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You searched for subject:(Asymmetric Catalysis). Showing records 1 – 30 of 355 total matches.

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University of Oxford

1. Maciver, Eleanor E. Asymmetric electrocyclic reactions.

Degree: PhD, 2013, University of Oxford

 Pericyclic reactions are a class of transformations that comprise sigmatropic rearrangements, group transfer reactions, cycloadditions and electrocyclic reactions. Since Woodward and Hoffmann rationalized the mechanism… (more)

Subjects/Keywords: 547; Asymmetric catalysis; Electrocyclization; Asymmetric; Catalysis

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APA (6th Edition):

Maciver, E. E. (2013). Asymmetric electrocyclic reactions. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:17ba3cb0-0c62-406a-bed4-14c410a45918 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.588436

Chicago Manual of Style (16th Edition):

Maciver, Eleanor E. “Asymmetric electrocyclic reactions.” 2013. Doctoral Dissertation, University of Oxford. Accessed September 23, 2020. http://ora.ox.ac.uk/objects/uuid:17ba3cb0-0c62-406a-bed4-14c410a45918 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.588436.

MLA Handbook (7th Edition):

Maciver, Eleanor E. “Asymmetric electrocyclic reactions.” 2013. Web. 23 Sep 2020.

Vancouver:

Maciver EE. Asymmetric electrocyclic reactions. [Internet] [Doctoral dissertation]. University of Oxford; 2013. [cited 2020 Sep 23]. Available from: http://ora.ox.ac.uk/objects/uuid:17ba3cb0-0c62-406a-bed4-14c410a45918 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.588436.

Council of Science Editors:

Maciver EE. Asymmetric electrocyclic reactions. [Doctoral Dissertation]. University of Oxford; 2013. Available from: http://ora.ox.ac.uk/objects/uuid:17ba3cb0-0c62-406a-bed4-14c410a45918 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.588436


University of Notre Dame

2. Eric C. Hansen. Development and Applications of Quantum to Molecular Mechanics (Q2MM)</h1>.

Degree: Chemistry and Biochemistry, 2017, University of Notre Dame

Asymmetric synthesis is a major focus in modern organic chemistry. Experimentally screening for selective ligands is a cumbersome process, and provides only indirect insight… (more)

Subjects/Keywords: Chemistry; Asymmetric catalysis

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APA (6th Edition):

Hansen, E. C. (2017). Development and Applications of Quantum to Molecular Mechanics (Q2MM)</h1>. (Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/wd375t37h4h

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):

Hansen, Eric C.. “Development and Applications of Quantum to Molecular Mechanics (Q2MM)</h1>.” 2017. Thesis, University of Notre Dame. Accessed September 23, 2020. https://curate.nd.edu/show/wd375t37h4h.

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

MLA Handbook (7th Edition):

Hansen, Eric C.. “Development and Applications of Quantum to Molecular Mechanics (Q2MM)</h1>.” 2017. Web. 23 Sep 2020.

Vancouver:

Hansen EC. Development and Applications of Quantum to Molecular Mechanics (Q2MM)</h1>. [Internet] [Thesis]. University of Notre Dame; 2017. [cited 2020 Sep 23]. Available from: https://curate.nd.edu/show/wd375t37h4h.

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

Council of Science Editors:

Hansen EC. Development and Applications of Quantum to Molecular Mechanics (Q2MM)</h1>. [Thesis]. University of Notre Dame; 2017. Available from: https://curate.nd.edu/show/wd375t37h4h

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


Brock University

3. Zaifman, Joshua David. Stereoselective synthesis of substituted hexahydro-3a,4a-diazacyclopentaphenanthren-4-ones and aminoferrocenes .

Degree: Department of Chemistry, 2011, Brock University

 This thesis explored the development of several methodologies for the stereoselective construction of ligand frameworks and some of their applications. The first segment concerns the… (more)

Subjects/Keywords: Asymmetric synthesis; Catalysis

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APA (6th Edition):

Zaifman, J. D. (2011). Stereoselective synthesis of substituted hexahydro-3a,4a-diazacyclopentaphenanthren-4-ones and aminoferrocenes . (Thesis). Brock University. Retrieved from http://hdl.handle.net/10464/3383

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):

Zaifman, Joshua David. “Stereoselective synthesis of substituted hexahydro-3a,4a-diazacyclopentaphenanthren-4-ones and aminoferrocenes .” 2011. Thesis, Brock University. Accessed September 23, 2020. http://hdl.handle.net/10464/3383.

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

MLA Handbook (7th Edition):

Zaifman, Joshua David. “Stereoselective synthesis of substituted hexahydro-3a,4a-diazacyclopentaphenanthren-4-ones and aminoferrocenes .” 2011. Web. 23 Sep 2020.

Vancouver:

Zaifman JD. Stereoselective synthesis of substituted hexahydro-3a,4a-diazacyclopentaphenanthren-4-ones and aminoferrocenes . [Internet] [Thesis]. Brock University; 2011. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/10464/3383.

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

Council of Science Editors:

Zaifman JD. Stereoselective synthesis of substituted hexahydro-3a,4a-diazacyclopentaphenanthren-4-ones and aminoferrocenes . [Thesis]. Brock University; 2011. Available from: http://hdl.handle.net/10464/3383

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


University of California – Berkeley

4. Brown, Casey Jameson. Asymmetric and Organometallic Catalysis Mediated by a Chiral Supramolecular Host.

Degree: Chemistry, 2011, University of California – Berkeley

 Chapter 1. An overview of supramolecular catalysis is presented with attention to the diverse strategies used in developing these materials. Different strategies for the design… (more)

Subjects/Keywords: Chemistry; asymmetric; catalysis; organometallic; supramolecular

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APA (6th Edition):

Brown, C. J. (2011). Asymmetric and Organometallic Catalysis Mediated by a Chiral Supramolecular Host. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/7jv7m4wh

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):

Brown, Casey Jameson. “Asymmetric and Organometallic Catalysis Mediated by a Chiral Supramolecular Host.” 2011. Thesis, University of California – Berkeley. Accessed September 23, 2020. http://www.escholarship.org/uc/item/7jv7m4wh.

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

MLA Handbook (7th Edition):

Brown, Casey Jameson. “Asymmetric and Organometallic Catalysis Mediated by a Chiral Supramolecular Host.” 2011. Web. 23 Sep 2020.

Vancouver:

Brown CJ. Asymmetric and Organometallic Catalysis Mediated by a Chiral Supramolecular Host. [Internet] [Thesis]. University of California – Berkeley; 2011. [cited 2020 Sep 23]. Available from: http://www.escholarship.org/uc/item/7jv7m4wh.

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

Council of Science Editors:

Brown CJ. Asymmetric and Organometallic Catalysis Mediated by a Chiral Supramolecular Host. [Thesis]. University of California – Berkeley; 2011. Available from: http://www.escholarship.org/uc/item/7jv7m4wh

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

5. Minerali, Eni. Asymmetric synthesis of enantioenriched spirocycles via a chiral Brønsted acid catalyzed desymmetrization.

Degree: 2019, NC Docks

Asymmetric methodologies are very important as they allow chemists to produce significant quantities of complex chiral molecules as enantiopure or enantioenriched compounds. The Petersen group… (more)

Subjects/Keywords: Asymmetric synthesis; Chirality; Catalysis

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APA (6th Edition):

Minerali, E. (2019). Asymmetric synthesis of enantioenriched spirocycles via a chiral Brønsted acid catalyzed desymmetrization. (Thesis). NC Docks. Retrieved from http://libres.uncg.edu/ir/uncg/f/Minerali_uncg_0154M_12848.pdf

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):

Minerali, Eni. “Asymmetric synthesis of enantioenriched spirocycles via a chiral Brønsted acid catalyzed desymmetrization.” 2019. Thesis, NC Docks. Accessed September 23, 2020. http://libres.uncg.edu/ir/uncg/f/Minerali_uncg_0154M_12848.pdf.

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

MLA Handbook (7th Edition):

Minerali, Eni. “Asymmetric synthesis of enantioenriched spirocycles via a chiral Brønsted acid catalyzed desymmetrization.” 2019. Web. 23 Sep 2020.

Vancouver:

Minerali E. Asymmetric synthesis of enantioenriched spirocycles via a chiral Brønsted acid catalyzed desymmetrization. [Internet] [Thesis]. NC Docks; 2019. [cited 2020 Sep 23]. Available from: http://libres.uncg.edu/ir/uncg/f/Minerali_uncg_0154M_12848.pdf.

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

Council of Science Editors:

Minerali E. Asymmetric synthesis of enantioenriched spirocycles via a chiral Brønsted acid catalyzed desymmetrization. [Thesis]. NC Docks; 2019. Available from: http://libres.uncg.edu/ir/uncg/f/Minerali_uncg_0154M_12848.pdf

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


Texas A&M University

6. Ghosh, Subrata Kumar. The Development of New Classes of Enantioselective Hydrogen Bond Donor Catalysts for Organic Synthesis Based upon Werner Complexes.

Degree: PhD, Chemistry, 2017, Texas A&M University

 In this dissertation, the development of highly effective, chiral monofunctional and bifunctional hydrogen bond donor catalysts based on cobalt(III) Werner complexes and their applications in… (more)

Subjects/Keywords: Chiral; asymmetric; catalysis; cobalt; fluorous

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APA (6th Edition):

Ghosh, S. K. (2017). The Development of New Classes of Enantioselective Hydrogen Bond Donor Catalysts for Organic Synthesis Based upon Werner Complexes. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/169551

Chicago Manual of Style (16th Edition):

Ghosh, Subrata Kumar. “The Development of New Classes of Enantioselective Hydrogen Bond Donor Catalysts for Organic Synthesis Based upon Werner Complexes.” 2017. Doctoral Dissertation, Texas A&M University. Accessed September 23, 2020. http://hdl.handle.net/1969.1/169551.

MLA Handbook (7th Edition):

Ghosh, Subrata Kumar. “The Development of New Classes of Enantioselective Hydrogen Bond Donor Catalysts for Organic Synthesis Based upon Werner Complexes.” 2017. Web. 23 Sep 2020.

Vancouver:

Ghosh SK. The Development of New Classes of Enantioselective Hydrogen Bond Donor Catalysts for Organic Synthesis Based upon Werner Complexes. [Internet] [Doctoral dissertation]. Texas A&M University; 2017. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1969.1/169551.

Council of Science Editors:

Ghosh SK. The Development of New Classes of Enantioselective Hydrogen Bond Donor Catalysts for Organic Synthesis Based upon Werner Complexes. [Doctoral Dissertation]. Texas A&M University; 2017. Available from: http://hdl.handle.net/1969.1/169551


Colorado State University

7. White, Nicholas Andrew. Enantioselective β-functionalization of enals via N-heterocyclic carbene catalysis.

Degree: PhD, Chemistry, 2015, Colorado State University

 A series of δ-nitroesters were synthesized through the N-heterocyclic carbene catalyzed coupling of enals and nitroalkenes. The asymmetric coupling of these substrates via the homoenolate… (more)

Subjects/Keywords: asymmetric; carbene; catalysis; organic

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APA (6th Edition):

White, N. A. (2015). Enantioselective β-functionalization of enals via N-heterocyclic carbene catalysis. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/170358

Chicago Manual of Style (16th Edition):

White, Nicholas Andrew. “Enantioselective β-functionalization of enals via N-heterocyclic carbene catalysis.” 2015. Doctoral Dissertation, Colorado State University. Accessed September 23, 2020. http://hdl.handle.net/10217/170358.

MLA Handbook (7th Edition):

White, Nicholas Andrew. “Enantioselective β-functionalization of enals via N-heterocyclic carbene catalysis.” 2015. Web. 23 Sep 2020.

Vancouver:

White NA. Enantioselective β-functionalization of enals via N-heterocyclic carbene catalysis. [Internet] [Doctoral dissertation]. Colorado State University; 2015. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/10217/170358.

Council of Science Editors:

White NA. Enantioselective β-functionalization of enals via N-heterocyclic carbene catalysis. [Doctoral Dissertation]. Colorado State University; 2015. Available from: http://hdl.handle.net/10217/170358


Rice University

8. Sambasivan, Ramya. Rh(II) metallopeptides for asymmetric catalysis.

Degree: PhD, Natural Sciences, 2015, Rice University

 The development of peptides as chiral ligands for asymmetric Rh(II) catalysis is discussed in this work. Mother Nature’s solution to chiral ligand design is to… (more)

Subjects/Keywords: metallopeptide; asymmetric catalysis; rhodium catalyst

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APA (6th Edition):

Sambasivan, R. (2015). Rh(II) metallopeptides for asymmetric catalysis. (Doctoral Dissertation). Rice University. Retrieved from http://hdl.handle.net/1911/95526

Chicago Manual of Style (16th Edition):

Sambasivan, Ramya. “Rh(II) metallopeptides for asymmetric catalysis.” 2015. Doctoral Dissertation, Rice University. Accessed September 23, 2020. http://hdl.handle.net/1911/95526.

MLA Handbook (7th Edition):

Sambasivan, Ramya. “Rh(II) metallopeptides for asymmetric catalysis.” 2015. Web. 23 Sep 2020.

Vancouver:

Sambasivan R. Rh(II) metallopeptides for asymmetric catalysis. [Internet] [Doctoral dissertation]. Rice University; 2015. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1911/95526.

Council of Science Editors:

Sambasivan R. Rh(II) metallopeptides for asymmetric catalysis. [Doctoral Dissertation]. Rice University; 2015. Available from: http://hdl.handle.net/1911/95526

9. Stache, Erin Elizabeth. Dual nickel- and photoredox-catalyzed enantioselective desymmetrization of meso anhydrides and C-O bond activation via phosphines and photoredox catalysis.

Degree: PhD, Chemistry, 2018, Colorado State University

 Described herein is the application of photoredox catalysis in the development of new synthetic methods. A dual nickel- and photoredox catalyzed desymmetrization of meso succinic… (more)

Subjects/Keywords: nickel catalysis; photochemistry; organic synthesis; asymmetric catalysis

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APA (6th Edition):

Stache, E. E. (2018). Dual nickel- and photoredox-catalyzed enantioselective desymmetrization of meso anhydrides and C-O bond activation via phosphines and photoredox catalysis. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/191328

Chicago Manual of Style (16th Edition):

Stache, Erin Elizabeth. “Dual nickel- and photoredox-catalyzed enantioselective desymmetrization of meso anhydrides and C-O bond activation via phosphines and photoredox catalysis.” 2018. Doctoral Dissertation, Colorado State University. Accessed September 23, 2020. http://hdl.handle.net/10217/191328.

MLA Handbook (7th Edition):

Stache, Erin Elizabeth. “Dual nickel- and photoredox-catalyzed enantioselective desymmetrization of meso anhydrides and C-O bond activation via phosphines and photoredox catalysis.” 2018. Web. 23 Sep 2020.

Vancouver:

Stache EE. Dual nickel- and photoredox-catalyzed enantioselective desymmetrization of meso anhydrides and C-O bond activation via phosphines and photoredox catalysis. [Internet] [Doctoral dissertation]. Colorado State University; 2018. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/10217/191328.

Council of Science Editors:

Stache EE. Dual nickel- and photoredox-catalyzed enantioselective desymmetrization of meso anhydrides and C-O bond activation via phosphines and photoredox catalysis. [Doctoral Dissertation]. Colorado State University; 2018. Available from: http://hdl.handle.net/10217/191328


Colorado State University

10. Vora, Harit. N-heterocyclic carbene catalyzed α-redox reaction: catalytic synthesis of amides and carboxylic acids.

Degree: PhD, Chemistry, 2011, Colorado State University

 N-heterocyclic carbene catalyzed α-redox reaction has been utilized towards the catalytic synthesis of amides utilizing amines and substoichiometric quantities of an acyl transfer reagent in… (more)

Subjects/Keywords: synthesis; NHC catalysis; organic chemistry; asymmetric; catalysis

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APA (6th Edition):

Vora, H. (2011). N-heterocyclic carbene catalyzed α-redox reaction: catalytic synthesis of amides and carboxylic acids. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/52114

Chicago Manual of Style (16th Edition):

Vora, Harit. “N-heterocyclic carbene catalyzed α-redox reaction: catalytic synthesis of amides and carboxylic acids.” 2011. Doctoral Dissertation, Colorado State University. Accessed September 23, 2020. http://hdl.handle.net/10217/52114.

MLA Handbook (7th Edition):

Vora, Harit. “N-heterocyclic carbene catalyzed α-redox reaction: catalytic synthesis of amides and carboxylic acids.” 2011. Web. 23 Sep 2020.

Vancouver:

Vora H. N-heterocyclic carbene catalyzed α-redox reaction: catalytic synthesis of amides and carboxylic acids. [Internet] [Doctoral dissertation]. Colorado State University; 2011. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/10217/52114.

Council of Science Editors:

Vora H. N-heterocyclic carbene catalyzed α-redox reaction: catalytic synthesis of amides and carboxylic acids. [Doctoral Dissertation]. Colorado State University; 2011. Available from: http://hdl.handle.net/10217/52114


University of St. Andrews

11. Durrani, Jamie T. Palladium catalysed asymmetric hydroxy- and alkoxycarbonylation of alkenes .

Degree: 2015, University of St. Andrews

 Palladium catalysed asymmetric hydroxy- and alkoxycarbonylation reactions of alkenes have the potential to deliver valuable chiral carboxylic acid and ester building blocks from cheap feedstocks:… (more)

Subjects/Keywords: Hydroxycarbonylation; Alkoxycarbonylation; Carbonylation; Asymmetric catalysis; Homogeneous catalysis

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APA (6th Edition):

Durrani, J. T. (2015). Palladium catalysed asymmetric hydroxy- and alkoxycarbonylation of alkenes . (Thesis). University of St. Andrews. Retrieved from http://hdl.handle.net/10023/6276

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):

Durrani, Jamie T. “Palladium catalysed asymmetric hydroxy- and alkoxycarbonylation of alkenes .” 2015. Thesis, University of St. Andrews. Accessed September 23, 2020. http://hdl.handle.net/10023/6276.

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

MLA Handbook (7th Edition):

Durrani, Jamie T. “Palladium catalysed asymmetric hydroxy- and alkoxycarbonylation of alkenes .” 2015. Web. 23 Sep 2020.

Vancouver:

Durrani JT. Palladium catalysed asymmetric hydroxy- and alkoxycarbonylation of alkenes . [Internet] [Thesis]. University of St. Andrews; 2015. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/10023/6276.

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

Council of Science Editors:

Durrani JT. Palladium catalysed asymmetric hydroxy- and alkoxycarbonylation of alkenes . [Thesis]. University of St. Andrews; 2015. Available from: http://hdl.handle.net/10023/6276

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


Université Catholique de Louvain

12. Nahra, Fady. Study of new reactions catalysed by copper(I) complexes : investigation of domino catalysis- and dual catalysis-type reactions.

Degree: 2013, Université Catholique de Louvain

In this thesis we are going to first discuss the application of a copper hydride system, which was previously developed in our lab, to new… (more)

Subjects/Keywords: Asymmetric catalysis; Copper(I); Palladium(0); Domino catalysis; Dual catalysis

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APA (6th Edition):

Nahra, F. (2013). Study of new reactions catalysed by copper(I) complexes : investigation of domino catalysis- and dual catalysis-type reactions. (Thesis). Université Catholique de Louvain. Retrieved from http://hdl.handle.net/2078.1/133426

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):

Nahra, Fady. “Study of new reactions catalysed by copper(I) complexes : investigation of domino catalysis- and dual catalysis-type reactions.” 2013. Thesis, Université Catholique de Louvain. Accessed September 23, 2020. http://hdl.handle.net/2078.1/133426.

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

MLA Handbook (7th Edition):

Nahra, Fady. “Study of new reactions catalysed by copper(I) complexes : investigation of domino catalysis- and dual catalysis-type reactions.” 2013. Web. 23 Sep 2020.

Vancouver:

Nahra F. Study of new reactions catalysed by copper(I) complexes : investigation of domino catalysis- and dual catalysis-type reactions. [Internet] [Thesis]. Université Catholique de Louvain; 2013. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/2078.1/133426.

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

Council of Science Editors:

Nahra F. Study of new reactions catalysed by copper(I) complexes : investigation of domino catalysis- and dual catalysis-type reactions. [Thesis]. Université Catholique de Louvain; 2013. Available from: http://hdl.handle.net/2078.1/133426

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


University of St. Andrews

13. Gilbert, Sophie Hannah. Rhodium catalysed asymmetric synthesis of tertiary amines .

Degree: 2020, University of St. Andrews

 The asymmetric synthesis of tertiary amines is a highly desirable goal, but far fewer efficient synthetic methods exist for their synthesis, relative to primary and… (more)

Subjects/Keywords: Chemistry; Catalysis; Homogeneous catalysis; Hydrogenation; Asymmetric catalysis; Chiral amines; Organometallic chemistry

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APA (6th Edition):

Gilbert, S. H. (2020). Rhodium catalysed asymmetric synthesis of tertiary amines . (Thesis). University of St. Andrews. Retrieved from http://hdl.handle.net/10023/19528

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):

Gilbert, Sophie Hannah. “Rhodium catalysed asymmetric synthesis of tertiary amines .” 2020. Thesis, University of St. Andrews. Accessed September 23, 2020. http://hdl.handle.net/10023/19528.

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

MLA Handbook (7th Edition):

Gilbert, Sophie Hannah. “Rhodium catalysed asymmetric synthesis of tertiary amines .” 2020. Web. 23 Sep 2020.

Vancouver:

Gilbert SH. Rhodium catalysed asymmetric synthesis of tertiary amines . [Internet] [Thesis]. University of St. Andrews; 2020. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/10023/19528.

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

Council of Science Editors:

Gilbert SH. Rhodium catalysed asymmetric synthesis of tertiary amines . [Thesis]. University of St. Andrews; 2020. Available from: http://hdl.handle.net/10023/19528

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


University of California – Berkeley

14. Neel, Andrew James. Toward the Rational Design of Asymmetric Catalysts using Attractive Non-Covalent Interactions and Design Elements.

Degree: Chemistry, 2016, University of California – Berkeley

 Throughout my doctoral studies, I have endeavored to address the question of how to rationally design chiral catalysts to control enantioselectivity in a predictable fashion.… (more)

Subjects/Keywords: Chemistry; Asymmetric Catalysis; Organic Synthesis; Organocatalysis

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APA (6th Edition):

Neel, A. J. (2016). Toward the Rational Design of Asymmetric Catalysts using Attractive Non-Covalent Interactions and Design Elements. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/34d2396n

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):

Neel, Andrew James. “Toward the Rational Design of Asymmetric Catalysts using Attractive Non-Covalent Interactions and Design Elements.” 2016. Thesis, University of California – Berkeley. Accessed September 23, 2020. http://www.escholarship.org/uc/item/34d2396n.

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

MLA Handbook (7th Edition):

Neel, Andrew James. “Toward the Rational Design of Asymmetric Catalysts using Attractive Non-Covalent Interactions and Design Elements.” 2016. Web. 23 Sep 2020.

Vancouver:

Neel AJ. Toward the Rational Design of Asymmetric Catalysts using Attractive Non-Covalent Interactions and Design Elements. [Internet] [Thesis]. University of California – Berkeley; 2016. [cited 2020 Sep 23]. Available from: http://www.escholarship.org/uc/item/34d2396n.

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

Council of Science Editors:

Neel AJ. Toward the Rational Design of Asymmetric Catalysts using Attractive Non-Covalent Interactions and Design Elements. [Thesis]. University of California – Berkeley; 2016. Available from: http://www.escholarship.org/uc/item/34d2396n

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


University of Alberta

15. Rauniyar, Vivek. Mechanistic Investigation, Development and Synthetic Applications of a Catalytic Enantioselective and Diastereoselective Allylboration Methodology.

Degree: PhD, Department of Chemistry, 2009, University of Alberta

 Over the past two decades and continuing on, carbonyl allylation chemistry has been a very useful and popular tool for the stereocontrolled formation of carbon-carbon… (more)

Subjects/Keywords: Asymmetric Catalysis, Allylboration, Allylboronate, Palmerolide A

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APA (6th Edition):

Rauniyar, V. (2009). Mechanistic Investigation, Development and Synthetic Applications of a Catalytic Enantioselective and Diastereoselective Allylboration Methodology. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/kw52j8708

Chicago Manual of Style (16th Edition):

Rauniyar, Vivek. “Mechanistic Investigation, Development and Synthetic Applications of a Catalytic Enantioselective and Diastereoselective Allylboration Methodology.” 2009. Doctoral Dissertation, University of Alberta. Accessed September 23, 2020. https://era.library.ualberta.ca/files/kw52j8708.

MLA Handbook (7th Edition):

Rauniyar, Vivek. “Mechanistic Investigation, Development and Synthetic Applications of a Catalytic Enantioselective and Diastereoselective Allylboration Methodology.” 2009. Web. 23 Sep 2020.

Vancouver:

Rauniyar V. Mechanistic Investigation, Development and Synthetic Applications of a Catalytic Enantioselective and Diastereoselective Allylboration Methodology. [Internet] [Doctoral dissertation]. University of Alberta; 2009. [cited 2020 Sep 23]. Available from: https://era.library.ualberta.ca/files/kw52j8708.

Council of Science Editors:

Rauniyar V. Mechanistic Investigation, Development and Synthetic Applications of a Catalytic Enantioselective and Diastereoselective Allylboration Methodology. [Doctoral Dissertation]. University of Alberta; 2009. Available from: https://era.library.ualberta.ca/files/kw52j8708


Penn State University

16. Li, Wei. Design and Synthesis of Chiral Ligands and Their Applications in Transition Metal-catalyzed Asymmetric Reactions.

Degree: 2012, Penn State University

 Transition metal catalyzed reactions are among the most powerful and direct approaches for the synthesis of organic molecules. During the past several decades, phosphorous-containing ligands… (more)

Subjects/Keywords: synthesis; chiral ligand; asymmetric catalysis; transition metal

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APA (6th Edition):

Li, W. (2012). Design and Synthesis of Chiral Ligands and Their Applications in Transition Metal-catalyzed Asymmetric Reactions. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/12770

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):

Li, Wei. “Design and Synthesis of Chiral Ligands and Their Applications in Transition Metal-catalyzed Asymmetric Reactions.” 2012. Thesis, Penn State University. Accessed September 23, 2020. https://submit-etda.libraries.psu.edu/catalog/12770.

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

MLA Handbook (7th Edition):

Li, Wei. “Design and Synthesis of Chiral Ligands and Their Applications in Transition Metal-catalyzed Asymmetric Reactions.” 2012. Web. 23 Sep 2020.

Vancouver:

Li W. Design and Synthesis of Chiral Ligands and Their Applications in Transition Metal-catalyzed Asymmetric Reactions. [Internet] [Thesis]. Penn State University; 2012. [cited 2020 Sep 23]. Available from: https://submit-etda.libraries.psu.edu/catalog/12770.

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

Council of Science Editors:

Li W. Design and Synthesis of Chiral Ligands and Their Applications in Transition Metal-catalyzed Asymmetric Reactions. [Thesis]. Penn State University; 2012. Available from: https://submit-etda.libraries.psu.edu/catalog/12770

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


Wayne State University

17. Averill, Derek James. Lanthanide-Based Precatalysts For Carbon-Carbon Bond-Forming Reactions In Aqueous Media.

Degree: PhD, Chemistry, 2014, Wayne State University

  The formation of carbon-carbon bonds is of great interest to synthetic chemists because these bonds make up the majority of biologically active compounds. The… (more)

Subjects/Keywords: Aqueous; Asymmetric; Catalysis; Europium; Lanthanide; Mukaiyama; Chemistry

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APA (6th Edition):

Averill, D. J. (2014). Lanthanide-Based Precatalysts For Carbon-Carbon Bond-Forming Reactions In Aqueous Media. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/1084

Chicago Manual of Style (16th Edition):

Averill, Derek James. “Lanthanide-Based Precatalysts For Carbon-Carbon Bond-Forming Reactions In Aqueous Media.” 2014. Doctoral Dissertation, Wayne State University. Accessed September 23, 2020. https://digitalcommons.wayne.edu/oa_dissertations/1084.

MLA Handbook (7th Edition):

Averill, Derek James. “Lanthanide-Based Precatalysts For Carbon-Carbon Bond-Forming Reactions In Aqueous Media.” 2014. Web. 23 Sep 2020.

Vancouver:

Averill DJ. Lanthanide-Based Precatalysts For Carbon-Carbon Bond-Forming Reactions In Aqueous Media. [Internet] [Doctoral dissertation]. Wayne State University; 2014. [cited 2020 Sep 23]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/1084.

Council of Science Editors:

Averill DJ. Lanthanide-Based Precatalysts For Carbon-Carbon Bond-Forming Reactions In Aqueous Media. [Doctoral Dissertation]. Wayne State University; 2014. Available from: https://digitalcommons.wayne.edu/oa_dissertations/1084


Universidade Nova

18. Zalewska, Karolina Anna Maria. Development of novel ionic liquids based on biological molecules.

Degree: 2015, Universidade Nova

 Ionic Liquids (ILs) belong to a class of compounds with unusual properties: very low vapour pressure; high chemical and thermal stability and the ability to… (more)

Subjects/Keywords: Ionic liquids; Biological molecules; Chirality; Asymmetric catalysis

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APA (6th Edition):

Zalewska, K. A. M. (2015). Development of novel ionic liquids based on biological molecules. (Thesis). Universidade Nova. Retrieved from http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/14075

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):

Zalewska, Karolina Anna Maria. “Development of novel ionic liquids based on biological molecules.” 2015. Thesis, Universidade Nova. Accessed September 23, 2020. http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/14075.

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

MLA Handbook (7th Edition):

Zalewska, Karolina Anna Maria. “Development of novel ionic liquids based on biological molecules.” 2015. Web. 23 Sep 2020.

Vancouver:

Zalewska KAM. Development of novel ionic liquids based on biological molecules. [Internet] [Thesis]. Universidade Nova; 2015. [cited 2020 Sep 23]. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/14075.

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

Council of Science Editors:

Zalewska KAM. Development of novel ionic liquids based on biological molecules. [Thesis]. Universidade Nova; 2015. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/14075

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


Colorado State University

19. Glover, Garrett S. Development of an asymmetric intermolecular stetter reaction and organocatalyst design.

Degree: MS(M.S.), Chemistry, 2012, Colorado State University

 The intermolecular Stetter represents a powerful carbon-carbon bond forming reaction that involves addition of an acyl anion equivalent to an untethered Michael acceptor. Despite the… (more)

Subjects/Keywords: asymmetric catalysis; Stetter reaction; organocatalysis; NHC; intermolecular

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APA (6th Edition):

Glover, G. S. (2012). Development of an asymmetric intermolecular stetter reaction and organocatalyst design. (Masters Thesis). Colorado State University. Retrieved from http://hdl.handle.net/10217/88358

Chicago Manual of Style (16th Edition):

Glover, Garrett S. “Development of an asymmetric intermolecular stetter reaction and organocatalyst design.” 2012. Masters Thesis, Colorado State University. Accessed September 23, 2020. http://hdl.handle.net/10217/88358.

MLA Handbook (7th Edition):

Glover, Garrett S. “Development of an asymmetric intermolecular stetter reaction and organocatalyst design.” 2012. Web. 23 Sep 2020.

Vancouver:

Glover GS. Development of an asymmetric intermolecular stetter reaction and organocatalyst design. [Internet] [Masters thesis]. Colorado State University; 2012. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/10217/88358.

Council of Science Editors:

Glover GS. Development of an asymmetric intermolecular stetter reaction and organocatalyst design. [Masters Thesis]. Colorado State University; 2012. Available from: http://hdl.handle.net/10217/88358


Colorado State University

20. Filloux, Claire M. Organocatalytic, Michael-Stetter reaction and rhodium(I)-catalyzed hydroheteroarylation of acrylates with benzoxazoles: reaction development and investigations into origins of enantioselectivity.

Degree: PhD, Chemistry, 2015, Colorado State University

 The chapters that follow describe two independent investigations. Both relay the development of experimental methods for the catalytic, asymmetric addition of carbon-hydrogen bonds to alkenes.… (more)

Subjects/Keywords: catalysis; organic; asymmetric; rhodium; N-heterocyclic carbene

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APA (6th Edition):

Filloux, C. M. (2015). Organocatalytic, Michael-Stetter reaction and rhodium(I)-catalyzed hydroheteroarylation of acrylates with benzoxazoles: reaction development and investigations into origins of enantioselectivity. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/166906

Chicago Manual of Style (16th Edition):

Filloux, Claire M. “Organocatalytic, Michael-Stetter reaction and rhodium(I)-catalyzed hydroheteroarylation of acrylates with benzoxazoles: reaction development and investigations into origins of enantioselectivity.” 2015. Doctoral Dissertation, Colorado State University. Accessed September 23, 2020. http://hdl.handle.net/10217/166906.

MLA Handbook (7th Edition):

Filloux, Claire M. “Organocatalytic, Michael-Stetter reaction and rhodium(I)-catalyzed hydroheteroarylation of acrylates with benzoxazoles: reaction development and investigations into origins of enantioselectivity.” 2015. Web. 23 Sep 2020.

Vancouver:

Filloux CM. Organocatalytic, Michael-Stetter reaction and rhodium(I)-catalyzed hydroheteroarylation of acrylates with benzoxazoles: reaction development and investigations into origins of enantioselectivity. [Internet] [Doctoral dissertation]. Colorado State University; 2015. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/10217/166906.

Council of Science Editors:

Filloux CM. Organocatalytic, Michael-Stetter reaction and rhodium(I)-catalyzed hydroheteroarylation of acrylates with benzoxazoles: reaction development and investigations into origins of enantioselectivity. [Doctoral Dissertation]. Colorado State University; 2015. Available from: http://hdl.handle.net/10217/166906


Colorado State University

21. Ozboya, Kerem. Development of an asymmetric NHC-catalyzed cascade reaction and studies towards the asymmetric aminomethylation of enals.

Degree: PhD, Chemistry, 2015, Colorado State University

 A cascade reaction is developed to form complex cyclopentanones using an asymmetric Michael/Benzoin sequence. This reaction employs simple aliphatic aldehydes and ketoesters in conjunction with… (more)

Subjects/Keywords: NHC; organocatalysis; organic synthesis; asymmetric catalysis

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APA (6th Edition):

Ozboya, K. (2015). Development of an asymmetric NHC-catalyzed cascade reaction and studies towards the asymmetric aminomethylation of enals. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/166865

Chicago Manual of Style (16th Edition):

Ozboya, Kerem. “Development of an asymmetric NHC-catalyzed cascade reaction and studies towards the asymmetric aminomethylation of enals.” 2015. Doctoral Dissertation, Colorado State University. Accessed September 23, 2020. http://hdl.handle.net/10217/166865.

MLA Handbook (7th Edition):

Ozboya, Kerem. “Development of an asymmetric NHC-catalyzed cascade reaction and studies towards the asymmetric aminomethylation of enals.” 2015. Web. 23 Sep 2020.

Vancouver:

Ozboya K. Development of an asymmetric NHC-catalyzed cascade reaction and studies towards the asymmetric aminomethylation of enals. [Internet] [Doctoral dissertation]. Colorado State University; 2015. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/10217/166865.

Council of Science Editors:

Ozboya K. Development of an asymmetric NHC-catalyzed cascade reaction and studies towards the asymmetric aminomethylation of enals. [Doctoral Dissertation]. Colorado State University; 2015. Available from: http://hdl.handle.net/10217/166865


Mississippi State University

22. Chakraborty, Amarraj. The method development for synthesizing chiral CCC-NHC Zr pincer complexes.

Degree: MS, Chemistry, 2015, Mississippi State University

  There are numerous classes of N-heterocyclic carbenes (NHCs) that have been synthesized since the discovery of stable NHCs in 1988. Their application as ligands… (more)

Subjects/Keywords: synthesis; Zr chemistry; organometallic chemistry; asymmetric catalysis

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APA (6th Edition):

Chakraborty, A. (2015). The method development for synthesizing chiral CCC-NHC Zr pincer complexes. (Masters Thesis). Mississippi State University. Retrieved from http://sun.library.msstate.edu/ETD-db/theses/available/etd-08062015-162047/ ;

Chicago Manual of Style (16th Edition):

Chakraborty, Amarraj. “The method development for synthesizing chiral CCC-NHC Zr pincer complexes.” 2015. Masters Thesis, Mississippi State University. Accessed September 23, 2020. http://sun.library.msstate.edu/ETD-db/theses/available/etd-08062015-162047/ ;.

MLA Handbook (7th Edition):

Chakraborty, Amarraj. “The method development for synthesizing chiral CCC-NHC Zr pincer complexes.” 2015. Web. 23 Sep 2020.

Vancouver:

Chakraborty A. The method development for synthesizing chiral CCC-NHC Zr pincer complexes. [Internet] [Masters thesis]. Mississippi State University; 2015. [cited 2020 Sep 23]. Available from: http://sun.library.msstate.edu/ETD-db/theses/available/etd-08062015-162047/ ;.

Council of Science Editors:

Chakraborty A. The method development for synthesizing chiral CCC-NHC Zr pincer complexes. [Masters Thesis]. Mississippi State University; 2015. Available from: http://sun.library.msstate.edu/ETD-db/theses/available/etd-08062015-162047/ ;


Boston College

23. Coombs, John Ryan. Platinum-Catalyzed Enantioselective Diboration of Terminal Alkenes and Vinyl Boronates: Construction of Multiborylated Compounds for Asymmetric Synthesis.

Degree: PhD, Chemistry, 2015, Boston College

 This dissertation will discuss in depth four main projects pertaining to the synthesis and utility of organoboronates for the construction of enantioenriched small molecules. First,… (more)

Subjects/Keywords: Asymmetric Catalysis; Boron-Wittig Reaction; Diboration

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APA (6th Edition):

Coombs, J. R. (2015). Platinum-Catalyzed Enantioselective Diboration of Terminal Alkenes and Vinyl Boronates: Construction of Multiborylated Compounds for Asymmetric Synthesis. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:104624

Chicago Manual of Style (16th Edition):

Coombs, John Ryan. “Platinum-Catalyzed Enantioselective Diboration of Terminal Alkenes and Vinyl Boronates: Construction of Multiborylated Compounds for Asymmetric Synthesis.” 2015. Doctoral Dissertation, Boston College. Accessed September 23, 2020. http://dlib.bc.edu/islandora/object/bc-ir:104624.

MLA Handbook (7th Edition):

Coombs, John Ryan. “Platinum-Catalyzed Enantioselective Diboration of Terminal Alkenes and Vinyl Boronates: Construction of Multiborylated Compounds for Asymmetric Synthesis.” 2015. Web. 23 Sep 2020.

Vancouver:

Coombs JR. Platinum-Catalyzed Enantioselective Diboration of Terminal Alkenes and Vinyl Boronates: Construction of Multiborylated Compounds for Asymmetric Synthesis. [Internet] [Doctoral dissertation]. Boston College; 2015. [cited 2020 Sep 23]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:104624.

Council of Science Editors:

Coombs JR. Platinum-Catalyzed Enantioselective Diboration of Terminal Alkenes and Vinyl Boronates: Construction of Multiborylated Compounds for Asymmetric Synthesis. [Doctoral Dissertation]. Boston College; 2015. Available from: http://dlib.bc.edu/islandora/object/bc-ir:104624


Universitat Rovira i Virgili

24. Alza Barrios, Esther. Approaches to asymmetric catalysis with polymer-supported pyrrolidines.

Degree: Departament de Química Analítica i Química Orgànica, 2011, Universitat Rovira i Virgili

 The present research project developed is focused in the immobilization of catalytic systems allowing the formation of carbon-carbon and carbonheteroatom bonds through enantioselective procedures with… (more)

Subjects/Keywords: Asymmetric catalysis; Organocatalysis; Supported catalysts; 54; 547

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APA (6th Edition):

Alza Barrios, E. (2011). Approaches to asymmetric catalysis with polymer-supported pyrrolidines. (Thesis). Universitat Rovira i Virgili. Retrieved from http://hdl.handle.net/10803/37362

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):

Alza Barrios, Esther. “Approaches to asymmetric catalysis with polymer-supported pyrrolidines.” 2011. Thesis, Universitat Rovira i Virgili. Accessed September 23, 2020. http://hdl.handle.net/10803/37362.

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

MLA Handbook (7th Edition):

Alza Barrios, Esther. “Approaches to asymmetric catalysis with polymer-supported pyrrolidines.” 2011. Web. 23 Sep 2020.

Vancouver:

Alza Barrios E. Approaches to asymmetric catalysis with polymer-supported pyrrolidines. [Internet] [Thesis]. Universitat Rovira i Virgili; 2011. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/10803/37362.

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

Council of Science Editors:

Alza Barrios E. Approaches to asymmetric catalysis with polymer-supported pyrrolidines. [Thesis]. Universitat Rovira i Virgili; 2011. Available from: http://hdl.handle.net/10803/37362

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


University of St Andrews

25. Belmessieri, Dorine. Applications of isothioureas in organocatalysis : kinetic resolution of secondary alcohols and intramolecular Michael addition-lactonisation.

Degree: PhD, 2013, University of St Andrews

 Obtaining enantiomerically pure compounds is of major importance in modern organic chemistry, and this PhD thesis outlines new advances made in this area. Two new… (more)

Subjects/Keywords: 541; QD505.B4; Enantioselective catalysis; asymmetric synthesis

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APA (6th Edition):

Belmessieri, D. (2013). Applications of isothioureas in organocatalysis : kinetic resolution of secondary alcohols and intramolecular Michael addition-lactonisation. (Doctoral Dissertation). University of St Andrews. Retrieved from http://hdl.handle.net/10023/4500

Chicago Manual of Style (16th Edition):

Belmessieri, Dorine. “Applications of isothioureas in organocatalysis : kinetic resolution of secondary alcohols and intramolecular Michael addition-lactonisation.” 2013. Doctoral Dissertation, University of St Andrews. Accessed September 23, 2020. http://hdl.handle.net/10023/4500.

MLA Handbook (7th Edition):

Belmessieri, Dorine. “Applications of isothioureas in organocatalysis : kinetic resolution of secondary alcohols and intramolecular Michael addition-lactonisation.” 2013. Web. 23 Sep 2020.

Vancouver:

Belmessieri D. Applications of isothioureas in organocatalysis : kinetic resolution of secondary alcohols and intramolecular Michael addition-lactonisation. [Internet] [Doctoral dissertation]. University of St Andrews; 2013. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/10023/4500.

Council of Science Editors:

Belmessieri D. Applications of isothioureas in organocatalysis : kinetic resolution of secondary alcohols and intramolecular Michael addition-lactonisation. [Doctoral Dissertation]. University of St Andrews; 2013. Available from: http://hdl.handle.net/10023/4500


National University of Ireland – Galway

26. Mc Cleary, Nadine. Design, synthesis and catalytic activity of novel oxazoline based ligands .

Degree: 2015, National University of Ireland – Galway

 This thesis can be viewed as two separate studies. Firstly, the design, synthesis and catalytic activity of novel 2-pyridyl mono(oxazoline). A family of mono(oxazoline) ligands… (more)

Subjects/Keywords: Asymmetric catalysis; Organic synthesis; School of Chemistry

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APA (6th Edition):

Mc Cleary, N. (2015). Design, synthesis and catalytic activity of novel oxazoline based ligands . (Thesis). National University of Ireland – Galway. Retrieved from http://hdl.handle.net/10379/5210

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):

Mc Cleary, Nadine. “Design, synthesis and catalytic activity of novel oxazoline based ligands .” 2015. Thesis, National University of Ireland – Galway. Accessed September 23, 2020. http://hdl.handle.net/10379/5210.

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

MLA Handbook (7th Edition):

Mc Cleary, Nadine. “Design, synthesis and catalytic activity of novel oxazoline based ligands .” 2015. Web. 23 Sep 2020.

Vancouver:

Mc Cleary N. Design, synthesis and catalytic activity of novel oxazoline based ligands . [Internet] [Thesis]. National University of Ireland – Galway; 2015. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/10379/5210.

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

Council of Science Editors:

Mc Cleary N. Design, synthesis and catalytic activity of novel oxazoline based ligands . [Thesis]. National University of Ireland – Galway; 2015. Available from: http://hdl.handle.net/10379/5210

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


National University of Ireland – Galway

27. Kellehan, David. Synthesis and Application of Chiral AraBOX ligands for Asymmetric Catalysis .

Degree: 2012, National University of Ireland – Galway

 This thesis deals with the design, synthesis and reactivity of novel 4,4'-bisoxazoline ligands and their metal complexes; (S,S)-MePrAraBOX, (S,S)-PhPrAraBOX, (S,R)-MePrAraBOX, (S,R)-PhPrAraBOX, (S,R)-BnOAcAraBOX and (S,R)-BnOHAraBOX. Metal… (more)

Subjects/Keywords: Bisoxazoline ligands; Asymmetric catalysis; Department of Chemistry

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APA (6th Edition):

Kellehan, D. (2012). Synthesis and Application of Chiral AraBOX ligands for Asymmetric Catalysis . (Thesis). National University of Ireland – Galway. Retrieved from http://hdl.handle.net/10379/3405

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):

Kellehan, David. “Synthesis and Application of Chiral AraBOX ligands for Asymmetric Catalysis .” 2012. Thesis, National University of Ireland – Galway. Accessed September 23, 2020. http://hdl.handle.net/10379/3405.

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

MLA Handbook (7th Edition):

Kellehan, David. “Synthesis and Application of Chiral AraBOX ligands for Asymmetric Catalysis .” 2012. Web. 23 Sep 2020.

Vancouver:

Kellehan D. Synthesis and Application of Chiral AraBOX ligands for Asymmetric Catalysis . [Internet] [Thesis]. National University of Ireland – Galway; 2012. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/10379/3405.

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

Council of Science Editors:

Kellehan D. Synthesis and Application of Chiral AraBOX ligands for Asymmetric Catalysis . [Thesis]. National University of Ireland – Galway; 2012. Available from: http://hdl.handle.net/10379/3405

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


Georgia State University

28. Wilkerson, Phillip D. Synthesis of Chiral N-Heterocyclic Carbene Precursors and Key Intermediates for Catalytic Enantioselective Cyclizations of Conjugated Trienes.

Degree: MS, Chemistry, 2012, Georgia State University

  Cocatalyzed reactions using Brønsted acids and chiral N-heterocyclic carbenes to yield highly enantioselective products have been reported recently in many journals. The development of… (more)

Subjects/Keywords: Asymmetric Catalysis; Catalyst Design; N-heterocyclic carbenes

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APA (6th Edition):

Wilkerson, P. D. (2012). Synthesis of Chiral N-Heterocyclic Carbene Precursors and Key Intermediates for Catalytic Enantioselective Cyclizations of Conjugated Trienes. (Thesis). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_theses/49

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):

Wilkerson, Phillip D. “Synthesis of Chiral N-Heterocyclic Carbene Precursors and Key Intermediates for Catalytic Enantioselective Cyclizations of Conjugated Trienes.” 2012. Thesis, Georgia State University. Accessed September 23, 2020. https://scholarworks.gsu.edu/chemistry_theses/49.

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

MLA Handbook (7th Edition):

Wilkerson, Phillip D. “Synthesis of Chiral N-Heterocyclic Carbene Precursors and Key Intermediates for Catalytic Enantioselective Cyclizations of Conjugated Trienes.” 2012. Web. 23 Sep 2020.

Vancouver:

Wilkerson PD. Synthesis of Chiral N-Heterocyclic Carbene Precursors and Key Intermediates for Catalytic Enantioselective Cyclizations of Conjugated Trienes. [Internet] [Thesis]. Georgia State University; 2012. [cited 2020 Sep 23]. Available from: https://scholarworks.gsu.edu/chemistry_theses/49.

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

Council of Science Editors:

Wilkerson PD. Synthesis of Chiral N-Heterocyclic Carbene Precursors and Key Intermediates for Catalytic Enantioselective Cyclizations of Conjugated Trienes. [Thesis]. Georgia State University; 2012. Available from: https://scholarworks.gsu.edu/chemistry_theses/49

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


University of Toronto

29. Smith, Samantha Alizabeth Michelle. Asymmetric Hydrogenation Using Catalysts Based on Abundant Metals.

Degree: PhD, 2018, University of Toronto

 The design of chiral catalysts for hydrogenation chemistry is a field forever continuing as there are always improvements to be made, either in activity, selectivity,… (more)

Subjects/Keywords: abundant metals; asymmetric; catalysis; hydrogenation; 0488

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

APA (6th Edition):

Smith, S. A. M. (2018). Asymmetric Hydrogenation Using Catalysts Based on Abundant Metals. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/89841

Chicago Manual of Style (16th Edition):

Smith, Samantha Alizabeth Michelle. “Asymmetric Hydrogenation Using Catalysts Based on Abundant Metals.” 2018. Doctoral Dissertation, University of Toronto. Accessed September 23, 2020. http://hdl.handle.net/1807/89841.

MLA Handbook (7th Edition):

Smith, Samantha Alizabeth Michelle. “Asymmetric Hydrogenation Using Catalysts Based on Abundant Metals.” 2018. Web. 23 Sep 2020.

Vancouver:

Smith SAM. Asymmetric Hydrogenation Using Catalysts Based on Abundant Metals. [Internet] [Doctoral dissertation]. University of Toronto; 2018. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1807/89841.

Council of Science Editors:

Smith SAM. Asymmetric Hydrogenation Using Catalysts Based on Abundant Metals. [Doctoral Dissertation]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/89841


University of Toronto

30. Kim, Byoungmoo. Asymmetric Lactone Synthesis via Hydroacylation and Stereoselective Cyclic Peptide Synthesis via Hydrogenation.

Degree: PhD, 2014, University of Toronto

Asymmetric transition metal catalysis has benefited human health by greatly facilitating access to natural products and therapeutic drugs. However, scientists continue to face challenges of… (more)

Subjects/Keywords: Asymmetric catalysis; Cyclic peptide; Lactone; Rhoidum; 0485

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

APA (6th Edition):

Kim, B. (2014). Asymmetric Lactone Synthesis via Hydroacylation and Stereoselective Cyclic Peptide Synthesis via Hydrogenation. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/71059

Chicago Manual of Style (16th Edition):

Kim, Byoungmoo. “Asymmetric Lactone Synthesis via Hydroacylation and Stereoselective Cyclic Peptide Synthesis via Hydrogenation.” 2014. Doctoral Dissertation, University of Toronto. Accessed September 23, 2020. http://hdl.handle.net/1807/71059.

MLA Handbook (7th Edition):

Kim, Byoungmoo. “Asymmetric Lactone Synthesis via Hydroacylation and Stereoselective Cyclic Peptide Synthesis via Hydrogenation.” 2014. Web. 23 Sep 2020.

Vancouver:

Kim B. Asymmetric Lactone Synthesis via Hydroacylation and Stereoselective Cyclic Peptide Synthesis via Hydrogenation. [Internet] [Doctoral dissertation]. University of Toronto; 2014. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1807/71059.

Council of Science Editors:

Kim B. Asymmetric Lactone Synthesis via Hydroacylation and Stereoselective Cyclic Peptide Synthesis via Hydrogenation. [Doctoral Dissertation]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/71059

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