reactivity is a crucial… (more)

Subjects/Keywords: manganese; catalysis; hydrosilylation; hydroboration

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APA (6th Edition):

Carney, J. R. (2019). Manganese-catalysed hydrofunctionalisation of alkenes. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/35699

Chicago Manual of Style (16th Edition):

Carney, Jonathan Robert. “Manganese-catalysed hydrofunctionalisation of alkenes.” 2019. Doctoral Dissertation, University of Edinburgh. Accessed October 22, 2019. http://hdl.handle.net/1842/35699.

MLA Handbook (7th Edition):

Carney, Jonathan Robert. “Manganese-catalysed hydrofunctionalisation of alkenes.” 2019. Web. 22 Oct 2019.

Vancouver:

Carney JR. Manganese-catalysed hydrofunctionalisation of alkenes. [Internet] [Doctoral dissertation]. University of Edinburgh; 2019. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1842/35699.

Council of Science Editors:

Carney JR. Manganese-catalysed hydrofunctionalisation of alkenes. [Doctoral Dissertation]. University of Edinburgh; 2019. Available from: http://hdl.handle.net/1842/35699


Rochester Institute of Technology

6. Feng, Pingyun. Hydroboration-oxidation of styrene, 2,3 dihydrofuran and quadricyclene dimethylester promoted by Wilkinson's catalyst.

Degree: School of Chemistry and Materials Science (COS), 1991, Rochester Institute of Technology

None provided. Advisors/Committee Members: Morrill, Terence.

Subjects/Keywords: Furans; Hydroboration; Styrene

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APA (6th Edition):

Feng, P. (1991). Hydroboration-oxidation of styrene, 2,3 dihydrofuran and quadricyclene dimethylester promoted by Wilkinson's catalyst. (Thesis). Rochester Institute of Technology. Retrieved from https://scholarworks.rit.edu/theses/5983

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):

Feng, Pingyun. “Hydroboration-oxidation of styrene, 2,3 dihydrofuran and quadricyclene dimethylester promoted by Wilkinson's catalyst.” 1991. Thesis, Rochester Institute of Technology. Accessed October 22, 2019. https://scholarworks.rit.edu/theses/5983.

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

MLA Handbook (7th Edition):

Feng, Pingyun. “Hydroboration-oxidation of styrene, 2,3 dihydrofuran and quadricyclene dimethylester promoted by Wilkinson's catalyst.” 1991. Web. 22 Oct 2019.

Vancouver:

Feng P. Hydroboration-oxidation of styrene, 2,3 dihydrofuran and quadricyclene dimethylester promoted by Wilkinson's catalyst. [Internet] [Thesis]. Rochester Institute of Technology; 1991. [cited 2019 Oct 22]. Available from: https://scholarworks.rit.edu/theses/5983.

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

Council of Science Editors:

Feng P. Hydroboration-oxidation of styrene, 2,3 dihydrofuran and quadricyclene dimethylester promoted by Wilkinson's catalyst. [Thesis]. Rochester Institute of Technology; 1991. Available from: https://scholarworks.rit.edu/theses/5983

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


Rochester Institute of Technology

7. Lu, Qingyi. Halogenolyses of tri-alkylborane.

Degree: School of Chemistry and Materials Science (COS), 1990, Rochester Institute of Technology

None provided. Advisors/Committee Members: Lakaen, Gerard.

Subjects/Keywords: Hydroboration; Organohalogen compounds

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APA (6th Edition):

Lu, Q. (1990). Halogenolyses of tri-alkylborane. (Thesis). Rochester Institute of Technology. Retrieved from https://scholarworks.rit.edu/theses/5961

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):

Lu, Qingyi. “Halogenolyses of tri-alkylborane.” 1990. Thesis, Rochester Institute of Technology. Accessed October 22, 2019. https://scholarworks.rit.edu/theses/5961.

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

MLA Handbook (7th Edition):

Lu, Qingyi. “Halogenolyses of tri-alkylborane.” 1990. Web. 22 Oct 2019.

Vancouver:

Lu Q. Halogenolyses of tri-alkylborane. [Internet] [Thesis]. Rochester Institute of Technology; 1990. [cited 2019 Oct 22]. Available from: https://scholarworks.rit.edu/theses/5961.

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

Council of Science Editors:

Lu Q. Halogenolyses of tri-alkylborane. [Thesis]. Rochester Institute of Technology; 1990. Available from: https://scholarworks.rit.edu/theses/5961

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


Princeton University

8. Obligacion, Jennifer Victoriano. BASE METAL CATALYSIS FOR THE SYNTHESIS OF ORGANOBORON COMPOUNDS .

Degree: PhD, 2017, Princeton University

 The versatility of organoboron compounds in organic synthesis inspires the discovery of efficient and sustainable methods for their synthesis; hence, providing more inexpensive, less toxic,… (more)

Subjects/Keywords: C-H Borylation; Cobalt catalysis; Hydroboration

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APA (6th Edition):

Obligacion, J. V. (2017). BASE METAL CATALYSIS FOR THE SYNTHESIS OF ORGANOBORON COMPOUNDS . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp014m90dz102

Chicago Manual of Style (16th Edition):

Obligacion, Jennifer Victoriano. “BASE METAL CATALYSIS FOR THE SYNTHESIS OF ORGANOBORON COMPOUNDS .” 2017. Doctoral Dissertation, Princeton University. Accessed October 22, 2019. http://arks.princeton.edu/ark:/88435/dsp014m90dz102.

MLA Handbook (7th Edition):

Obligacion, Jennifer Victoriano. “BASE METAL CATALYSIS FOR THE SYNTHESIS OF ORGANOBORON COMPOUNDS .” 2017. Web. 22 Oct 2019.

Vancouver:

Obligacion JV. BASE METAL CATALYSIS FOR THE SYNTHESIS OF ORGANOBORON COMPOUNDS . [Internet] [Doctoral dissertation]. Princeton University; 2017. [cited 2019 Oct 22]. Available from: http://arks.princeton.edu/ark:/88435/dsp014m90dz102.

Council of Science Editors:

Obligacion JV. BASE METAL CATALYSIS FOR THE SYNTHESIS OF ORGANOBORON COMPOUNDS . [Doctoral Dissertation]. Princeton University; 2017. Available from: http://arks.princeton.edu/ark:/88435/dsp014m90dz102


Université Paris-Sud – Paris XI

9. Blondiaux, Enguerrand. Recyclage du CO2 : Une alternative à la pétrochimie pour la synthèse de molécules azotées : CO2 recycling : An alternative to petrochemistry for synthesis of nitrogen molecules.

Degree: Docteur es, Chimie, 2015, Université Paris-Sud – Paris XI

Les ressources carbonées fossiles (pétrole, charbon, gaz) couvrent 85 % des besoins énergétiques mondiaux et servent de matières premières pour 95 % des consommables chimiques… (more)

Subjects/Keywords: CO2; Amines; Organocatalyse; Réduction; Hydrosilylation; Hydroboration; CO2; Amines; Organocatalysis; Reduction; Hydrosilylation; Hydroboration

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APA (6th Edition):

Blondiaux, E. (2015). Recyclage du CO2 : Une alternative à la pétrochimie pour la synthèse de molécules azotées : CO2 recycling : An alternative to petrochemistry for synthesis of nitrogen molecules. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2015PA112151

Chicago Manual of Style (16th Edition):

Blondiaux, Enguerrand. “Recyclage du CO2 : Une alternative à la pétrochimie pour la synthèse de molécules azotées : CO2 recycling : An alternative to petrochemistry for synthesis of nitrogen molecules.” 2015. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed October 22, 2019. http://www.theses.fr/2015PA112151.

MLA Handbook (7th Edition):

Blondiaux, Enguerrand. “Recyclage du CO2 : Une alternative à la pétrochimie pour la synthèse de molécules azotées : CO2 recycling : An alternative to petrochemistry for synthesis of nitrogen molecules.” 2015. Web. 22 Oct 2019.

Vancouver:

Blondiaux E. Recyclage du CO2 : Une alternative à la pétrochimie pour la synthèse de molécules azotées : CO2 recycling : An alternative to petrochemistry for synthesis of nitrogen molecules. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2015. [cited 2019 Oct 22]. Available from: http://www.theses.fr/2015PA112151.

Council of Science Editors:

Blondiaux E. Recyclage du CO2 : Une alternative à la pétrochimie pour la synthèse de molécules azotées : CO2 recycling : An alternative to petrochemistry for synthesis of nitrogen molecules. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2015. Available from: http://www.theses.fr/2015PA112151


Durham University

10. Douglas, Craig. Silacycles : novel reagents in asymmetric synthesis.

Degree: PhD, 1998, Durham University

 Silicon based organic reagents have enjoyed a wealth of applications in the last thirty year. However, the development of organosilanes for asymmetric synthesis has been… (more)

Subjects/Keywords: 547; Organosilicon; Hydroboration; Divinylsilanes

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APA (6th Edition):

Douglas, C. (1998). Silacycles : novel reagents in asymmetric synthesis. (Doctoral Dissertation). Durham University. Retrieved from http://etheses.dur.ac.uk/4785/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.266505

Chicago Manual of Style (16th Edition):

Douglas, Craig. “Silacycles : novel reagents in asymmetric synthesis.” 1998. Doctoral Dissertation, Durham University. Accessed October 22, 2019. http://etheses.dur.ac.uk/4785/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.266505.

MLA Handbook (7th Edition):

Douglas, Craig. “Silacycles : novel reagents in asymmetric synthesis.” 1998. Web. 22 Oct 2019.

Vancouver:

Douglas C. Silacycles : novel reagents in asymmetric synthesis. [Internet] [Doctoral dissertation]. Durham University; 1998. [cited 2019 Oct 22]. Available from: http://etheses.dur.ac.uk/4785/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.266505.

Council of Science Editors:

Douglas C. Silacycles : novel reagents in asymmetric synthesis. [Doctoral Dissertation]. Durham University; 1998. Available from: http://etheses.dur.ac.uk/4785/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.266505

11. Ferrand, Laura. Hydrofonctionnalisations de liaisons multiples carbone-carbone catalysées par des complexes à base de métaux non nobles : Non-noble metal complexes catalyzed hydrofunctionalization reactions of carbon-carbon multiple bonds.

Degree: Docteur es, Chimie Moléculaire, 2017, Université Pierre et Marie Curie – Paris VI

Ce travail de thèse est consacré au développement de nouvelles méthodologies en catalyse mettant en jeu des complexes métalliques à base de métaux non nobles,… (more)

Subjects/Keywords: Catalyse; Cobalt; Énantiosélectivité; Hydroalkoxylation; Hydroboration; Niobium; Catalysis; Niobium; Hydroalkoxylation; 541.2

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APA (6th Edition):

Ferrand, L. (2017). Hydrofonctionnalisations de liaisons multiples carbone-carbone catalysées par des complexes à base de métaux non nobles : Non-noble metal complexes catalyzed hydrofunctionalization reactions of carbon-carbon multiple bonds. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2017PA066348

Chicago Manual of Style (16th Edition):

Ferrand, Laura. “Hydrofonctionnalisations de liaisons multiples carbone-carbone catalysées par des complexes à base de métaux non nobles : Non-noble metal complexes catalyzed hydrofunctionalization reactions of carbon-carbon multiple bonds.” 2017. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed October 22, 2019. http://www.theses.fr/2017PA066348.

MLA Handbook (7th Edition):

Ferrand, Laura. “Hydrofonctionnalisations de liaisons multiples carbone-carbone catalysées par des complexes à base de métaux non nobles : Non-noble metal complexes catalyzed hydrofunctionalization reactions of carbon-carbon multiple bonds.” 2017. Web. 22 Oct 2019.

Vancouver:

Ferrand L. Hydrofonctionnalisations de liaisons multiples carbone-carbone catalysées par des complexes à base de métaux non nobles : Non-noble metal complexes catalyzed hydrofunctionalization reactions of carbon-carbon multiple bonds. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2017. [cited 2019 Oct 22]. Available from: http://www.theses.fr/2017PA066348.

Council of Science Editors:

Ferrand L. Hydrofonctionnalisations de liaisons multiples carbone-carbone catalysées par des complexes à base de métaux non nobles : Non-noble metal complexes catalyzed hydrofunctionalization reactions of carbon-carbon multiple bonds. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2017. Available from: http://www.theses.fr/2017PA066348


University of Victoria

12. Theron, Robin. Real-time Investigation of Catalytic Reaction Mechanisms by Mass Spectrometry and Infrared Spectroscopy.

Degree: Department of Chemistry, 2015, University of Victoria

 Electrospray ionization mass spectrometry (ESI-MS) has been applied to the realtime study of homogeneous organometallic reactions. ESI-MS as a soft ionization technique is amenable to… (more)

Subjects/Keywords: Mass spectormetry; Infrared spectroscopy; Catalysis; Chemistry; operando spectroscopy; hydroacylation; hydrogenation; hydroboration

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APA (6th Edition):

Theron, R. (2015). Real-time Investigation of Catalytic Reaction Mechanisms by Mass Spectrometry and Infrared Spectroscopy. (Masters Thesis). University of Victoria. Retrieved from http://hdl.handle.net/1828/6322

Chicago Manual of Style (16th Edition):

Theron, Robin. “Real-time Investigation of Catalytic Reaction Mechanisms by Mass Spectrometry and Infrared Spectroscopy.” 2015. Masters Thesis, University of Victoria. Accessed October 22, 2019. http://hdl.handle.net/1828/6322.

MLA Handbook (7th Edition):

Theron, Robin. “Real-time Investigation of Catalytic Reaction Mechanisms by Mass Spectrometry and Infrared Spectroscopy.” 2015. Web. 22 Oct 2019.

Vancouver:

Theron R. Real-time Investigation of Catalytic Reaction Mechanisms by Mass Spectrometry and Infrared Spectroscopy. [Internet] [Masters thesis]. University of Victoria; 2015. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1828/6322.

Council of Science Editors:

Theron R. Real-time Investigation of Catalytic Reaction Mechanisms by Mass Spectrometry and Infrared Spectroscopy. [Masters Thesis]. University of Victoria; 2015. Available from: http://hdl.handle.net/1828/6322


Georgia Tech

13. Hoyt, Caroline B. Design of polymer architectures for catalysis.

Degree: PhD, Chemistry and Biochemistry, 2017, Georgia Tech

 Polymer structures provide tunable platforms for catalyst design due to the high degree of structural control possible in their synthesis. In this study, several different… (more)

Subjects/Keywords: Polymers; Catalyst; Cooperative catalysis; Hydroboration; Micelle; C-H arylation; Cascade catalysis

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APA (6th Edition):

Hoyt, C. B. (2017). Design of polymer architectures for catalysis. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/60703

Chicago Manual of Style (16th Edition):

Hoyt, Caroline B. “Design of polymer architectures for catalysis.” 2017. Doctoral Dissertation, Georgia Tech. Accessed October 22, 2019. http://hdl.handle.net/1853/60703.

MLA Handbook (7th Edition):

Hoyt, Caroline B. “Design of polymer architectures for catalysis.” 2017. Web. 22 Oct 2019.

Vancouver:

Hoyt CB. Design of polymer architectures for catalysis. [Internet] [Doctoral dissertation]. Georgia Tech; 2017. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1853/60703.

Council of Science Editors:

Hoyt CB. Design of polymer architectures for catalysis. [Doctoral Dissertation]. Georgia Tech; 2017. Available from: http://hdl.handle.net/1853/60703


University of South Florida

14. Motika, Stephen. Diversifying Homogenous Au(I)-Catalysis through New Reaction Discovery.

Degree: 2017, University of South Florida

 Homogenous Au(I)-catalysis has become a valuable synthetic tool to activate a host of unsaturated carbon functional groups towards nucleophilic addition. Over the course of the… (more)

Subjects/Keywords: Gold Catalysis; Dual Catalysis; Hydroboration; 1,2-Azaborine; Chemistry

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APA (6th Edition):

Motika, S. (2017). Diversifying Homogenous Au(I)-Catalysis through New Reaction Discovery. (Thesis). University of South Florida. Retrieved from https://scholarcommons.usf.edu/etd/6911

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):

Motika, Stephen. “Diversifying Homogenous Au(I)-Catalysis through New Reaction Discovery.” 2017. Thesis, University of South Florida. Accessed October 22, 2019. https://scholarcommons.usf.edu/etd/6911.

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

MLA Handbook (7th Edition):

Motika, Stephen. “Diversifying Homogenous Au(I)-Catalysis through New Reaction Discovery.” 2017. Web. 22 Oct 2019.

Vancouver:

Motika S. Diversifying Homogenous Au(I)-Catalysis through New Reaction Discovery. [Internet] [Thesis]. University of South Florida; 2017. [cited 2019 Oct 22]. Available from: https://scholarcommons.usf.edu/etd/6911.

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

Council of Science Editors:

Motika S. Diversifying Homogenous Au(I)-Catalysis through New Reaction Discovery. [Thesis]. University of South Florida; 2017. Available from: https://scholarcommons.usf.edu/etd/6911

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


Rochester Institute of Technology

15. Gillman, Kevin W. Hydroboration of strained cyclopropane ring systems promoted by Wilkinson's catalyst.

Degree: School of Chemistry and Materials Science (COS), 1991, Rochester Institute of Technology

None provided. Advisors/Committee Members: Morrill, Terence.

Subjects/Keywords: Hydroboration; Metal catalysts; Cyclopropane

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APA (6th Edition):

Gillman, K. W. (1991). Hydroboration of strained cyclopropane ring systems promoted by Wilkinson's catalyst. (Thesis). Rochester Institute of Technology. Retrieved from https://scholarworks.rit.edu/theses/5982

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):

Gillman, Kevin W. “Hydroboration of strained cyclopropane ring systems promoted by Wilkinson's catalyst.” 1991. Thesis, Rochester Institute of Technology. Accessed October 22, 2019. https://scholarworks.rit.edu/theses/5982.

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

MLA Handbook (7th Edition):

Gillman, Kevin W. “Hydroboration of strained cyclopropane ring systems promoted by Wilkinson's catalyst.” 1991. Web. 22 Oct 2019.

Vancouver:

Gillman KW. Hydroboration of strained cyclopropane ring systems promoted by Wilkinson's catalyst. [Internet] [Thesis]. Rochester Institute of Technology; 1991. [cited 2019 Oct 22]. Available from: https://scholarworks.rit.edu/theses/5982.

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

Council of Science Editors:

Gillman KW. Hydroboration of strained cyclopropane ring systems promoted by Wilkinson's catalyst. [Thesis]. Rochester Institute of Technology; 1991. Available from: https://scholarworks.rit.edu/theses/5982

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


Boston College

16. Yu, Zhiyong. Total Synthesis of (+)-Discodermolide by Catalytic Stereoselective Borylation Reactions.

Degree: PhD, Chemistry, 2014, Boston College

 (+)-Discodermolide is a marine natural product and is one of the most potent microtubule stabilizers in human cell lines. Because of its unique linear structure… (more)

Subjects/Keywords: asymmetric catalysis; discodermolide; hydroboration; hydroformylation; multi-component coupling; total synthesis

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APA (6th Edition):

Yu, Z. (2014). Total Synthesis of (+)-Discodermolide by Catalytic Stereoselective Borylation Reactions. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:103737

Chicago Manual of Style (16th Edition):

Yu, Zhiyong. “Total Synthesis of (+)-Discodermolide by Catalytic Stereoselective Borylation Reactions.” 2014. Doctoral Dissertation, Boston College. Accessed October 22, 2019. http://dlib.bc.edu/islandora/object/bc-ir:103737.

MLA Handbook (7th Edition):

Yu, Zhiyong. “Total Synthesis of (+)-Discodermolide by Catalytic Stereoselective Borylation Reactions.” 2014. Web. 22 Oct 2019.

Vancouver:

Yu Z. Total Synthesis of (+)-Discodermolide by Catalytic Stereoselective Borylation Reactions. [Internet] [Doctoral dissertation]. Boston College; 2014. [cited 2019 Oct 22]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:103737.

Council of Science Editors:

Yu Z. Total Synthesis of (+)-Discodermolide by Catalytic Stereoselective Borylation Reactions. [Doctoral Dissertation]. Boston College; 2014. Available from: http://dlib.bc.edu/islandora/object/bc-ir:103737


Boston College

17. Lee, Yunmi. Site- and Enantioselective C-C and C-B Bond Forming Reactions Catalyzed by Cu-, Mg-, Zn-, or Al-based N-Heterocyclic Carbene Complexes.

Degree: PhD, Chemistry, 2010, Boston College

 Chapter 1. In this chapter, the ability of chiral bidentate N-heterocyclic carbenes (NHCs) to activate alkylmetal reagents directly in order to promote C‒C bond forming… (more)

Subjects/Keywords: Cu-catalyzed reaction; Dihydroboration; Enantioselective Allylic Alkylation; Hydroboration; N-Heterocyclic carbene

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APA (6th Edition):

Lee, Y. (2010). Site- and Enantioselective C-C and C-B Bond Forming Reactions Catalyzed by Cu-, Mg-, Zn-, or Al-based N-Heterocyclic Carbene Complexes. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:101999

Chicago Manual of Style (16th Edition):

Lee, Yunmi. “Site- and Enantioselective C-C and C-B Bond Forming Reactions Catalyzed by Cu-, Mg-, Zn-, or Al-based N-Heterocyclic Carbene Complexes.” 2010. Doctoral Dissertation, Boston College. Accessed October 22, 2019. http://dlib.bc.edu/islandora/object/bc-ir:101999.

MLA Handbook (7th Edition):

Lee, Yunmi. “Site- and Enantioselective C-C and C-B Bond Forming Reactions Catalyzed by Cu-, Mg-, Zn-, or Al-based N-Heterocyclic Carbene Complexes.” 2010. Web. 22 Oct 2019.

Vancouver:

Lee Y. Site- and Enantioselective C-C and C-B Bond Forming Reactions Catalyzed by Cu-, Mg-, Zn-, or Al-based N-Heterocyclic Carbene Complexes. [Internet] [Doctoral dissertation]. Boston College; 2010. [cited 2019 Oct 22]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101999.

Council of Science Editors:

Lee Y. Site- and Enantioselective C-C and C-B Bond Forming Reactions Catalyzed by Cu-, Mg-, Zn-, or Al-based N-Heterocyclic Carbene Complexes. [Doctoral Dissertation]. Boston College; 2010. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101999


University of Adelaide

18. Marshall, Philip Andrew. Approaches to the synthesis of Phthalideisquinolines [sic] and synthesis and hydroboration of benzocyclene oxides.

Degree: 1978, University of Adelaide

Subjects/Keywords: Isoquinoline.; Alkaloids.; Benzocyclenes.; Hydroboration.

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APA (6th Edition):

Marshall, P. A. (1978). Approaches to the synthesis of Phthalideisquinolines [sic] and synthesis and hydroboration of benzocyclene oxides. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/20256

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):

Marshall, Philip Andrew. “Approaches to the synthesis of Phthalideisquinolines [sic] and synthesis and hydroboration of benzocyclene oxides.” 1978. Thesis, University of Adelaide. Accessed October 22, 2019. http://hdl.handle.net/2440/20256.

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

MLA Handbook (7th Edition):

Marshall, Philip Andrew. “Approaches to the synthesis of Phthalideisquinolines [sic] and synthesis and hydroboration of benzocyclene oxides.” 1978. Web. 22 Oct 2019.

Vancouver:

Marshall PA. Approaches to the synthesis of Phthalideisquinolines [sic] and synthesis and hydroboration of benzocyclene oxides. [Internet] [Thesis]. University of Adelaide; 1978. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/2440/20256.

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

Council of Science Editors:

Marshall PA. Approaches to the synthesis of Phthalideisquinolines [sic] and synthesis and hydroboration of benzocyclene oxides. [Thesis]. University of Adelaide; 1978. Available from: http://hdl.handle.net/2440/20256

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


Queens University

19. Edwards, David Ryan. A Study of Rhodium Catalyzed Hydroborations and Sulfur ylide Epoxidations .

Degree: Chemistry, 2007, Queens University

 A rhodium-catalyzed process has been developed in which mixtures of internal and terminal olefins are isomerized and hydroborated in one step yielding the corresponding terminal… (more)

Subjects/Keywords: Sulfur ylide; Epoxidation; Hydroboration; Regioselectivity

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APA (6th Edition):

Edwards, D. R. (2007). A Study of Rhodium Catalyzed Hydroborations and Sulfur ylide Epoxidations . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/681

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):

Edwards, David Ryan. “A Study of Rhodium Catalyzed Hydroborations and Sulfur ylide Epoxidations .” 2007. Thesis, Queens University. Accessed October 22, 2019. http://hdl.handle.net/1974/681.

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

MLA Handbook (7th Edition):

Edwards, David Ryan. “A Study of Rhodium Catalyzed Hydroborations and Sulfur ylide Epoxidations .” 2007. Web. 22 Oct 2019.

Vancouver:

Edwards DR. A Study of Rhodium Catalyzed Hydroborations and Sulfur ylide Epoxidations . [Internet] [Thesis]. Queens University; 2007. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1974/681.

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

Council of Science Editors:

Edwards DR. A Study of Rhodium Catalyzed Hydroborations and Sulfur ylide Epoxidations . [Thesis]. Queens University; 2007. Available from: http://hdl.handle.net/1974/681

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


University of Kansas

20. Edwards, Andrew. Stereoselective Additions to Cyclopropenes.

Degree: PhD, Chemistry, 2018, University of Kansas

 This thesis concerns strain-release driven stereoselective addition reactions to cyclopropenes leading to the synthesis of medium-sized 8-membered 1,5-dioxocane ring structures, optically active cyclopropylboronates, and densely… (more)

Subjects/Keywords: Organic chemistry; Carbomagnesiation; Catalytic; Cyclopropene; Directed; Hydroboration; Stereoselective

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APA (6th Edition):

Edwards, A. (2018). Stereoselective Additions to Cyclopropenes. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/27877

Chicago Manual of Style (16th Edition):

Edwards, Andrew. “Stereoselective Additions to Cyclopropenes.” 2018. Doctoral Dissertation, University of Kansas. Accessed October 22, 2019. http://hdl.handle.net/1808/27877.

MLA Handbook (7th Edition):

Edwards, Andrew. “Stereoselective Additions to Cyclopropenes.” 2018. Web. 22 Oct 2019.

Vancouver:

Edwards A. Stereoselective Additions to Cyclopropenes. [Internet] [Doctoral dissertation]. University of Kansas; 2018. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1808/27877.

Council of Science Editors:

Edwards A. Stereoselective Additions to Cyclopropenes. [Doctoral Dissertation]. University of Kansas; 2018. Available from: http://hdl.handle.net/1808/27877


University of Bath

21. Fordred, Paul. Synthetically useful alkene isomerisation and hydroboration reactions.

Degree: PhD, 2012, University of Bath

 Upon treatment with a palladium catalyst and hydrogen gas in the presence of caesium carbonate, a wide range of exomethylenic allylic alcohols were found to… (more)

Subjects/Keywords: 547; isomerisation; allylic alcohol; palladium; hydroboration; asymmetric; diols

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APA (6th Edition):

Fordred, P. (2012). Synthetically useful alkene isomerisation and hydroboration reactions. (Doctoral Dissertation). University of Bath. Retrieved from https://researchportal.bath.ac.uk/en/studentthesis/synthetically-useful-alkene-isomerisation-and-hydroboration-reactions(1a927741-9827-4942-be7c-93249d6eaf8c).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.558880

Chicago Manual of Style (16th Edition):

Fordred, Paul. “Synthetically useful alkene isomerisation and hydroboration reactions.” 2012. Doctoral Dissertation, University of Bath. Accessed October 22, 2019. https://researchportal.bath.ac.uk/en/studentthesis/synthetically-useful-alkene-isomerisation-and-hydroboration-reactions(1a927741-9827-4942-be7c-93249d6eaf8c).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.558880.

MLA Handbook (7th Edition):

Fordred, Paul. “Synthetically useful alkene isomerisation and hydroboration reactions.” 2012. Web. 22 Oct 2019.

Vancouver:

Fordred P. Synthetically useful alkene isomerisation and hydroboration reactions. [Internet] [Doctoral dissertation]. University of Bath; 2012. [cited 2019 Oct 22]. Available from: https://researchportal.bath.ac.uk/en/studentthesis/synthetically-useful-alkene-isomerisation-and-hydroboration-reactions(1a927741-9827-4942-be7c-93249d6eaf8c).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.558880.

Council of Science Editors:

Fordred P. Synthetically useful alkene isomerisation and hydroboration reactions. [Doctoral Dissertation]. University of Bath; 2012. Available from: https://researchportal.bath.ac.uk/en/studentthesis/synthetically-useful-alkene-isomerisation-and-hydroboration-reactions(1a927741-9827-4942-be7c-93249d6eaf8c).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.558880


University of Arizona

22. Piepgrass, Kent Wesley. THE HYDROBORATION OF 7-AZAINDOLE, 1,8-NAPHTHYRIDINE, AND THEIR N-METHYLATED DERIVATIVES.

Degree: 1982, University of Arizona

Subjects/Keywords: Hydroboration.; Organoboron compounds.; Aromatic compounds.

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APA (6th Edition):

Piepgrass, K. W. (1982). THE HYDROBORATION OF 7-AZAINDOLE, 1,8-NAPHTHYRIDINE, AND THEIR N-METHYLATED DERIVATIVES. (Masters Thesis). University of Arizona. Retrieved from http://hdl.handle.net/10150/274634

Chicago Manual of Style (16th Edition):

Piepgrass, Kent Wesley. “THE HYDROBORATION OF 7-AZAINDOLE, 1,8-NAPHTHYRIDINE, AND THEIR N-METHYLATED DERIVATIVES. ” 1982. Masters Thesis, University of Arizona. Accessed October 22, 2019. http://hdl.handle.net/10150/274634.

MLA Handbook (7th Edition):

Piepgrass, Kent Wesley. “THE HYDROBORATION OF 7-AZAINDOLE, 1,8-NAPHTHYRIDINE, AND THEIR N-METHYLATED DERIVATIVES. ” 1982. Web. 22 Oct 2019.

Vancouver:

Piepgrass KW. THE HYDROBORATION OF 7-AZAINDOLE, 1,8-NAPHTHYRIDINE, AND THEIR N-METHYLATED DERIVATIVES. [Internet] [Masters thesis]. University of Arizona; 1982. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/10150/274634.

Council of Science Editors:

Piepgrass KW. THE HYDROBORATION OF 7-AZAINDOLE, 1,8-NAPHTHYRIDINE, AND THEIR N-METHYLATED DERIVATIVES. [Masters Thesis]. University of Arizona; 1982. Available from: http://hdl.handle.net/10150/274634

23. Wolff, Niklas von. Reaction mechanisms of CO₂ activation and catalytic reduction : Mécanismes réactionnels d’activation et de réduction catalytique du CO₂.

Degree: Docteur es, Chimie, 2016, Paris Saclay

L’utilisation du dioxyde de carbone (CO₂) comme source de composés C1 pour la chimie fine est intéressante d’un point de vue économique et pour des… (more)

Subjects/Keywords: Mécanismes réactionnels; Hydroboration catalytique; Recyclage du CO2; Dioxyde de carbone; DFT; Synthèse de sulfone; Dioxyde de soufre; Reaction mechanisms; Catalytic hydroboration; CO2 recycling; Carbon dioxide; DFT; Sulfone synthesis; Sulfur dioxide

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APA (6th Edition):

Wolff, N. v. (2016). Reaction mechanisms of CO₂ activation and catalytic reduction : Mécanismes réactionnels d’activation et de réduction catalytique du CO₂. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2016SACLS580

Chicago Manual of Style (16th Edition):

Wolff, Niklas von. “Reaction mechanisms of CO₂ activation and catalytic reduction : Mécanismes réactionnels d’activation et de réduction catalytique du CO₂.” 2016. Doctoral Dissertation, Paris Saclay. Accessed October 22, 2019. http://www.theses.fr/2016SACLS580.

MLA Handbook (7th Edition):

Wolff, Niklas von. “Reaction mechanisms of CO₂ activation and catalytic reduction : Mécanismes réactionnels d’activation et de réduction catalytique du CO₂.” 2016. Web. 22 Oct 2019.

Vancouver:

Wolff Nv. Reaction mechanisms of CO₂ activation and catalytic reduction : Mécanismes réactionnels d’activation et de réduction catalytique du CO₂. [Internet] [Doctoral dissertation]. Paris Saclay; 2016. [cited 2019 Oct 22]. Available from: http://www.theses.fr/2016SACLS580.

Council of Science Editors:

Wolff Nv. Reaction mechanisms of CO₂ activation and catalytic reduction : Mécanismes réactionnels d’activation et de réduction catalytique du CO₂. [Doctoral Dissertation]. Paris Saclay; 2016. Available from: http://www.theses.fr/2016SACLS580

24. Chauvier, Clément. Nouvelles réactions d'hydroboration et d'hydrosilylation par transfert avec des réducteurs renouvelables à base d'acide formique : Novel Transfer Hydroboration and Hydrosilylation Processes with Formic Acid Based Renewable Reductants.

Degree: Docteur es, Chimie, 2017, Paris Saclay

Les ressources fossiles que sont le gaz ou le pétrole permettent non seulement de couvrir la majeure partie des besoins énergétiques mondiaux, mais fournissent également… (more)

Subjects/Keywords: Bore; Acide formique; CO₂; Silicium; Hydroboration; Hydrosilylation; Catalyse homogène; Calculs DFT; Boron; Formic acid; CO₂; Silicon; Hydroboration; Hydrosilylation; Homogenous catalysis; DFT calculations

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APA (6th Edition):

Chauvier, C. (2017). Nouvelles réactions d'hydroboration et d'hydrosilylation par transfert avec des réducteurs renouvelables à base d'acide formique : Novel Transfer Hydroboration and Hydrosilylation Processes with Formic Acid Based Renewable Reductants. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2017SACLS359

Chicago Manual of Style (16th Edition):

Chauvier, Clément. “Nouvelles réactions d'hydroboration et d'hydrosilylation par transfert avec des réducteurs renouvelables à base d'acide formique : Novel Transfer Hydroboration and Hydrosilylation Processes with Formic Acid Based Renewable Reductants.” 2017. Doctoral Dissertation, Paris Saclay. Accessed October 22, 2019. http://www.theses.fr/2017SACLS359.

MLA Handbook (7th Edition):

Chauvier, Clément. “Nouvelles réactions d'hydroboration et d'hydrosilylation par transfert avec des réducteurs renouvelables à base d'acide formique : Novel Transfer Hydroboration and Hydrosilylation Processes with Formic Acid Based Renewable Reductants.” 2017. Web. 22 Oct 2019.

Vancouver:

Chauvier C. Nouvelles réactions d'hydroboration et d'hydrosilylation par transfert avec des réducteurs renouvelables à base d'acide formique : Novel Transfer Hydroboration and Hydrosilylation Processes with Formic Acid Based Renewable Reductants. [Internet] [Doctoral dissertation]. Paris Saclay; 2017. [cited 2019 Oct 22]. Available from: http://www.theses.fr/2017SACLS359.

Council of Science Editors:

Chauvier C. Nouvelles réactions d'hydroboration et d'hydrosilylation par transfert avec des réducteurs renouvelables à base d'acide formique : Novel Transfer Hydroboration and Hydrosilylation Processes with Formic Acid Based Renewable Reductants. [Doctoral Dissertation]. Paris Saclay; 2017. Available from: http://www.theses.fr/2017SACLS359


University of Lund

25. Dahlqvist, Alexander. Novel monogalactoside galectin inhibitor scaffolds : Guiding selectivity with heteroaromatic interactions.

Degree: 2019, University of Lund

 Carbohydrates are involved in many cellular processes, and most biomolecules are glycosylated. Thesemodifications are used in biological systems as information carriers, helping regulate organization on… (more)

Subjects/Keywords: Organisk kemi; Galectin; Galectin inhibitor; Heterocycles; C-glycoside; Medicinal chemistry; Organic chemistry; Hydroboration; Diastereoselective; Galactose

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APA (6th Edition):

Dahlqvist, A. (2019). Novel monogalactoside galectin inhibitor scaffolds : Guiding selectivity with heteroaromatic interactions. (Doctoral Dissertation). University of Lund. Retrieved from http://lup.lub.lu.se/record/56fbe79b-566b-491d-8b05-5af5580c57b6 ; http://portal.research.lu.se/ws/files/63407223/e_spik_alexander_nr2.pdf

Chicago Manual of Style (16th Edition):

Dahlqvist, Alexander. “Novel monogalactoside galectin inhibitor scaffolds : Guiding selectivity with heteroaromatic interactions.” 2019. Doctoral Dissertation, University of Lund. Accessed October 22, 2019. http://lup.lub.lu.se/record/56fbe79b-566b-491d-8b05-5af5580c57b6 ; http://portal.research.lu.se/ws/files/63407223/e_spik_alexander_nr2.pdf.

MLA Handbook (7th Edition):

Dahlqvist, Alexander. “Novel monogalactoside galectin inhibitor scaffolds : Guiding selectivity with heteroaromatic interactions.” 2019. Web. 22 Oct 2019.

Vancouver:

Dahlqvist A. Novel monogalactoside galectin inhibitor scaffolds : Guiding selectivity with heteroaromatic interactions. [Internet] [Doctoral dissertation]. University of Lund; 2019. [cited 2019 Oct 22]. Available from: http://lup.lub.lu.se/record/56fbe79b-566b-491d-8b05-5af5580c57b6 ; http://portal.research.lu.se/ws/files/63407223/e_spik_alexander_nr2.pdf.

Council of Science Editors:

Dahlqvist A. Novel monogalactoside galectin inhibitor scaffolds : Guiding selectivity with heteroaromatic interactions. [Doctoral Dissertation]. University of Lund; 2019. Available from: http://lup.lub.lu.se/record/56fbe79b-566b-491d-8b05-5af5580c57b6 ; http://portal.research.lu.se/ws/files/63407223/e_spik_alexander_nr2.pdf


University of Toronto

26. Tang, Connie. 1,1-Hydroboration and Borane Adduct of Diphenyldiazomethane.

Degree: 2018, University of Toronto

The advent of frustrated Lewis pair chemistry has demonstrated unique reactivity with a variety of small molecules. This thesis explores related chemistry with reactions of… (more)

Subjects/Keywords: Diazomethane; Dinitrogen; Frustrated Lewis Pair; Hydroboration; Main Group Chemistry; Nitrogen Fixation; 0488

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APA (6th Edition):

Tang, C. (2018). 1,1-Hydroboration and Borane Adduct of Diphenyldiazomethane. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/89495

Chicago Manual of Style (16th Edition):

Tang, Connie. “1,1-Hydroboration and Borane Adduct of Diphenyldiazomethane.” 2018. Masters Thesis, University of Toronto. Accessed October 22, 2019. http://hdl.handle.net/1807/89495.

MLA Handbook (7th Edition):

Tang, Connie. “1,1-Hydroboration and Borane Adduct of Diphenyldiazomethane.” 2018. Web. 22 Oct 2019.

Vancouver:

Tang C. 1,1-Hydroboration and Borane Adduct of Diphenyldiazomethane. [Internet] [Masters thesis]. University of Toronto; 2018. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1807/89495.

Council of Science Editors:

Tang C. 1,1-Hydroboration and Borane Adduct of Diphenyldiazomethane. [Masters Thesis]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/89495


Université de Montréal

27. Ladjel, Chehla. Développement de méthodologies en un seul pot impliquant une réaction de méthylénation : utilisation de complexes d'iridium dans les réactions d'oléfination .

Degree: 2008, Université de Montréal

Subjects/Keywords: Méthylénation; Hydrogénation; Hydroboration; Couplage de Suzuki; Iridium; Oléfination

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APA (6th Edition):

Ladjel, C. (2008). Développement de méthodologies en un seul pot impliquant une réaction de méthylénation : utilisation de complexes d'iridium dans les réactions d'oléfination . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/18004

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):

Ladjel, Chehla. “Développement de méthodologies en un seul pot impliquant une réaction de méthylénation : utilisation de complexes d'iridium dans les réactions d'oléfination .” 2008. Thesis, Université de Montréal. Accessed October 22, 2019. http://hdl.handle.net/1866/18004.

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

MLA Handbook (7th Edition):

Ladjel, Chehla. “Développement de méthodologies en un seul pot impliquant une réaction de méthylénation : utilisation de complexes d'iridium dans les réactions d'oléfination .” 2008. Web. 22 Oct 2019.

Vancouver:

Ladjel C. Développement de méthodologies en un seul pot impliquant une réaction de méthylénation : utilisation de complexes d'iridium dans les réactions d'oléfination . [Internet] [Thesis]. Université de Montréal; 2008. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1866/18004.

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

Council of Science Editors:

Ladjel C. Développement de méthodologies en un seul pot impliquant une réaction de méthylénation : utilisation de complexes d'iridium dans les réactions d'oléfination . [Thesis]. Université de Montréal; 2008. Available from: http://hdl.handle.net/1866/18004

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


Montana State University

28. Lee, Changjoo. Heterocyclic chemistry : unique role of heteroatoms in structure and reactivity.

Degree: College of Letters & Science, 1991, Montana State University

Subjects/Keywords: Heterocyclic chemistry.; Hydroboration.; Propellanes.; Solvolysis.; Heterocyclic compounds.

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

APA (6th Edition):

Lee, C. (1991). Heterocyclic chemistry : unique role of heteroatoms in structure and reactivity. (Thesis). Montana State University. Retrieved from https://scholarworks.montana.edu/xmlui/handle/1/7007

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):

Lee, Changjoo. “Heterocyclic chemistry : unique role of heteroatoms in structure and reactivity.” 1991. Thesis, Montana State University. Accessed October 22, 2019. https://scholarworks.montana.edu/xmlui/handle/1/7007.

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

MLA Handbook (7th Edition):

Lee, Changjoo. “Heterocyclic chemistry : unique role of heteroatoms in structure and reactivity.” 1991. Web. 22 Oct 2019.

Vancouver:

Lee C. Heterocyclic chemistry : unique role of heteroatoms in structure and reactivity. [Internet] [Thesis]. Montana State University; 1991. [cited 2019 Oct 22]. Available from: https://scholarworks.montana.edu/xmlui/handle/1/7007.

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

Council of Science Editors:

Lee C. Heterocyclic chemistry : unique role of heteroatoms in structure and reactivity. [Thesis]. Montana State University; 1991. Available from: https://scholarworks.montana.edu/xmlui/handle/1/7007

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


Universitat Rovira i Virgili

29. Lillo García, Vanesa. Transition metal catalysed functionalisation of c=c through boron chemistry: a tandem approach.

Degree: Departament de Química Física i Inorgànica, 2009, Universitat Rovira i Virgili

 Organoboron compounds are some of the most useful reagents in organic synthesis. The carbon-boron bond, once formed, can be cleaved in a variety of ways,… (more)

Subjects/Keywords: Hydroboration; Diboration; B-addition; Tandem reactions; C-C cross coupling; Carbene; Homogeneous Catalysis; 54; 542; 546

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APA (6th Edition):

Lillo García, V. (2009). Transition metal catalysed functionalisation of c=c through boron chemistry: a tandem approach. (Thesis). Universitat Rovira i Virgili. Retrieved from http://hdl.handle.net/10803/9101

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):

Lillo García, Vanesa. “Transition metal catalysed functionalisation of c=c through boron chemistry: a tandem approach.” 2009. Thesis, Universitat Rovira i Virgili. Accessed October 22, 2019. http://hdl.handle.net/10803/9101.

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

MLA Handbook (7th Edition):

Lillo García, Vanesa. “Transition metal catalysed functionalisation of c=c through boron chemistry: a tandem approach.” 2009. Web. 22 Oct 2019.

Vancouver:

Lillo García V. Transition metal catalysed functionalisation of c=c through boron chemistry: a tandem approach. [Internet] [Thesis]. Universitat Rovira i Virgili; 2009. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/10803/9101.

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

Council of Science Editors:

Lillo García V. Transition metal catalysed functionalisation of c=c through boron chemistry: a tandem approach. [Thesis]. Universitat Rovira i Virgili; 2009. Available from: http://hdl.handle.net/10803/9101

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

30. Meng, Xiangtao. Chemical Modification of Cellulose Esters for Oral Drug Delivery.

Degree: PhD, Learning Sciences and Technologies, 2016, Virginia Tech

 Polymer functional groups have critical impacts upon physical, chemical and mechanical properties, and thus affect the specific applications of the polymer. Functionalization of cellulose esters… (more)

Subjects/Keywords: cellulose esters; functionalization; amorphous solid dispersion; olefin metathesis; thiol-Michael addition; esterification; hydroboration oxidation; click reaction.

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

APA (6th Edition):

Meng, X. (2016). Chemical Modification of Cellulose Esters for Oral Drug Delivery. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/71383

Chicago Manual of Style (16th Edition):

Meng, Xiangtao. “Chemical Modification of Cellulose Esters for Oral Drug Delivery.” 2016. Doctoral Dissertation, Virginia Tech. Accessed October 22, 2019. http://hdl.handle.net/10919/71383.

MLA Handbook (7th Edition):

Meng, Xiangtao. “Chemical Modification of Cellulose Esters for Oral Drug Delivery.” 2016. Web. 22 Oct 2019.

Vancouver:

Meng X. Chemical Modification of Cellulose Esters for Oral Drug Delivery. [Internet] [Doctoral dissertation]. Virginia Tech; 2016. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/10919/71383.

Council of Science Editors:

Meng X. Chemical Modification of Cellulose Esters for Oral Drug Delivery. [Doctoral Dissertation]. Virginia Tech; 2016. Available from: http://hdl.handle.net/10919/71383

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