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You searched for subject:(borylation). Showing records 1 – 30 of 53 total matches.

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University of Pennsylvania

1. Cavalcanti, Livia. Potassium Organotrifluoroborates: Chemistry Beyond Cross-Coupling.

Degree: 2013, University of Pennsylvania

 Over the years, organoboron species have been vastly utilized in synthetic organic chemistry. Traditional methods to synthesize these compounds, such as metal-halogen exchange, C-H activation… (more)

Subjects/Keywords: BORYLATION; ORGANOTRIFLUOROBORATES; REACTIVITY; Chemistry

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APA (6th Edition):

Cavalcanti, L. (2013). Potassium Organotrifluoroborates: Chemistry Beyond Cross-Coupling. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/741

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):

Cavalcanti, Livia. “Potassium Organotrifluoroborates: Chemistry Beyond Cross-Coupling.” 2013. Thesis, University of Pennsylvania. Accessed September 21, 2019. https://repository.upenn.edu/edissertations/741.

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

MLA Handbook (7th Edition):

Cavalcanti, Livia. “Potassium Organotrifluoroborates: Chemistry Beyond Cross-Coupling.” 2013. Web. 21 Sep 2019.

Vancouver:

Cavalcanti L. Potassium Organotrifluoroborates: Chemistry Beyond Cross-Coupling. [Internet] [Thesis]. University of Pennsylvania; 2013. [cited 2019 Sep 21]. Available from: https://repository.upenn.edu/edissertations/741.

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

Council of Science Editors:

Cavalcanti L. Potassium Organotrifluoroborates: Chemistry Beyond Cross-Coupling. [Thesis]. University of Pennsylvania; 2013. Available from: https://repository.upenn.edu/edissertations/741

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


University of Michigan

2. Schimler, Sydonie. Development of Practical Fluorination Methods and Selective C-H Borylation of Methane.

Degree: PhD, Chemistry, 2017, University of Michigan

 Fluorinated (hetero)arenes are finding increasing importance in pharmaceuticals and agrochemicals. As a result, the development of mild, inexpensive, and practical methods for the formation of… (more)

Subjects/Keywords: Fluorination; Borylation; Chemistry; Science

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APA (6th Edition):

Schimler, S. (2017). Development of Practical Fluorination Methods and Selective C-H Borylation of Methane. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/138679

Chicago Manual of Style (16th Edition):

Schimler, Sydonie. “Development of Practical Fluorination Methods and Selective C-H Borylation of Methane.” 2017. Doctoral Dissertation, University of Michigan. Accessed September 21, 2019. http://hdl.handle.net/2027.42/138679.

MLA Handbook (7th Edition):

Schimler, Sydonie. “Development of Practical Fluorination Methods and Selective C-H Borylation of Methane.” 2017. Web. 21 Sep 2019.

Vancouver:

Schimler S. Development of Practical Fluorination Methods and Selective C-H Borylation of Methane. [Internet] [Doctoral dissertation]. University of Michigan; 2017. [cited 2019 Sep 21]. Available from: http://hdl.handle.net/2027.42/138679.

Council of Science Editors:

Schimler S. Development of Practical Fluorination Methods and Selective C-H Borylation of Methane. [Doctoral Dissertation]. University of Michigan; 2017. Available from: http://hdl.handle.net/2027.42/138679


University of Manchester

3. Del Grosso, Alessandro. Borenium cations for the direct electrophilic borylation of arenes.

Degree: PhD, 2013, University of Manchester

 A catalytic (in Brønsted superacid) and a stoichiometric process were developed to synthesise aryl boronic esters with boron cations via electrophilic arene borylation. The treatment… (more)

Subjects/Keywords: 547; borenium; borocation; borylation; boronic ester; boronate ester; electrophilic borylation

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APA (6th Edition):

Del Grosso, A. (2013). Borenium cations for the direct electrophilic borylation of arenes. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/borenium-cations-for-the-direct-electrophilic-borylation-of-arenes(a505cdb2-08fe-43a0-ad0b-86ab357fadd1).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.570285

Chicago Manual of Style (16th Edition):

Del Grosso, Alessandro. “Borenium cations for the direct electrophilic borylation of arenes.” 2013. Doctoral Dissertation, University of Manchester. Accessed September 21, 2019. https://www.research.manchester.ac.uk/portal/en/theses/borenium-cations-for-the-direct-electrophilic-borylation-of-arenes(a505cdb2-08fe-43a0-ad0b-86ab357fadd1).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.570285.

MLA Handbook (7th Edition):

Del Grosso, Alessandro. “Borenium cations for the direct electrophilic borylation of arenes.” 2013. Web. 21 Sep 2019.

Vancouver:

Del Grosso A. Borenium cations for the direct electrophilic borylation of arenes. [Internet] [Doctoral dissertation]. University of Manchester; 2013. [cited 2019 Sep 21]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/borenium-cations-for-the-direct-electrophilic-borylation-of-arenes(a505cdb2-08fe-43a0-ad0b-86ab357fadd1).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.570285.

Council of Science Editors:

Del Grosso A. Borenium cations for the direct electrophilic borylation of arenes. [Doctoral Dissertation]. University of Manchester; 2013. Available from: https://www.research.manchester.ac.uk/portal/en/theses/borenium-cations-for-the-direct-electrophilic-borylation-of-arenes(a505cdb2-08fe-43a0-ad0b-86ab357fadd1).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.570285


University of Alberta

4. Kim, You-Ri. Optimization and Applications of the Catalytic Enantioselective Borylative Migration of Functionalized Piperidines.

Degree: MS, Department of Chemistry, 2016, University of Alberta

 The catalytic enantioselective borylative migration developed in 2009 by our laboratory is a convenient, single-step method that provides enantiomerically enriched heterocyclic allylboronates. However, this chemistry… (more)

Subjects/Keywords: Piperidine; Borylation; Allylboronate; Allylboration; Chiral piperidine

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APA (6th Edition):

Kim, Y. (2016). Optimization and Applications of the Catalytic Enantioselective Borylative Migration of Functionalized Piperidines. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/c4m90dv69q

Chicago Manual of Style (16th Edition):

Kim, You-Ri. “Optimization and Applications of the Catalytic Enantioselective Borylative Migration of Functionalized Piperidines.” 2016. Masters Thesis, University of Alberta. Accessed September 21, 2019. https://era.library.ualberta.ca/files/c4m90dv69q.

MLA Handbook (7th Edition):

Kim, You-Ri. “Optimization and Applications of the Catalytic Enantioselective Borylative Migration of Functionalized Piperidines.” 2016. Web. 21 Sep 2019.

Vancouver:

Kim Y. Optimization and Applications of the Catalytic Enantioselective Borylative Migration of Functionalized Piperidines. [Internet] [Masters thesis]. University of Alberta; 2016. [cited 2019 Sep 21]. Available from: https://era.library.ualberta.ca/files/c4m90dv69q.

Council of Science Editors:

Kim Y. Optimization and Applications of the Catalytic Enantioselective Borylative Migration of Functionalized Piperidines. [Masters Thesis]. University of Alberta; 2016. Available from: https://era.library.ualberta.ca/files/c4m90dv69q


Boston College

5. Xiao, Lu. Copper-Catalyzed Borylation of Hemiaminal Ethers and Ruthenium-Catalyzed Tandem Reactions of Nitrogen-Tethered Dienes.

Degree: PhD, Chemistry, 2016, Boston College

 Chapter 1 Bisphosphine monoxides have unique coordinating capabilities with transition metals. Several research groups have independently reported transition metal-catalyzed highly stereoselective reactions by using chiral… (more)

Subjects/Keywords: Borylation; Catalysis; Copper; Ruthenium; Tandem Reactions

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APA (6th Edition):

Xiao, L. (2016). Copper-Catalyzed Borylation of Hemiaminal Ethers and Ruthenium-Catalyzed Tandem Reactions of Nitrogen-Tethered Dienes. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:107234

Chicago Manual of Style (16th Edition):

Xiao, Lu. “Copper-Catalyzed Borylation of Hemiaminal Ethers and Ruthenium-Catalyzed Tandem Reactions of Nitrogen-Tethered Dienes.” 2016. Doctoral Dissertation, Boston College. Accessed September 21, 2019. http://dlib.bc.edu/islandora/object/bc-ir:107234.

MLA Handbook (7th Edition):

Xiao, Lu. “Copper-Catalyzed Borylation of Hemiaminal Ethers and Ruthenium-Catalyzed Tandem Reactions of Nitrogen-Tethered Dienes.” 2016. Web. 21 Sep 2019.

Vancouver:

Xiao L. Copper-Catalyzed Borylation of Hemiaminal Ethers and Ruthenium-Catalyzed Tandem Reactions of Nitrogen-Tethered Dienes. [Internet] [Doctoral dissertation]. Boston College; 2016. [cited 2019 Sep 21]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:107234.

Council of Science Editors:

Xiao L. Copper-Catalyzed Borylation of Hemiaminal Ethers and Ruthenium-Catalyzed Tandem Reactions of Nitrogen-Tethered Dienes. [Doctoral Dissertation]. Boston College; 2016. Available from: http://dlib.bc.edu/islandora/object/bc-ir:107234


University of California – San Diego

6. Romero, Erik Anthony. Taming Carbene Copper(I)-Hydride Complexes.

Degree: Chemistry and Biochemistry, 2019, University of California – San Diego

 Although initially reported in 1844, copper(I)-hydrides were not widely studied until the isolation of “Stryker’s reagent” in 1971. Following this development, researchers reported a myriad… (more)

Subjects/Keywords: Inorganic chemistry; borylation; carbene; copper; hydride; monomer

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APA (6th Edition):

Romero, E. A. (2019). Taming Carbene Copper(I)-Hydride Complexes. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/0574f1cg

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):

Romero, Erik Anthony. “Taming Carbene Copper(I)-Hydride Complexes.” 2019. Thesis, University of California – San Diego. Accessed September 21, 2019. http://www.escholarship.org/uc/item/0574f1cg.

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

MLA Handbook (7th Edition):

Romero, Erik Anthony. “Taming Carbene Copper(I)-Hydride Complexes.” 2019. Web. 21 Sep 2019.

Vancouver:

Romero EA. Taming Carbene Copper(I)-Hydride Complexes. [Internet] [Thesis]. University of California – San Diego; 2019. [cited 2019 Sep 21]. Available from: http://www.escholarship.org/uc/item/0574f1cg.

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

Council of Science Editors:

Romero EA. Taming Carbene Copper(I)-Hydride Complexes. [Thesis]. University of California – San Diego; 2019. Available from: http://www.escholarship.org/uc/item/0574f1cg

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


Princeton University

7. 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 September 21, 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. 21 Sep 2019.

Vancouver:

Obligacion JV. BASE METAL CATALYSIS FOR THE SYNTHESIS OF ORGANOBORON COMPOUNDS . [Internet] [Doctoral dissertation]. Princeton University; 2017. [cited 2019 Sep 21]. 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


Texas A&M University

8. Lee, Chun-I. C-H Borylation Mediated by Group 9 Pincer Complexes and Synthesis of Iridium Triflates and Triarylmethyl Species.

Degree: 2015, Texas A&M University

 The importance of organoboron compounds in chemical synthesis is apparent from the Nobel Prizes awarded to Herbert C. Brown (1979) and Akira Suzuki (2010) for… (more)

Subjects/Keywords: pincer complex; iridium; rhodium; borylation; alkyne; alkynylboronate; trityl

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APA (6th Edition):

Lee, C. (2015). C-H Borylation Mediated by Group 9 Pincer Complexes and Synthesis of Iridium Triflates and Triarylmethyl Species. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/161242

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, Chun-I. “C-H Borylation Mediated by Group 9 Pincer Complexes and Synthesis of Iridium Triflates and Triarylmethyl Species.” 2015. Thesis, Texas A&M University. Accessed September 21, 2019. http://hdl.handle.net/1969.1/161242.

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

MLA Handbook (7th Edition):

Lee, Chun-I. “C-H Borylation Mediated by Group 9 Pincer Complexes and Synthesis of Iridium Triflates and Triarylmethyl Species.” 2015. Web. 21 Sep 2019.

Vancouver:

Lee C. C-H Borylation Mediated by Group 9 Pincer Complexes and Synthesis of Iridium Triflates and Triarylmethyl Species. [Internet] [Thesis]. Texas A&M University; 2015. [cited 2019 Sep 21]. Available from: http://hdl.handle.net/1969.1/161242.

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. C-H Borylation Mediated by Group 9 Pincer Complexes and Synthesis of Iridium Triflates and Triarylmethyl Species. [Thesis]. Texas A&M University; 2015. Available from: http://hdl.handle.net/1969.1/161242

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


University of Illinois – Chicago

9. Mazzacano, Thomas J. New Developments in Base Metal-Catalyzed C-H Borylation.

Degree: 2017, University of Illinois – Chicago

 The catalytic functionalization of carbon-hydrogen bonds to form carbon-boron bonds is an emerging field in organometallic chemistry. Substrates containing carbon-boron bonds play a pivotal role… (more)

Subjects/Keywords: Base Metals Organometallic C-H Borylation Catalysis Catalyst

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APA (6th Edition):

Mazzacano, T. J. (2017). New Developments in Base Metal-Catalyzed C-H Borylation. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/22071

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):

Mazzacano, Thomas J. “New Developments in Base Metal-Catalyzed C-H Borylation.” 2017. Thesis, University of Illinois – Chicago. Accessed September 21, 2019. http://hdl.handle.net/10027/22071.

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

MLA Handbook (7th Edition):

Mazzacano, Thomas J. “New Developments in Base Metal-Catalyzed C-H Borylation.” 2017. Web. 21 Sep 2019.

Vancouver:

Mazzacano TJ. New Developments in Base Metal-Catalyzed C-H Borylation. [Internet] [Thesis]. University of Illinois – Chicago; 2017. [cited 2019 Sep 21]. Available from: http://hdl.handle.net/10027/22071.

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

Council of Science Editors:

Mazzacano TJ. New Developments in Base Metal-Catalyzed C-H Borylation. [Thesis]. University of Illinois – Chicago; 2017. Available from: http://hdl.handle.net/10027/22071

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


UCLA

10. Green, Aaron Gabriel. Computational Studies of Iridium-Catalyzed Borylation Reactions and Defying Torquoselectivity in Cyclobutene Ring-Opening via Strain-Induced Thermal Selectivity.

Degree: Chemistry, 2013, UCLA

 The studies reported in this dissertation illustrate a few selected examples of using density functional theory (DFT) calculations to investigate various aspects of iridium-catalyzed reactions… (more)

Subjects/Keywords: Chemistry; borylation; catalysis; computational chemistry; iridium; regioselectivity; torquoselectivity

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APA (6th Edition):

Green, A. G. (2013). Computational Studies of Iridium-Catalyzed Borylation Reactions and Defying Torquoselectivity in Cyclobutene Ring-Opening via Strain-Induced Thermal Selectivity. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/6fg683n9

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):

Green, Aaron Gabriel. “Computational Studies of Iridium-Catalyzed Borylation Reactions and Defying Torquoselectivity in Cyclobutene Ring-Opening via Strain-Induced Thermal Selectivity.” 2013. Thesis, UCLA. Accessed September 21, 2019. http://www.escholarship.org/uc/item/6fg683n9.

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

MLA Handbook (7th Edition):

Green, Aaron Gabriel. “Computational Studies of Iridium-Catalyzed Borylation Reactions and Defying Torquoselectivity in Cyclobutene Ring-Opening via Strain-Induced Thermal Selectivity.” 2013. Web. 21 Sep 2019.

Vancouver:

Green AG. Computational Studies of Iridium-Catalyzed Borylation Reactions and Defying Torquoselectivity in Cyclobutene Ring-Opening via Strain-Induced Thermal Selectivity. [Internet] [Thesis]. UCLA; 2013. [cited 2019 Sep 21]. Available from: http://www.escholarship.org/uc/item/6fg683n9.

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

Council of Science Editors:

Green AG. Computational Studies of Iridium-Catalyzed Borylation Reactions and Defying Torquoselectivity in Cyclobutene Ring-Opening via Strain-Induced Thermal Selectivity. [Thesis]. UCLA; 2013. Available from: http://www.escholarship.org/uc/item/6fg683n9

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


University of Manchester

11. Heard, Kane. Novel Polyaromatics for Organic Electronics and Graphene Exfoliation: Synthetic Approaches Utilising Regioselective Aromatic C-H Borylation.

Degree: 2016, University of Manchester

 Projects were undertaken investigating the functionalisation of polyaromatic cores (chrysene, pyrene and perylene) for use in organic electronics and aqueous graphene stabilisation. In each case… (more)

Subjects/Keywords: Polyaromatic Synthesis; C-H Borylation; Organic Electronics; Graphene Exfoliation

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APA (6th Edition):

Heard, K. (2016). Novel Polyaromatics for Organic Electronics and Graphene Exfoliation: Synthetic Approaches Utilising Regioselective Aromatic C-H Borylation. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301438

Chicago Manual of Style (16th Edition):

Heard, Kane. “Novel Polyaromatics for Organic Electronics and Graphene Exfoliation: Synthetic Approaches Utilising Regioselective Aromatic C-H Borylation.” 2016. Doctoral Dissertation, University of Manchester. Accessed September 21, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301438.

MLA Handbook (7th Edition):

Heard, Kane. “Novel Polyaromatics for Organic Electronics and Graphene Exfoliation: Synthetic Approaches Utilising Regioselective Aromatic C-H Borylation.” 2016. Web. 21 Sep 2019.

Vancouver:

Heard K. Novel Polyaromatics for Organic Electronics and Graphene Exfoliation: Synthetic Approaches Utilising Regioselective Aromatic C-H Borylation. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2019 Sep 21]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301438.

Council of Science Editors:

Heard K. Novel Polyaromatics for Organic Electronics and Graphene Exfoliation: Synthetic Approaches Utilising Regioselective Aromatic C-H Borylation. [Doctoral Dissertation]. University of Manchester; 2016. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301438


Virginia Tech

12. Nelson, Amanda Kay. Metal-Catalyzed Formation and Transformations of Carbon-Boron Bonds.

Degree: PhD, Chemistry, 2016, Virginia Tech

 Our research seeks new methods for functionalizing organic small molecules using organoboronic derivatives as a versatile handle for late-stage manipulations. Metal-catalyzed formation of new carbon-boron… (more)

Subjects/Keywords: borylation; diboration; conjugate addition; aqueous; copper; cross-coupling

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APA (6th Edition):

Nelson, A. K. (2016). Metal-Catalyzed Formation and Transformations of Carbon-Boron Bonds. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/83400

Chicago Manual of Style (16th Edition):

Nelson, Amanda Kay. “Metal-Catalyzed Formation and Transformations of Carbon-Boron Bonds.” 2016. Doctoral Dissertation, Virginia Tech. Accessed September 21, 2019. http://hdl.handle.net/10919/83400.

MLA Handbook (7th Edition):

Nelson, Amanda Kay. “Metal-Catalyzed Formation and Transformations of Carbon-Boron Bonds.” 2016. Web. 21 Sep 2019.

Vancouver:

Nelson AK. Metal-Catalyzed Formation and Transformations of Carbon-Boron Bonds. [Internet] [Doctoral dissertation]. Virginia Tech; 2016. [cited 2019 Sep 21]. Available from: http://hdl.handle.net/10919/83400.

Council of Science Editors:

Nelson AK. Metal-Catalyzed Formation and Transformations of Carbon-Boron Bonds. [Doctoral Dissertation]. Virginia Tech; 2016. Available from: http://hdl.handle.net/10919/83400


Virginia Tech

13. Sun, Jing. Synthesis and Application of Boronic Acid Derivatives.

Degree: MS, Chemistry, 2010, Virginia Tech

 Boronic acids are attractive synthetic intermediates and have been shown to be effective as inhibitors of various enzymes. In this project, the overarching goal is… (more)

Subjects/Keywords: ?-Borylation; Boronic Acid Derivatives; Human ClpXP; Pinacolyl Boronic Ester Deprotection

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APA (6th Edition):

Sun, J. (2010). Synthesis and Application of Boronic Acid Derivatives. (Masters Thesis). Virginia Tech. Retrieved from http://hdl.handle.net/10919/77006

Chicago Manual of Style (16th Edition):

Sun, Jing. “Synthesis and Application of Boronic Acid Derivatives.” 2010. Masters Thesis, Virginia Tech. Accessed September 21, 2019. http://hdl.handle.net/10919/77006.

MLA Handbook (7th Edition):

Sun, Jing. “Synthesis and Application of Boronic Acid Derivatives.” 2010. Web. 21 Sep 2019.

Vancouver:

Sun J. Synthesis and Application of Boronic Acid Derivatives. [Internet] [Masters thesis]. Virginia Tech; 2010. [cited 2019 Sep 21]. Available from: http://hdl.handle.net/10919/77006.

Council of Science Editors:

Sun J. Synthesis and Application of Boronic Acid Derivatives. [Masters Thesis]. Virginia Tech; 2010. Available from: http://hdl.handle.net/10919/77006


Virginia Tech

14. Thorpe, Steven Brandon. Activation of diboron reagents: The development of mild conditions for the synthesis of unique organoboron compounds.

Degree: PhD, Chemistry, 2012, Virginia Tech

 The first successful synthesis and isolation of a boronic acid was reported in 1860 by Frankland in the pursuit of novel organometallic compounds. For more… (more)

Subjects/Keywords: borylation; diboron reagent; boronic ester; conjugate addition; copper catalysis

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APA (6th Edition):

Thorpe, S. B. (2012). Activation of diboron reagents: The development of mild conditions for the synthesis of unique organoboron compounds. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/26669

Chicago Manual of Style (16th Edition):

Thorpe, Steven Brandon. “Activation of diboron reagents: The development of mild conditions for the synthesis of unique organoboron compounds.” 2012. Doctoral Dissertation, Virginia Tech. Accessed September 21, 2019. http://hdl.handle.net/10919/26669.

MLA Handbook (7th Edition):

Thorpe, Steven Brandon. “Activation of diboron reagents: The development of mild conditions for the synthesis of unique organoboron compounds.” 2012. Web. 21 Sep 2019.

Vancouver:

Thorpe SB. Activation of diboron reagents: The development of mild conditions for the synthesis of unique organoboron compounds. [Internet] [Doctoral dissertation]. Virginia Tech; 2012. [cited 2019 Sep 21]. Available from: http://hdl.handle.net/10919/26669.

Council of Science Editors:

Thorpe SB. Activation of diboron reagents: The development of mild conditions for the synthesis of unique organoboron compounds. [Doctoral Dissertation]. Virginia Tech; 2012. Available from: http://hdl.handle.net/10919/26669


Virginia Tech

15. Snead, Russell Franklin. Development of Novel, Regioselective Borylation Protocols.

Degree: PhD, Chemistry, 2018, Virginia Tech

 Organoboron compounds are highly valued synthetic intermediates due to their diverse array of reactivity, which is often utilized in the synthesis of valuable organic molecules.… (more)

Subjects/Keywords: borylation; transition metal-catalyzed; transition metal-free; allenes; alkynamides

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APA (6th Edition):

Snead, R. F. (2018). Development of Novel, Regioselective Borylation Protocols. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/85003

Chicago Manual of Style (16th Edition):

Snead, Russell Franklin. “Development of Novel, Regioselective Borylation Protocols.” 2018. Doctoral Dissertation, Virginia Tech. Accessed September 21, 2019. http://hdl.handle.net/10919/85003.

MLA Handbook (7th Edition):

Snead, Russell Franklin. “Development of Novel, Regioselective Borylation Protocols.” 2018. Web. 21 Sep 2019.

Vancouver:

Snead RF. Development of Novel, Regioselective Borylation Protocols. [Internet] [Doctoral dissertation]. Virginia Tech; 2018. [cited 2019 Sep 21]. Available from: http://hdl.handle.net/10919/85003.

Council of Science Editors:

Snead RF. Development of Novel, Regioselective Borylation Protocols. [Doctoral Dissertation]. Virginia Tech; 2018. Available from: http://hdl.handle.net/10919/85003


University of California – Irvine

16. Issaian, Adena. Carboxyboration: The Catalyst-Free Synthesis of Borylated Lactones and Isocoumarins From Esters.

Degree: Chemistry, 2016, University of California – Irvine

 Catalyst-free formation of isocoumarins and α-pyrones from the corresponding alkynyl esters is realized. The resulting γ- and δ-lactones are isolated as the pinacolboronic esters, boronic… (more)

Subjects/Keywords: Chemistry; borylation; catalyst-free; chlorocatecholborane; cyclization; electrophilic; oxyboration

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APA (6th Edition):

Issaian, A. (2016). Carboxyboration: The Catalyst-Free Synthesis of Borylated Lactones and Isocoumarins From Esters. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/0j63x4r0

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):

Issaian, Adena. “Carboxyboration: The Catalyst-Free Synthesis of Borylated Lactones and Isocoumarins From Esters.” 2016. Thesis, University of California – Irvine. Accessed September 21, 2019. http://www.escholarship.org/uc/item/0j63x4r0.

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

MLA Handbook (7th Edition):

Issaian, Adena. “Carboxyboration: The Catalyst-Free Synthesis of Borylated Lactones and Isocoumarins From Esters.” 2016. Web. 21 Sep 2019.

Vancouver:

Issaian A. Carboxyboration: The Catalyst-Free Synthesis of Borylated Lactones and Isocoumarins From Esters. [Internet] [Thesis]. University of California – Irvine; 2016. [cited 2019 Sep 21]. Available from: http://www.escholarship.org/uc/item/0j63x4r0.

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

Council of Science Editors:

Issaian A. Carboxyboration: The Catalyst-Free Synthesis of Borylated Lactones and Isocoumarins From Esters. [Thesis]. University of California – Irvine; 2016. Available from: http://www.escholarship.org/uc/item/0j63x4r0

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


Boston College

17. Eliseeva, Maria N. New Route to a [5,5] Carbon Nanotube End-Cap via Direct Borylation of Corannulene.

Degree: MS, Chemistry, 2011, Boston College

 The Scott lab is interested in the functionalization of corannulene as a building block for large polycyclic aromatic hydrocarbons and carbon nanotube end-cap precursors. Toward… (more)

Subjects/Keywords: carbon nanotube; corannulene; direct borylation; iridium catalyst; Suzuki reaction

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APA (6th Edition):

Eliseeva, M. N. (2011). New Route to a [5,5] Carbon Nanotube End-Cap via Direct Borylation of Corannulene. (Masters Thesis). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:101796

Chicago Manual of Style (16th Edition):

Eliseeva, Maria N. “New Route to a [5,5] Carbon Nanotube End-Cap via Direct Borylation of Corannulene.” 2011. Masters Thesis, Boston College. Accessed September 21, 2019. http://dlib.bc.edu/islandora/object/bc-ir:101796.

MLA Handbook (7th Edition):

Eliseeva, Maria N. “New Route to a [5,5] Carbon Nanotube End-Cap via Direct Borylation of Corannulene.” 2011. Web. 21 Sep 2019.

Vancouver:

Eliseeva MN. New Route to a [5,5] Carbon Nanotube End-Cap via Direct Borylation of Corannulene. [Internet] [Masters thesis]. Boston College; 2011. [cited 2019 Sep 21]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101796.

Council of Science Editors:

Eliseeva MN. New Route to a [5,5] Carbon Nanotube End-Cap via Direct Borylation of Corannulene. [Masters Thesis]. Boston College; 2011. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101796


University of Manchester

18. Heard, Kane. Novel polyaromatics for organic electronics and graphene exfoliation : synthetic approaches utilising regioselective aromatic C-H borylation.

Degree: PhD, 2016, University of Manchester

 Projects were undertaken investigating the functionalisation of polyaromatic cores (chrysene, pyrene and perylene) for use in organic electronics and aqueous graphene stabilisation. In each case… (more)

Subjects/Keywords: 547; Polyaromatic Synthesis; C-H Borylation; Organic Electronics; Graphene Exfoliation

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APA (6th Edition):

Heard, K. (2016). Novel polyaromatics for organic electronics and graphene exfoliation : synthetic approaches utilising regioselective aromatic C-H borylation. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/novel-polyaromatics-for-organic-electronics-and-graphene-exfoliation-synthetic-approaches-utilising-regioselective-aromatic-ch-borylation(f8cd1879-521e-41f6-8a3c-2af7add7844b).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.727929

Chicago Manual of Style (16th Edition):

Heard, Kane. “Novel polyaromatics for organic electronics and graphene exfoliation : synthetic approaches utilising regioselective aromatic C-H borylation.” 2016. Doctoral Dissertation, University of Manchester. Accessed September 21, 2019. https://www.research.manchester.ac.uk/portal/en/theses/novel-polyaromatics-for-organic-electronics-and-graphene-exfoliation-synthetic-approaches-utilising-regioselective-aromatic-ch-borylation(f8cd1879-521e-41f6-8a3c-2af7add7844b).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.727929.

MLA Handbook (7th Edition):

Heard, Kane. “Novel polyaromatics for organic electronics and graphene exfoliation : synthetic approaches utilising regioselective aromatic C-H borylation.” 2016. Web. 21 Sep 2019.

Vancouver:

Heard K. Novel polyaromatics for organic electronics and graphene exfoliation : synthetic approaches utilising regioselective aromatic C-H borylation. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2019 Sep 21]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/novel-polyaromatics-for-organic-electronics-and-graphene-exfoliation-synthetic-approaches-utilising-regioselective-aromatic-ch-borylation(f8cd1879-521e-41f6-8a3c-2af7add7844b).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.727929.

Council of Science Editors:

Heard K. Novel polyaromatics for organic electronics and graphene exfoliation : synthetic approaches utilising regioselective aromatic C-H borylation. [Doctoral Dissertation]. University of Manchester; 2016. Available from: https://www.research.manchester.ac.uk/portal/en/theses/novel-polyaromatics-for-organic-electronics-and-graphene-exfoliation-synthetic-approaches-utilising-regioselective-aromatic-ch-borylation(f8cd1879-521e-41f6-8a3c-2af7add7844b).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.727929

19. Del Grosso, Alessandro. Borenium Cations for the Direct Electrophilic Borylation of Arenes.

Degree: 2013, University of Manchester

A catalytic (in Brønsted superacid) and a stoichiometric process were developed to synthesise aryl boronic esters with boron cations via electrophilic arene borylation. The treatment… (more)

Subjects/Keywords: borenium; borocation; borylation; boronic ester; boronate ester; electrophilic borylation

…222 9 Abstract Borenium Cations for the Direct Electrophilic Borylation of Arenes… …borylation. The treatment of CatBX (Cat = catecholate; X = Cl, Br) with the triethyl salt… …electrophilic aromatic borylation at 25 °C. The by-product of the reaction was a strong Brønsted acid… …that was able to catalyse arene borylation using CatBH at high temperature. This catalytic… …regioselective borylation, by electrophilic aromatic substitution, of a range of N-heterocycles… 

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APA (6th Edition):

Del Grosso, A. (2013). Borenium Cations for the Direct Electrophilic Borylation of Arenes. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:189470

Chicago Manual of Style (16th Edition):

Del Grosso, Alessandro. “Borenium Cations for the Direct Electrophilic Borylation of Arenes.” 2013. Doctoral Dissertation, University of Manchester. Accessed September 21, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:189470.

MLA Handbook (7th Edition):

Del Grosso, Alessandro. “Borenium Cations for the Direct Electrophilic Borylation of Arenes.” 2013. Web. 21 Sep 2019.

Vancouver:

Del Grosso A. Borenium Cations for the Direct Electrophilic Borylation of Arenes. [Internet] [Doctoral dissertation]. University of Manchester; 2013. [cited 2019 Sep 21]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:189470.

Council of Science Editors:

Del Grosso A. Borenium Cations for the Direct Electrophilic Borylation of Arenes. [Doctoral Dissertation]. University of Manchester; 2013. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:189470

20. Bheeter, Linus Paulin. catalyseurs à base de ligands carbène N-hétérocycliques dérivés de fer et de nickel pour les réactions catalytiques d'hydrosilylation et d'hydroboration : Iron and Nickel N-heterocyclic carbenes complexes for catalyzed hydrosilylation and borylation reactions.

Degree: Docteur es, Chimie, 2014, Rennes 1

Ces travaux de thèse portent sur le développement de catalyseurs à base de ligands carbène N-hétérocycliques dérivés de fer et de nickel, deux métaux de… (more)

Subjects/Keywords: Nickel; Fer; Ligands carbènes N-Hétérocycliques; Hydrosilylation; Borylation; Aldéhydes; Cétones; Imines; Nickel; Iron; N-Heterocyclic carbene ligands; Hydrosilylation; Borylation; Aldehydes; Ketones; Imines

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APA (6th Edition):

Bheeter, L. P. (2014). catalyseurs à base de ligands carbène N-hétérocycliques dérivés de fer et de nickel pour les réactions catalytiques d'hydrosilylation et d'hydroboration : Iron and Nickel N-heterocyclic carbenes complexes for catalyzed hydrosilylation and borylation reactions. (Doctoral Dissertation). Rennes 1. Retrieved from http://www.theses.fr/2014REN1S182

Chicago Manual of Style (16th Edition):

Bheeter, Linus Paulin. “catalyseurs à base de ligands carbène N-hétérocycliques dérivés de fer et de nickel pour les réactions catalytiques d'hydrosilylation et d'hydroboration : Iron and Nickel N-heterocyclic carbenes complexes for catalyzed hydrosilylation and borylation reactions.” 2014. Doctoral Dissertation, Rennes 1. Accessed September 21, 2019. http://www.theses.fr/2014REN1S182.

MLA Handbook (7th Edition):

Bheeter, Linus Paulin. “catalyseurs à base de ligands carbène N-hétérocycliques dérivés de fer et de nickel pour les réactions catalytiques d'hydrosilylation et d'hydroboration : Iron and Nickel N-heterocyclic carbenes complexes for catalyzed hydrosilylation and borylation reactions.” 2014. Web. 21 Sep 2019.

Vancouver:

Bheeter LP. catalyseurs à base de ligands carbène N-hétérocycliques dérivés de fer et de nickel pour les réactions catalytiques d'hydrosilylation et d'hydroboration : Iron and Nickel N-heterocyclic carbenes complexes for catalyzed hydrosilylation and borylation reactions. [Internet] [Doctoral dissertation]. Rennes 1; 2014. [cited 2019 Sep 21]. Available from: http://www.theses.fr/2014REN1S182.

Council of Science Editors:

Bheeter LP. catalyseurs à base de ligands carbène N-hétérocycliques dérivés de fer et de nickel pour les réactions catalytiques d'hydrosilylation et d'hydroboration : Iron and Nickel N-heterocyclic carbenes complexes for catalyzed hydrosilylation and borylation reactions. [Doctoral Dissertation]. Rennes 1; 2014. Available from: http://www.theses.fr/2014REN1S182

21. Charbonnier, Jean-Baptiste. Réaction de nitration en continu pour la synthèse d’un principe actif pharmaceutique : fonctionnalisation d’hétérocycles borés obtenus par borylation électrophile : Continuous nitration reaction for the synthesis of an active pharmaceutical ingredient : functionnalisation of boron heterocycles synthetised by electrophilic borylation.

Degree: Docteur es, Chimie organique, 2018, Bordeaux

La fluidique est un outil offrant des avantages industriels notamment en termes de sécurité grâce à un meilleur contrôle thermique mais aussi une diminution des… (more)

Subjects/Keywords: Microfluidique; Principe actif pharmaceutique; Nitration d'alcool; Micromélangeur; Borylation électrophile; Oxaborinine; Complexe amine-borane; Microfluidic; Active pharmaceutical ingredient; Alcohol nitration; Micromixer; Electrophilic borylation; Oxaborinin; Amine-borane complex

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APA (6th Edition):

Charbonnier, J. (2018). Réaction de nitration en continu pour la synthèse d’un principe actif pharmaceutique : fonctionnalisation d’hétérocycles borés obtenus par borylation électrophile : Continuous nitration reaction for the synthesis of an active pharmaceutical ingredient : functionnalisation of boron heterocycles synthetised by electrophilic borylation. (Doctoral Dissertation). Bordeaux. Retrieved from http://www.theses.fr/2018BORD0078

Chicago Manual of Style (16th Edition):

Charbonnier, Jean-Baptiste. “Réaction de nitration en continu pour la synthèse d’un principe actif pharmaceutique : fonctionnalisation d’hétérocycles borés obtenus par borylation électrophile : Continuous nitration reaction for the synthesis of an active pharmaceutical ingredient : functionnalisation of boron heterocycles synthetised by electrophilic borylation.” 2018. Doctoral Dissertation, Bordeaux. Accessed September 21, 2019. http://www.theses.fr/2018BORD0078.

MLA Handbook (7th Edition):

Charbonnier, Jean-Baptiste. “Réaction de nitration en continu pour la synthèse d’un principe actif pharmaceutique : fonctionnalisation d’hétérocycles borés obtenus par borylation électrophile : Continuous nitration reaction for the synthesis of an active pharmaceutical ingredient : functionnalisation of boron heterocycles synthetised by electrophilic borylation.” 2018. Web. 21 Sep 2019.

Vancouver:

Charbonnier J. Réaction de nitration en continu pour la synthèse d’un principe actif pharmaceutique : fonctionnalisation d’hétérocycles borés obtenus par borylation électrophile : Continuous nitration reaction for the synthesis of an active pharmaceutical ingredient : functionnalisation of boron heterocycles synthetised by electrophilic borylation. [Internet] [Doctoral dissertation]. Bordeaux; 2018. [cited 2019 Sep 21]. Available from: http://www.theses.fr/2018BORD0078.

Council of Science Editors:

Charbonnier J. Réaction de nitration en continu pour la synthèse d’un principe actif pharmaceutique : fonctionnalisation d’hétérocycles borés obtenus par borylation électrophile : Continuous nitration reaction for the synthesis of an active pharmaceutical ingredient : functionnalisation of boron heterocycles synthetised by electrophilic borylation. [Doctoral Dissertation]. Bordeaux; 2018. Available from: http://www.theses.fr/2018BORD0078

22. Martin, Thibaut. Etude de nouvelles méthodologies d'hétéroarylation directe de liaison C-Het C-Br en série thiazolique : application à la synthèse de coeurs thiazolylpyridiniques des thiopeptides de la série d : Development of new-pallado-catalyzed direct arylation methodologies in the thiazole serie : application to the synthesis of serie d thiopeptide antibiotics cores.

Degree: Docteur es, Chimie, 2010, Rouen, INSA

Face à l’apparition alarmante et continue de résistance massive des bactéries à l’arsenal actuel d’antibiotiques, la recherche de nouveaux agents antibactériens est actuellement un enjeu… (more)

Subjects/Keywords: Thiazole; Hétérocycles; Thiopeptides antibiotiques; Arylation directe; Borylation; Couplage de Suzuki; Heterocycles; Thiopeptide family; Suzuki coupling

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APA (6th Edition):

Martin, T. (2010). Etude de nouvelles méthodologies d'hétéroarylation directe de liaison C-Het C-Br en série thiazolique : application à la synthèse de coeurs thiazolylpyridiniques des thiopeptides de la série d : Development of new-pallado-catalyzed direct arylation methodologies in the thiazole serie : application to the synthesis of serie d thiopeptide antibiotics cores. (Doctoral Dissertation). Rouen, INSA. Retrieved from http://www.theses.fr/2010ISAM0004

Chicago Manual of Style (16th Edition):

Martin, Thibaut. “Etude de nouvelles méthodologies d'hétéroarylation directe de liaison C-Het C-Br en série thiazolique : application à la synthèse de coeurs thiazolylpyridiniques des thiopeptides de la série d : Development of new-pallado-catalyzed direct arylation methodologies in the thiazole serie : application to the synthesis of serie d thiopeptide antibiotics cores.” 2010. Doctoral Dissertation, Rouen, INSA. Accessed September 21, 2019. http://www.theses.fr/2010ISAM0004.

MLA Handbook (7th Edition):

Martin, Thibaut. “Etude de nouvelles méthodologies d'hétéroarylation directe de liaison C-Het C-Br en série thiazolique : application à la synthèse de coeurs thiazolylpyridiniques des thiopeptides de la série d : Development of new-pallado-catalyzed direct arylation methodologies in the thiazole serie : application to the synthesis of serie d thiopeptide antibiotics cores.” 2010. Web. 21 Sep 2019.

Vancouver:

Martin T. Etude de nouvelles méthodologies d'hétéroarylation directe de liaison C-Het C-Br en série thiazolique : application à la synthèse de coeurs thiazolylpyridiniques des thiopeptides de la série d : Development of new-pallado-catalyzed direct arylation methodologies in the thiazole serie : application to the synthesis of serie d thiopeptide antibiotics cores. [Internet] [Doctoral dissertation]. Rouen, INSA; 2010. [cited 2019 Sep 21]. Available from: http://www.theses.fr/2010ISAM0004.

Council of Science Editors:

Martin T. Etude de nouvelles méthodologies d'hétéroarylation directe de liaison C-Het C-Br en série thiazolique : application à la synthèse de coeurs thiazolylpyridiniques des thiopeptides de la série d : Development of new-pallado-catalyzed direct arylation methodologies in the thiazole serie : application to the synthesis of serie d thiopeptide antibiotics cores. [Doctoral Dissertation]. Rouen, INSA; 2010. Available from: http://www.theses.fr/2010ISAM0004


University of Manchester

23. Ayuso Carrillo, Josue Israel. Low cost, more efficient, and less toxic synthetic routes to conjugated polymers.

Degree: 2016, University of Manchester

 As key components of flexible organic electronics, the synthesis ofpolythiophenes via less toxic and more cost-effective routes is demanded. Anefficient synthetic route for the production… (more)

Subjects/Keywords: conjugated polymers; Suzuki-Miyaura cross-coupling; Electrophilic borylation; MIDA boronates; slow release; thiophenes; organic electronics

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APA (6th Edition):

Ayuso Carrillo, J. I. (2016). Low cost, more efficient, and less toxic synthetic routes to conjugated polymers. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:302874

Chicago Manual of Style (16th Edition):

Ayuso Carrillo, Josue Israel. “Low cost, more efficient, and less toxic synthetic routes to conjugated polymers.” 2016. Doctoral Dissertation, University of Manchester. Accessed September 21, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:302874.

MLA Handbook (7th Edition):

Ayuso Carrillo, Josue Israel. “Low cost, more efficient, and less toxic synthetic routes to conjugated polymers.” 2016. Web. 21 Sep 2019.

Vancouver:

Ayuso Carrillo JI. Low cost, more efficient, and less toxic synthetic routes to conjugated polymers. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2019 Sep 21]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:302874.

Council of Science Editors:

Ayuso Carrillo JI. Low cost, more efficient, and less toxic synthetic routes to conjugated polymers. [Doctoral Dissertation]. University of Manchester; 2016. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:302874


Universitat Rovira i Virgili

24. Palau Lluch, Gerard. alpha,beta-difunctionalization of alpha,beta-unsaturated carbonyl compounds through borylation reaction.

Degree: Departament de Química Física i Inorgànica, 2015, Universitat Rovira i Virgili

 This thesis presents the results concerning new methodologies towards the obtantion of alpha-functionalized beta-borylated compounds from alpha,beta-unsaturated carbonyl compounds, with no precedent in the litherature.… (more)

Subjects/Keywords: Borilació; Halogenació; Difuncionalització; Borilación; Halogenación; Difuncionalización; Borylation; Halogenation; Difunctionalization; 54; 546; 547; 6

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APA (6th Edition):

Palau Lluch, G. (2015). alpha,beta-difunctionalization of alpha,beta-unsaturated carbonyl compounds through borylation reaction. (Thesis). Universitat Rovira i Virgili. Retrieved from http://hdl.handle.net/10803/311620

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):

Palau Lluch, Gerard. “alpha,beta-difunctionalization of alpha,beta-unsaturated carbonyl compounds through borylation reaction.” 2015. Thesis, Universitat Rovira i Virgili. Accessed September 21, 2019. http://hdl.handle.net/10803/311620.

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

MLA Handbook (7th Edition):

Palau Lluch, Gerard. “alpha,beta-difunctionalization of alpha,beta-unsaturated carbonyl compounds through borylation reaction.” 2015. Web. 21 Sep 2019.

Vancouver:

Palau Lluch G. alpha,beta-difunctionalization of alpha,beta-unsaturated carbonyl compounds through borylation reaction. [Internet] [Thesis]. Universitat Rovira i Virgili; 2015. [cited 2019 Sep 21]. Available from: http://hdl.handle.net/10803/311620.

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

Council of Science Editors:

Palau Lluch G. alpha,beta-difunctionalization of alpha,beta-unsaturated carbonyl compounds through borylation reaction. [Thesis]. Universitat Rovira i Virgili; 2015. Available from: http://hdl.handle.net/10803/311620

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


Texas A&M University

25. Press, Loren Paul. High-Turnover C-H Borylation of Arenes with (POCOP) Iridium Complexes, The Synthesis of Group 9/10 (POCS) Complexes and the Study of Triflyloxy-Substituted Carboranes.

Degree: PhD, Chemistry, 2016, Texas A&M University

 Over the last century, transition metal-catalyzed C-H functionalization has emerged as one of the most important topics in synthetic chemistry. One type of C-H functionalization,… (more)

Subjects/Keywords: C-H functionalization; C-H activation; borylation; POCOP; iridium; POCS; triflyloxy; carboranes; weakly coordinating anions

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APA (6th Edition):

Press, L. P. (2016). High-Turnover C-H Borylation of Arenes with (POCOP) Iridium Complexes, The Synthesis of Group 9/10 (POCS) Complexes and the Study of Triflyloxy-Substituted Carboranes. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/158080

Chicago Manual of Style (16th Edition):

Press, Loren Paul. “High-Turnover C-H Borylation of Arenes with (POCOP) Iridium Complexes, The Synthesis of Group 9/10 (POCS) Complexes and the Study of Triflyloxy-Substituted Carboranes.” 2016. Doctoral Dissertation, Texas A&M University. Accessed September 21, 2019. http://hdl.handle.net/1969.1/158080.

MLA Handbook (7th Edition):

Press, Loren Paul. “High-Turnover C-H Borylation of Arenes with (POCOP) Iridium Complexes, The Synthesis of Group 9/10 (POCS) Complexes and the Study of Triflyloxy-Substituted Carboranes.” 2016. Web. 21 Sep 2019.

Vancouver:

Press LP. High-Turnover C-H Borylation of Arenes with (POCOP) Iridium Complexes, The Synthesis of Group 9/10 (POCS) Complexes and the Study of Triflyloxy-Substituted Carboranes. [Internet] [Doctoral dissertation]. Texas A&M University; 2016. [cited 2019 Sep 21]. Available from: http://hdl.handle.net/1969.1/158080.

Council of Science Editors:

Press LP. High-Turnover C-H Borylation of Arenes with (POCOP) Iridium Complexes, The Synthesis of Group 9/10 (POCS) Complexes and the Study of Triflyloxy-Substituted Carboranes. [Doctoral Dissertation]. Texas A&M University; 2016. Available from: http://hdl.handle.net/1969.1/158080

26. Zhang, Na. Nickel Catalyzed Borylation and Cross-Coupling of Representative C-O Based Electrophiles.

Degree: 2015, University of Pennsylvania

 The Suzuki-Miyaura cross-coupling is widely used in the synthesis of pharmaceuticals, agrochemicals, and organic light-emitting materials. Utilization of phenol derivatives in Suzuki-Miyaura coupling is economically,… (more)

Subjects/Keywords: Borylation; C-O Electrophile; Cross-Coupling; Nickel; Suzuki-Miyaura; Chemistry; Inorganic Chemistry; Organic Chemistry

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APA (6th Edition):

Zhang, N. (2015). Nickel Catalyzed Borylation and Cross-Coupling of Representative C-O Based Electrophiles. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/1170

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):

Zhang, Na. “Nickel Catalyzed Borylation and Cross-Coupling of Representative C-O Based Electrophiles.” 2015. Thesis, University of Pennsylvania. Accessed September 21, 2019. https://repository.upenn.edu/edissertations/1170.

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

MLA Handbook (7th Edition):

Zhang, Na. “Nickel Catalyzed Borylation and Cross-Coupling of Representative C-O Based Electrophiles.” 2015. Web. 21 Sep 2019.

Vancouver:

Zhang N. Nickel Catalyzed Borylation and Cross-Coupling of Representative C-O Based Electrophiles. [Internet] [Thesis]. University of Pennsylvania; 2015. [cited 2019 Sep 21]. Available from: https://repository.upenn.edu/edissertations/1170.

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

Council of Science Editors:

Zhang N. Nickel Catalyzed Borylation and Cross-Coupling of Representative C-O Based Electrophiles. [Thesis]. University of Pennsylvania; 2015. Available from: https://repository.upenn.edu/edissertations/1170

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


Queens University

27. Cosman, Jennifer. Advances in Metal-Catalyzed C–H Borylation and Multicomponent Allylic Substitution Reactions .

Degree: Chemistry, 2015, Queens University

 Chapter one of this thesis describes the iridium-catalyzed ortho-selective C–H borylation reaction of tertiary benzamides. An iridium(I) complex paired with an electron-deficient phosphine ligand allows… (more)

Subjects/Keywords: multicomponent reactions; C-H activation; allylic substitution; Mizoroki-Heck reaction; iridium-catalyzed C-H borylation

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APA (6th Edition):

Cosman, J. (2015). Advances in Metal-Catalyzed C–H Borylation and Multicomponent Allylic Substitution Reactions . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/13534

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):

Cosman, Jennifer. “Advances in Metal-Catalyzed C–H Borylation and Multicomponent Allylic Substitution Reactions .” 2015. Thesis, Queens University. Accessed September 21, 2019. http://hdl.handle.net/1974/13534.

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

MLA Handbook (7th Edition):

Cosman, Jennifer. “Advances in Metal-Catalyzed C–H Borylation and Multicomponent Allylic Substitution Reactions .” 2015. Web. 21 Sep 2019.

Vancouver:

Cosman J. Advances in Metal-Catalyzed C–H Borylation and Multicomponent Allylic Substitution Reactions . [Internet] [Thesis]. Queens University; 2015. [cited 2019 Sep 21]. Available from: http://hdl.handle.net/1974/13534.

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

Council of Science Editors:

Cosman J. Advances in Metal-Catalyzed C–H Borylation and Multicomponent Allylic Substitution Reactions . [Thesis]. Queens University; 2015. Available from: http://hdl.handle.net/1974/13534

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

28. Liskey, Carl. Iridium-catalyzed borylation of aromatic and aliphatic C-H bonds: methodology and mechanism.

Degree: PhD, 0335, 2013, University of Illinois – Urbana-Champaign

 A method to conduct the one-pot, meta cyanation of arenes by iridium-catalyzed C-H borylation and copper-mediated cyanation of the resulting arylboronate esters is described in… (more)

Subjects/Keywords: borylation; C-H borylation; C-H activation; iridium; iridium-catalyzed borylation

…FG R, R' = EDG EAS C-H functionalization R R' 1. Borylation 2… …reactions. Then a more thorough background on C-H borylation reactions, the topic of this thesis… …approach has been used in arene functionalization for the ortho-borylation of phenols,61… …silylation of benzyl alcohols,62 and C-H borylation of indoles at the 7-position of the indole ring… …63 Sawamura and co-workers reported another example of directed C-H borylation with a… 

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

APA (6th Edition):

Liskey, C. (2013). Iridium-catalyzed borylation of aromatic and aliphatic C-H bonds: methodology and mechanism. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/45525

Chicago Manual of Style (16th Edition):

Liskey, Carl. “Iridium-catalyzed borylation of aromatic and aliphatic C-H bonds: methodology and mechanism.” 2013. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 21, 2019. http://hdl.handle.net/2142/45525.

MLA Handbook (7th Edition):

Liskey, Carl. “Iridium-catalyzed borylation of aromatic and aliphatic C-H bonds: methodology and mechanism.” 2013. Web. 21 Sep 2019.

Vancouver:

Liskey C. Iridium-catalyzed borylation of aromatic and aliphatic C-H bonds: methodology and mechanism. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2013. [cited 2019 Sep 21]. Available from: http://hdl.handle.net/2142/45525.

Council of Science Editors:

Liskey C. Iridium-catalyzed borylation of aromatic and aliphatic C-H bonds: methodology and mechanism. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2013. Available from: http://hdl.handle.net/2142/45525

29. Audi, Hassib. Synthèse stéréosélective d'aminoacides boronatés et silylés pour le piégeage de fluorures, à visée imagerie médicale : Stereoselective synthesis of boronated and silylated amino acids for fluorine trapping, referred to medical imaging.

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

La synthèse stéréosélective d'une nouvelle classe d'amino acides boronatés est réalisée par réaction de Wittig, puis borylation catalysée par un complexe d'iridium. Des amino esters… (more)

Subjects/Keywords: Acides aminés; Réaction de Wittig; Boronation; Fluoration; Iodation; Trifluoroborates; Amino acids; Wittig reaction; Borylation; Iridium catalysis; Iodation; Trifluoroborates; 541.39; 547; 572.8

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

APA (6th Edition):

Audi, H. (2012). Synthèse stéréosélective d'aminoacides boronatés et silylés pour le piégeage de fluorures, à visée imagerie médicale : Stereoselective synthesis of boronated and silylated amino acids for fluorine trapping, referred to medical imaging. (Doctoral Dissertation). Université de Bourgogne. Retrieved from http://www.theses.fr/2012DIJOS094

Chicago Manual of Style (16th Edition):

Audi, Hassib. “Synthèse stéréosélective d'aminoacides boronatés et silylés pour le piégeage de fluorures, à visée imagerie médicale : Stereoselective synthesis of boronated and silylated amino acids for fluorine trapping, referred to medical imaging.” 2012. Doctoral Dissertation, Université de Bourgogne. Accessed September 21, 2019. http://www.theses.fr/2012DIJOS094.

MLA Handbook (7th Edition):

Audi, Hassib. “Synthèse stéréosélective d'aminoacides boronatés et silylés pour le piégeage de fluorures, à visée imagerie médicale : Stereoselective synthesis of boronated and silylated amino acids for fluorine trapping, referred to medical imaging.” 2012. Web. 21 Sep 2019.

Vancouver:

Audi H. Synthèse stéréosélective d'aminoacides boronatés et silylés pour le piégeage de fluorures, à visée imagerie médicale : Stereoselective synthesis of boronated and silylated amino acids for fluorine trapping, referred to medical imaging. [Internet] [Doctoral dissertation]. Université de Bourgogne; 2012. [cited 2019 Sep 21]. Available from: http://www.theses.fr/2012DIJOS094.

Council of Science Editors:

Audi H. Synthèse stéréosélective d'aminoacides boronatés et silylés pour le piégeage de fluorures, à visée imagerie médicale : Stereoselective synthesis of boronated and silylated amino acids for fluorine trapping, referred to medical imaging. [Doctoral Dissertation]. Université de Bourgogne; 2012. Available from: http://www.theses.fr/2012DIJOS094


Kyoto University / 京都大学

30. Semba, Kazuhiko. Highly Efficient Catalytic Transformations of Unsaturated Compounds via Ligand-Induced Selective Addition of Copper Species : 銅化学種の配位子制御による選択的付加を鍵とする不飽和化合物の触媒的高効率分子変換反応.

Degree: 博士(工学), 2013, Kyoto University / 京都大学

新制・課程博士

甲第17522号

工博第3681号

Subjects/Keywords: copper; homogeneous catalyst; unsaturated compounds; ligand; borylation; reduction

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

APA (6th Edition):

Semba, K. (2013). Highly Efficient Catalytic Transformations of Unsaturated Compounds via Ligand-Induced Selective Addition of Copper Species : 銅化学種の配位子制御による選択的付加を鍵とする不飽和化合物の触媒的高効率分子変換反応. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/174888 ; http://dx.doi.org/10.14989/doctor.k17522

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):

Semba, Kazuhiko. “Highly Efficient Catalytic Transformations of Unsaturated Compounds via Ligand-Induced Selective Addition of Copper Species : 銅化学種の配位子制御による選択的付加を鍵とする不飽和化合物の触媒的高効率分子変換反応.” 2013. Thesis, Kyoto University / 京都大学. Accessed September 21, 2019. http://hdl.handle.net/2433/174888 ; http://dx.doi.org/10.14989/doctor.k17522.

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

MLA Handbook (7th Edition):

Semba, Kazuhiko. “Highly Efficient Catalytic Transformations of Unsaturated Compounds via Ligand-Induced Selective Addition of Copper Species : 銅化学種の配位子制御による選択的付加を鍵とする不飽和化合物の触媒的高効率分子変換反応.” 2013. Web. 21 Sep 2019.

Vancouver:

Semba K. Highly Efficient Catalytic Transformations of Unsaturated Compounds via Ligand-Induced Selective Addition of Copper Species : 銅化学種の配位子制御による選択的付加を鍵とする不飽和化合物の触媒的高効率分子変換反応. [Internet] [Thesis]. Kyoto University / 京都大学; 2013. [cited 2019 Sep 21]. Available from: http://hdl.handle.net/2433/174888 ; http://dx.doi.org/10.14989/doctor.k17522.

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

Council of Science Editors:

Semba K. Highly Efficient Catalytic Transformations of Unsaturated Compounds via Ligand-Induced Selective Addition of Copper Species : 銅化学種の配位子制御による選択的付加を鍵とする不飽和化合物の触媒的高効率分子変換反応. [Thesis]. Kyoto University / 京都大学; 2013. Available from: http://hdl.handle.net/2433/174888 ; http://dx.doi.org/10.14989/doctor.k17522

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

[1] [2]

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