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You searched for subject:(borylation). Showing records 1 – 30 of 36 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 October 22, 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. 22 Oct 2019.

Vancouver:

Cavalcanti L. Potassium Organotrifluoroborates: Chemistry Beyond Cross-Coupling. [Internet] [Thesis]. University of Pennsylvania; 2013. [cited 2019 Oct 22]. 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 October 22, 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. 22 Oct 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 Oct 22]. 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 Alberta

3. 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 October 22, 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. 22 Oct 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 Oct 22]. 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

4. 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 October 22, 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. 22 Oct 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 Oct 22]. 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

5. 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 October 22, 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. 22 Oct 2019.

Vancouver:

Romero EA. Taming Carbene Copper(I)-Hydride Complexes. [Internet] [Thesis]. University of California – San Diego; 2019. [cited 2019 Oct 22]. 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

6. 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


Texas A&M University

7. 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 October 22, 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. 22 Oct 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 Oct 22]. 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


UCLA

8. 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 October 22, 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. 22 Oct 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 Oct 22]. 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

9. 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 October 22, 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. 22 Oct 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 Oct 22]. 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

10. 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 October 22, 2019. http://hdl.handle.net/10919/77006.

MLA Handbook (7th Edition):

Sun, Jing. “Synthesis and Application of Boronic Acid Derivatives.” 2010. Web. 22 Oct 2019.

Vancouver:

Sun J. Synthesis and Application of Boronic Acid Derivatives. [Internet] [Masters thesis]. Virginia Tech; 2010. [cited 2019 Oct 22]. 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


University of California – Irvine

11. 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 October 22, 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. 22 Oct 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 Oct 22]. 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

12. 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 October 22, 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. 22 Oct 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 Oct 22]. 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

13. 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 October 22, 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. 22 Oct 2019.

Vancouver:

Del Grosso A. Borenium Cations for the Direct Electrophilic Borylation of Arenes. [Internet] [Doctoral dissertation]. University of Manchester; 2013. [cited 2019 Oct 22]. 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

14. 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 October 22, 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. 22 Oct 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 Oct 22]. 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


University of Manchester

15. 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 October 22, 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. 22 Oct 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 Oct 22]. 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


Texas A&M University

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

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 October 22, 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. 22 Oct 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 Oct 22]. 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

17. 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 October 22, 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. 22 Oct 2019.

Vancouver:

Zhang N. Nickel Catalyzed Borylation and Cross-Coupling of Representative C-O Based Electrophiles. [Internet] [Thesis]. University of Pennsylvania; 2015. [cited 2019 Oct 22]. 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

18. 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 October 22, 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. 22 Oct 2019.

Vancouver:

Cosman J. Advances in Metal-Catalyzed C–H Borylation and Multicomponent Allylic Substitution Reactions . [Internet] [Thesis]. Queens University; 2015. [cited 2019 Oct 22]. 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

19. 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 (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 October 22, 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. 22 Oct 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 Oct 22]. 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


Kyoto University / 京都大学

20. 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 (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 October 22, 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. 22 Oct 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 Oct 22]. 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


Kyoto University / 京都大学

21. Morimoto, Masao. Development of Highly Efficient Synthetic Reactions Catalyzed by Transition Metals : 遷移金属触媒を用いる高効率な合成反応の開発.

Degree: 博士(工学), 2014, Kyoto University / 京都大学

新制・課程博士

甲第18300号

工博第3892号

Subjects/Keywords: transition metal catalyst; metalacycle; cycloaddition; borylation; amination

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APA (6th Edition):

Morimoto, M. (2014). Development of Highly Efficient Synthetic Reactions Catalyzed by Transition Metals : 遷移金属触媒を用いる高効率な合成反応の開発. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/188615 ; http://dx.doi.org/10.14989/doctor.k18300

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):

Morimoto, Masao. “Development of Highly Efficient Synthetic Reactions Catalyzed by Transition Metals : 遷移金属触媒を用いる高効率な合成反応の開発.” 2014. Thesis, Kyoto University / 京都大学. Accessed October 22, 2019. http://hdl.handle.net/2433/188615 ; http://dx.doi.org/10.14989/doctor.k18300.

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

MLA Handbook (7th Edition):

Morimoto, Masao. “Development of Highly Efficient Synthetic Reactions Catalyzed by Transition Metals : 遷移金属触媒を用いる高効率な合成反応の開発.” 2014. Web. 22 Oct 2019.

Vancouver:

Morimoto M. Development of Highly Efficient Synthetic Reactions Catalyzed by Transition Metals : 遷移金属触媒を用いる高効率な合成反応の開発. [Internet] [Thesis]. Kyoto University / 京都大学; 2014. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/2433/188615 ; http://dx.doi.org/10.14989/doctor.k18300.

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

Council of Science Editors:

Morimoto M. Development of Highly Efficient Synthetic Reactions Catalyzed by Transition Metals : 遷移金属触媒を用いる高効率な合成反応の開発. [Thesis]. Kyoto University / 京都大学; 2014. Available from: http://hdl.handle.net/2433/188615 ; http://dx.doi.org/10.14989/doctor.k18300

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


Kyoto University / 京都大学

22. Kitano, Masaaki. Chemistry of meso-Free Subporphyrins : メゾフリーサブポルフィリンの化学.

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

新制・課程博士

甲第19516号

理博第4176号

Subjects/Keywords: porphyrinoids; subporphyrins; cross-coupling reactions; substitution; borylation

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APA (6th Edition):

Kitano, M. (2016). Chemistry of meso-Free Subporphyrins : メゾフリーサブポルフィリンの化学. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/215329 ; http://dx.doi.org/10.14989/doctor.k19516

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):

Kitano, Masaaki. “Chemistry of meso-Free Subporphyrins : メゾフリーサブポルフィリンの化学.” 2016. Thesis, Kyoto University / 京都大学. Accessed October 22, 2019. http://hdl.handle.net/2433/215329 ; http://dx.doi.org/10.14989/doctor.k19516.

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

MLA Handbook (7th Edition):

Kitano, Masaaki. “Chemistry of meso-Free Subporphyrins : メゾフリーサブポルフィリンの化学.” 2016. Web. 22 Oct 2019.

Vancouver:

Kitano M. Chemistry of meso-Free Subporphyrins : メゾフリーサブポルフィリンの化学. [Internet] [Thesis]. Kyoto University / 京都大学; 2016. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/2433/215329 ; http://dx.doi.org/10.14989/doctor.k19516.

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

Council of Science Editors:

Kitano M. Chemistry of meso-Free Subporphyrins : メゾフリーサブポルフィリンの化学. [Thesis]. Kyoto University / 京都大学; 2016. Available from: http://hdl.handle.net/2433/215329 ; http://dx.doi.org/10.14989/doctor.k19516

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


Kyoto University / 京都大学

23. Yamamoto, Yutaro. Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents : ルイス酸性を有するホウ素反応剤や有機ケイ素反応剤を用いたパラジウム触媒による塩化アリールの変換反応に関する研究.

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

新制・課程博士

甲第20205号

理博第4290号

Subjects/Keywords: palladium; aryl chloride; borylation; hydrodechlorination; cross-coupling reactions

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APA (6th Edition):

Yamamoto, Y. (2017). Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents : ルイス酸性を有するホウ素反応剤や有機ケイ素反応剤を用いたパラジウム触媒による塩化アリールの変換反応に関する研究. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/225430 ; http://dx.doi.org/10.14989/doctor.k20205

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):

Yamamoto, Yutaro. “Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents : ルイス酸性を有するホウ素反応剤や有機ケイ素反応剤を用いたパラジウム触媒による塩化アリールの変換反応に関する研究.” 2017. Thesis, Kyoto University / 京都大学. Accessed October 22, 2019. http://hdl.handle.net/2433/225430 ; http://dx.doi.org/10.14989/doctor.k20205.

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

MLA Handbook (7th Edition):

Yamamoto, Yutaro. “Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents : ルイス酸性を有するホウ素反応剤や有機ケイ素反応剤を用いたパラジウム触媒による塩化アリールの変換反応に関する研究.” 2017. Web. 22 Oct 2019.

Vancouver:

Yamamoto Y. Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents : ルイス酸性を有するホウ素反応剤や有機ケイ素反応剤を用いたパラジウム触媒による塩化アリールの変換反応に関する研究. [Internet] [Thesis]. Kyoto University / 京都大学; 2017. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/2433/225430 ; http://dx.doi.org/10.14989/doctor.k20205.

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

Council of Science Editors:

Yamamoto Y. Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents : ルイス酸性を有するホウ素反応剤や有機ケイ素反応剤を用いたパラジウム触媒による塩化アリールの変換反応に関する研究. [Thesis]. Kyoto University / 京都大学; 2017. Available from: http://hdl.handle.net/2433/225430 ; http://dx.doi.org/10.14989/doctor.k20205

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


Kyoto University

24. Kitano, Masaaki. Chemistry of meso-Free Subporphyrins .

Degree: 2016, Kyoto University

Subjects/Keywords: porphyrinoids; subporphyrins; cross-coupling reactions; substitution; borylation

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

APA (6th Edition):

Kitano, M. (2016). Chemistry of meso-Free Subporphyrins . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/215329

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):

Kitano, Masaaki. “Chemistry of meso-Free Subporphyrins .” 2016. Thesis, Kyoto University. Accessed October 22, 2019. http://hdl.handle.net/2433/215329.

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

MLA Handbook (7th Edition):

Kitano, Masaaki. “Chemistry of meso-Free Subporphyrins .” 2016. Web. 22 Oct 2019.

Vancouver:

Kitano M. Chemistry of meso-Free Subporphyrins . [Internet] [Thesis]. Kyoto University; 2016. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/2433/215329.

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

Council of Science Editors:

Kitano M. Chemistry of meso-Free Subporphyrins . [Thesis]. Kyoto University; 2016. Available from: http://hdl.handle.net/2433/215329

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


Kyoto University

25. Yamamoto, Yutaro. Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents .

Degree: 2017, Kyoto University

Subjects/Keywords: palladium; aryl chloride; borylation; hydrodechlorination; cross-coupling reactions

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APA (6th Edition):

Yamamoto, Y. (2017). Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/225430

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):

Yamamoto, Yutaro. “Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents .” 2017. Thesis, Kyoto University. Accessed October 22, 2019. http://hdl.handle.net/2433/225430.

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

MLA Handbook (7th Edition):

Yamamoto, Yutaro. “Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents .” 2017. Web. 22 Oct 2019.

Vancouver:

Yamamoto Y. Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents . [Internet] [Thesis]. Kyoto University; 2017. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/2433/225430.

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

Council of Science Editors:

Yamamoto Y. Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents . [Thesis]. Kyoto University; 2017. Available from: http://hdl.handle.net/2433/225430

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

26. Morimoto, Masao. Development of Highly Efficient Synthetic Reactions Catalyzed by Transition Metals .

Degree: 2014, Kyoto University

Subjects/Keywords: transition metal catalyst; metalacycle; cycloaddition; borylation; amination

Page 1 Page 2 Page 3

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APA (6th Edition):

Morimoto, M. (2014). Development of Highly Efficient Synthetic Reactions Catalyzed by Transition Metals . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/188615

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):

Morimoto, Masao. “Development of Highly Efficient Synthetic Reactions Catalyzed by Transition Metals .” 2014. Thesis, Kyoto University. Accessed October 22, 2019. http://hdl.handle.net/2433/188615.

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

MLA Handbook (7th Edition):

Morimoto, Masao. “Development of Highly Efficient Synthetic Reactions Catalyzed by Transition Metals .” 2014. Web. 22 Oct 2019.

Vancouver:

Morimoto M. Development of Highly Efficient Synthetic Reactions Catalyzed by Transition Metals . [Internet] [Thesis]. Kyoto University; 2014. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/2433/188615.

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

Council of Science Editors:

Morimoto M. Development of Highly Efficient Synthetic Reactions Catalyzed by Transition Metals . [Thesis]. Kyoto University; 2014. Available from: http://hdl.handle.net/2433/188615

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


University of Manchester

27. Crossley, Daniel. Directed C-H Borylation for the Synthesis of Fused and Ladder Type Conjugated Oligomers and Polymers.

Degree: 2016, University of Manchester

The synthesis, photophysical and electronic properties of a series of novel boron containing fused and ladder type donor−acceptor (D-A) oligomers and polymers are reported. The… (more)

Subjects/Keywords: Boron; Donor-Acceptor Compounds; OLEDs; Polymers; Near Infra-red Emission; Organoboron; Direct C-H Electrophilic Borylation

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

APA (6th Edition):

Crossley, D. (2016). Directed C-H Borylation for the Synthesis of Fused and Ladder Type Conjugated Oligomers and Polymers. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301616

Chicago Manual of Style (16th Edition):

Crossley, Daniel. “Directed C-H Borylation for the Synthesis of Fused and Ladder Type Conjugated Oligomers and Polymers.” 2016. Doctoral Dissertation, University of Manchester. Accessed October 22, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301616.

MLA Handbook (7th Edition):

Crossley, Daniel. “Directed C-H Borylation for the Synthesis of Fused and Ladder Type Conjugated Oligomers and Polymers.” 2016. Web. 22 Oct 2019.

Vancouver:

Crossley D. Directed C-H Borylation for the Synthesis of Fused and Ladder Type Conjugated Oligomers and Polymers. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2019 Oct 22]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301616.

Council of Science Editors:

Crossley D. Directed C-H Borylation for the Synthesis of Fused and Ladder Type Conjugated Oligomers and Polymers. [Doctoral Dissertation]. University of Manchester; 2016. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301616


Kyoto University

28. Semba, Kazuhiko. Highly Efficient Catalytic Transformations of Unsaturated Compounds via Ligand-Induced Selective Addition of Copper Species .

Degree: 2013, Kyoto University

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 . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/174888

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 .” 2013. Thesis, Kyoto University. Accessed October 22, 2019. http://hdl.handle.net/2433/174888.

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 .” 2013. Web. 22 Oct 2019.

Vancouver:

Semba K. Highly Efficient Catalytic Transformations of Unsaturated Compounds via Ligand-Induced Selective Addition of Copper Species . [Internet] [Thesis]. Kyoto University; 2013. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/2433/174888.

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 . [Thesis]. Kyoto University; 2013. Available from: http://hdl.handle.net/2433/174888

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

29. Moore, Brandon. HIGHLY SELECTIVE RHODIUM-CATALYZED C-H BORYLATIONS IN PREPARATION OF SUBSTRATES FOR SUZUKI-MIYAURA CROSS-COUPLINGS: MONO- AND CHEMOSELECTIVE FORMATION OF AROMATIC COMPOUNDS .

Degree: Chemistry, 2015, Queens University

 The advent of the Suzuki–Miyaura cross–coupling reaction and its significance to the synthesis of new carbon–carbon bonds has increased the demand for efficient routes to… (more)

Subjects/Keywords: Cross-Coupling; Suzuki; Borylation; Heck; Transition Metal; C-H Activation; Palladium; Boronic Ester; Catalysis; Carbenes; Chemoselective; Regioselective; NHC; Arylation; Boron; Rhodium

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APA (6th Edition):

Moore, B. (2015). HIGHLY SELECTIVE RHODIUM-CATALYZED C-H BORYLATIONS IN PREPARATION OF SUBSTRATES FOR SUZUKI-MIYAURA CROSS-COUPLINGS: MONO- AND CHEMOSELECTIVE FORMATION OF AROMATIC COMPOUNDS . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/12795

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):

Moore, Brandon. “HIGHLY SELECTIVE RHODIUM-CATALYZED C-H BORYLATIONS IN PREPARATION OF SUBSTRATES FOR SUZUKI-MIYAURA CROSS-COUPLINGS: MONO- AND CHEMOSELECTIVE FORMATION OF AROMATIC COMPOUNDS .” 2015. Thesis, Queens University. Accessed October 22, 2019. http://hdl.handle.net/1974/12795.

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

MLA Handbook (7th Edition):

Moore, Brandon. “HIGHLY SELECTIVE RHODIUM-CATALYZED C-H BORYLATIONS IN PREPARATION OF SUBSTRATES FOR SUZUKI-MIYAURA CROSS-COUPLINGS: MONO- AND CHEMOSELECTIVE FORMATION OF AROMATIC COMPOUNDS .” 2015. Web. 22 Oct 2019.

Vancouver:

Moore B. HIGHLY SELECTIVE RHODIUM-CATALYZED C-H BORYLATIONS IN PREPARATION OF SUBSTRATES FOR SUZUKI-MIYAURA CROSS-COUPLINGS: MONO- AND CHEMOSELECTIVE FORMATION OF AROMATIC COMPOUNDS . [Internet] [Thesis]. Queens University; 2015. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1974/12795.

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

Council of Science Editors:

Moore B. HIGHLY SELECTIVE RHODIUM-CATALYZED C-H BORYLATIONS IN PREPARATION OF SUBSTRATES FOR SUZUKI-MIYAURA CROSS-COUPLINGS: MONO- AND CHEMOSELECTIVE FORMATION OF AROMATIC COMPOUNDS . [Thesis]. Queens University; 2015. Available from: http://hdl.handle.net/1974/12795

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


University of Florida

30. Hirsch-Weil, Dimitri. Development of New Chiral Diaminocarbene Ligands and Their Applications in Copper-Catalyzed Reactions.

Degree: PhD, Chemistry, 2010, University of Florida

 DEVELOPMENT OF NEW CHIRAL DIAMINOCARBENE LIGANDS AND THEIR APPLICATIONS IN COPPER-CATALYZED REACTIONS By Dimitri Hirsch-Weil August 2010 Chair: Sukwon Hong Major: Organic Chemistry N-Heterocyclic carbene… (more)

Subjects/Keywords: Alkylation; Amines; Carbenes; Chlorides; Flasks; Ligands; Phenyls; Reagents; Room temperature; Solvents; acyclic, adc, alkylation, allylic, asymmetric, borylation, carbene, catalysis, chiral, copper, diaminocarbene, enantioselective, heterocyclic, isoquinoline, ligand, nhc

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APA (6th Edition):

Hirsch-Weil, D. (2010). Development of New Chiral Diaminocarbene Ligands and Their Applications in Copper-Catalyzed Reactions. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0041923

Chicago Manual of Style (16th Edition):

Hirsch-Weil, Dimitri. “Development of New Chiral Diaminocarbene Ligands and Their Applications in Copper-Catalyzed Reactions.” 2010. Doctoral Dissertation, University of Florida. Accessed October 22, 2019. http://ufdc.ufl.edu/UFE0041923.

MLA Handbook (7th Edition):

Hirsch-Weil, Dimitri. “Development of New Chiral Diaminocarbene Ligands and Their Applications in Copper-Catalyzed Reactions.” 2010. Web. 22 Oct 2019.

Vancouver:

Hirsch-Weil D. Development of New Chiral Diaminocarbene Ligands and Their Applications in Copper-Catalyzed Reactions. [Internet] [Doctoral dissertation]. University of Florida; 2010. [cited 2019 Oct 22]. Available from: http://ufdc.ufl.edu/UFE0041923.

Council of Science Editors:

Hirsch-Weil D. Development of New Chiral Diaminocarbene Ligands and Their Applications in Copper-Catalyzed Reactions. [Doctoral Dissertation]. University of Florida; 2010. Available from: http://ufdc.ufl.edu/UFE0041923

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