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You searched for subject:(Organocatalysis). Showing records 1 – 30 of 330 total matches.

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1. Davis, Lindsey Oliver. DEVELOPMENT OF METAL-CATALYZED REACTIONS OF ALLENES WITH IMINES AND THE INVESTIGATION OF BRΘNSTED ACID CATALYZED ENE REACTIONS.

Degree: 2009, Wake Forest University

 Since the birth of organic chemistry in the 19th century, scientists have been discovering new reactions to generate interesting synthetic targets. As these new reactions… (more)

Subjects/Keywords: organocatalysis

organocatalysis reactions.33 Brønsted acids can catalyze reactions by two possible mechanisms: specific… …enzymatic reactions, and it is highly likely these exist in organocatalysis. This aspect of… …organocatalysis is fascinating, and is an unexplored area. Understanding the general catalysis… …nature and the design of Brønsted acids for organocatalysis. Hydrogen-bonding interactions… …their design multifunctional organocatalysts. 1.3.4 Small molecule organocatalysis The… 

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APA (6th Edition):

Davis, L. O. (2009). DEVELOPMENT OF METAL-CATALYZED REACTIONS OF ALLENES WITH IMINES AND THE INVESTIGATION OF BRΘNSTED ACID CATALYZED ENE REACTIONS. (Thesis). Wake Forest University. Retrieved from http://hdl.handle.net/10339/14680

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):

Davis, Lindsey Oliver. “DEVELOPMENT OF METAL-CATALYZED REACTIONS OF ALLENES WITH IMINES AND THE INVESTIGATION OF BRΘNSTED ACID CATALYZED ENE REACTIONS.” 2009. Thesis, Wake Forest University. Accessed April 22, 2021. http://hdl.handle.net/10339/14680.

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

MLA Handbook (7th Edition):

Davis, Lindsey Oliver. “DEVELOPMENT OF METAL-CATALYZED REACTIONS OF ALLENES WITH IMINES AND THE INVESTIGATION OF BRΘNSTED ACID CATALYZED ENE REACTIONS.” 2009. Web. 22 Apr 2021.

Vancouver:

Davis LO. DEVELOPMENT OF METAL-CATALYZED REACTIONS OF ALLENES WITH IMINES AND THE INVESTIGATION OF BRΘNSTED ACID CATALYZED ENE REACTIONS. [Internet] [Thesis]. Wake Forest University; 2009. [cited 2021 Apr 22]. Available from: http://hdl.handle.net/10339/14680.

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

Council of Science Editors:

Davis LO. DEVELOPMENT OF METAL-CATALYZED REACTIONS OF ALLENES WITH IMINES AND THE INVESTIGATION OF BRΘNSTED ACID CATALYZED ENE REACTIONS. [Thesis]. Wake Forest University; 2009. Available from: http://hdl.handle.net/10339/14680

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


University of Oxford

2. Farley, Alistair J. M. Development and application of a new class of potent bifunctional organocatalysts.

Degree: PhD, 2015, University of Oxford

 This thesis describes the development and application of a new class of bifunctional organocatalysts, incorporating the novel triaryliminophosphorane organosuperbases, for asymmetric synthesis. This thesis seeks… (more)

Subjects/Keywords: 547; organocatalysis

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APA (6th Edition):

Farley, A. J. M. (2015). Development and application of a new class of potent bifunctional organocatalysts. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:08599f4b-3c8e-46f8-858a-0340c769e904 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.711954

Chicago Manual of Style (16th Edition):

Farley, Alistair J M. “Development and application of a new class of potent bifunctional organocatalysts.” 2015. Doctoral Dissertation, University of Oxford. Accessed April 22, 2021. http://ora.ox.ac.uk/objects/uuid:08599f4b-3c8e-46f8-858a-0340c769e904 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.711954.

MLA Handbook (7th Edition):

Farley, Alistair J M. “Development and application of a new class of potent bifunctional organocatalysts.” 2015. Web. 22 Apr 2021.

Vancouver:

Farley AJM. Development and application of a new class of potent bifunctional organocatalysts. [Internet] [Doctoral dissertation]. University of Oxford; 2015. [cited 2021 Apr 22]. Available from: http://ora.ox.ac.uk/objects/uuid:08599f4b-3c8e-46f8-858a-0340c769e904 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.711954.

Council of Science Editors:

Farley AJM. Development and application of a new class of potent bifunctional organocatalysts. [Doctoral Dissertation]. University of Oxford; 2015. Available from: http://ora.ox.ac.uk/objects/uuid:08599f4b-3c8e-46f8-858a-0340c769e904 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.711954


University of Bath

3. Taylor, James Edward. New applications of organocatalysis.

Degree: PhD, 2011, University of Bath

 New applications of organocatalysis, in particular the use of the bicyclic amidine DBN (1,5-diazabicyclo[4.3.0]non-5-ene) and then iodide as nucleophilic catalysts for Friedel-Crafts reactions, have been… (more)

Subjects/Keywords: 541.39; organocatalysis

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APA (6th Edition):

Taylor, J. E. (2011). New applications of organocatalysis. (Doctoral Dissertation). University of Bath. Retrieved from https://researchportal.bath.ac.uk/en/studentthesis/new-applications-of-organocatalysis(65defed5-1557-4940-bf97-84441d68490c).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.547629

Chicago Manual of Style (16th Edition):

Taylor, James Edward. “New applications of organocatalysis.” 2011. Doctoral Dissertation, University of Bath. Accessed April 22, 2021. https://researchportal.bath.ac.uk/en/studentthesis/new-applications-of-organocatalysis(65defed5-1557-4940-bf97-84441d68490c).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.547629.

MLA Handbook (7th Edition):

Taylor, James Edward. “New applications of organocatalysis.” 2011. Web. 22 Apr 2021.

Vancouver:

Taylor JE. New applications of organocatalysis. [Internet] [Doctoral dissertation]. University of Bath; 2011. [cited 2021 Apr 22]. Available from: https://researchportal.bath.ac.uk/en/studentthesis/new-applications-of-organocatalysis(65defed5-1557-4940-bf97-84441d68490c).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.547629.

Council of Science Editors:

Taylor JE. New applications of organocatalysis. [Doctoral Dissertation]. University of Bath; 2011. Available from: https://researchportal.bath.ac.uk/en/studentthesis/new-applications-of-organocatalysis(65defed5-1557-4940-bf97-84441d68490c).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.547629


Oregon State University

4. Johnston, Ryne Connell. Rationalization and innovative design of asymmetric organocatalysts through computational investigation.

Degree: PhD, Chemistry, 2015, Oregon State University

 My work on computing complex catalyzed organic transformations reveals that only a few subtle chemical factors, e.g. non-classical hydrogen bonding, (hyper)conjugation and steric effects, common… (more)

Subjects/Keywords: organocatalysis; Catalysts  – Design

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APA (6th Edition):

Johnston, R. C. (2015). Rationalization and innovative design of asymmetric organocatalysts through computational investigation. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/55470

Chicago Manual of Style (16th Edition):

Johnston, Ryne Connell. “Rationalization and innovative design of asymmetric organocatalysts through computational investigation.” 2015. Doctoral Dissertation, Oregon State University. Accessed April 22, 2021. http://hdl.handle.net/1957/55470.

MLA Handbook (7th Edition):

Johnston, Ryne Connell. “Rationalization and innovative design of asymmetric organocatalysts through computational investigation.” 2015. Web. 22 Apr 2021.

Vancouver:

Johnston RC. Rationalization and innovative design of asymmetric organocatalysts through computational investigation. [Internet] [Doctoral dissertation]. Oregon State University; 2015. [cited 2021 Apr 22]. Available from: http://hdl.handle.net/1957/55470.

Council of Science Editors:

Johnston RC. Rationalization and innovative design of asymmetric organocatalysts through computational investigation. [Doctoral Dissertation]. Oregon State University; 2015. Available from: http://hdl.handle.net/1957/55470


University of Michigan

5. Winschel, Grace A. Chiral Phosphoric Acid-Catalyzed Stereoselective Transformations of Vinyl Ethers and Acetals.

Degree: PhD, Chemistry, 2015, University of Michigan

 Few methods exist for asymmetric nucleophilic addition to reactive oxocarbenia-like systems. A direct, chiral-catalyst controlled method to perform such transformations would simplify the task of… (more)

Subjects/Keywords: oxocarbenia; asymmetric organocatalysis; Chemistry; Science

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APA (6th Edition):

Winschel, G. A. (2015). Chiral Phosphoric Acid-Catalyzed Stereoselective Transformations of Vinyl Ethers and Acetals. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/113427

Chicago Manual of Style (16th Edition):

Winschel, Grace A. “Chiral Phosphoric Acid-Catalyzed Stereoselective Transformations of Vinyl Ethers and Acetals.” 2015. Doctoral Dissertation, University of Michigan. Accessed April 22, 2021. http://hdl.handle.net/2027.42/113427.

MLA Handbook (7th Edition):

Winschel, Grace A. “Chiral Phosphoric Acid-Catalyzed Stereoselective Transformations of Vinyl Ethers and Acetals.” 2015. Web. 22 Apr 2021.

Vancouver:

Winschel GA. Chiral Phosphoric Acid-Catalyzed Stereoselective Transformations of Vinyl Ethers and Acetals. [Internet] [Doctoral dissertation]. University of Michigan; 2015. [cited 2021 Apr 22]. Available from: http://hdl.handle.net/2027.42/113427.

Council of Science Editors:

Winschel GA. Chiral Phosphoric Acid-Catalyzed Stereoselective Transformations of Vinyl Ethers and Acetals. [Doctoral Dissertation]. University of Michigan; 2015. Available from: http://hdl.handle.net/2027.42/113427


Texas A&M University

6. Abbasov, Mikail Eminovich. Diels–Alder–Initiated Organocascades Employing Acylammonium Catalysis: Scope, Mechanism, and Application.

Degree: PhD, Chemistry, 2015, Texas A&M University

 Following the turn of the millennium, the role of asymmetric covalent organocatalysis has developed into a scalable, synthetic paradigm galvanizing the synthetic community toward utilization… (more)

Subjects/Keywords: Diels–Alder; Organocatalysis; Organocascade; Acylammonium

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APA (6th Edition):

Abbasov, M. E. (2015). Diels–Alder–Initiated Organocascades Employing Acylammonium Catalysis: Scope, Mechanism, and Application. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/187468

Chicago Manual of Style (16th Edition):

Abbasov, Mikail Eminovich. “Diels–Alder–Initiated Organocascades Employing Acylammonium Catalysis: Scope, Mechanism, and Application.” 2015. Doctoral Dissertation, Texas A&M University. Accessed April 22, 2021. http://hdl.handle.net/1969.1/187468.

MLA Handbook (7th Edition):

Abbasov, Mikail Eminovich. “Diels–Alder–Initiated Organocascades Employing Acylammonium Catalysis: Scope, Mechanism, and Application.” 2015. Web. 22 Apr 2021.

Vancouver:

Abbasov ME. Diels–Alder–Initiated Organocascades Employing Acylammonium Catalysis: Scope, Mechanism, and Application. [Internet] [Doctoral dissertation]. Texas A&M University; 2015. [cited 2021 Apr 22]. Available from: http://hdl.handle.net/1969.1/187468.

Council of Science Editors:

Abbasov ME. Diels–Alder–Initiated Organocascades Employing Acylammonium Catalysis: Scope, Mechanism, and Application. [Doctoral Dissertation]. Texas A&M University; 2015. Available from: http://hdl.handle.net/1969.1/187468


Texas A&M University

7. Khamatnurova, Tatyana. Phase Selectively Soluble Polystyrene-Supported Organocatalysts.

Degree: PhD, Chemistry, 2014, Texas A&M University

 Alkane phase selectively soluble poly(4-alkylstyrene) supports have been developed. 4-Methyl-, 4-tert-butyl, 4-dodecyl-, and 4-octadecylstyrene were copolymerized with 5-10 mol % of 4-chloromethylstyrene to afford co-… (more)

Subjects/Keywords: Polystyrene; Phase Selective Solubility; Organocatalysis

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APA (6th Edition):

Khamatnurova, T. (2014). Phase Selectively Soluble Polystyrene-Supported Organocatalysts. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/153374

Chicago Manual of Style (16th Edition):

Khamatnurova, Tatyana. “Phase Selectively Soluble Polystyrene-Supported Organocatalysts.” 2014. Doctoral Dissertation, Texas A&M University. Accessed April 22, 2021. http://hdl.handle.net/1969.1/153374.

MLA Handbook (7th Edition):

Khamatnurova, Tatyana. “Phase Selectively Soluble Polystyrene-Supported Organocatalysts.” 2014. Web. 22 Apr 2021.

Vancouver:

Khamatnurova T. Phase Selectively Soluble Polystyrene-Supported Organocatalysts. [Internet] [Doctoral dissertation]. Texas A&M University; 2014. [cited 2021 Apr 22]. Available from: http://hdl.handle.net/1969.1/153374.

Council of Science Editors:

Khamatnurova T. Phase Selectively Soluble Polystyrene-Supported Organocatalysts. [Doctoral Dissertation]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/153374

8. Nielsen, Alexander J. Novel Wittig and Organocatalytic Methodologies for the Synthesis of Chemotherapeutic Compounds.

Degree: PhD, 2019, McMaster University

This thesis is primarily focused on the development of Wittig methodologies and the applications of the product alkenes in organocatalysis and drug discovery. Herein is… (more)

Subjects/Keywords: Wittig; organocatalysis; chemotherapeutics; anticancer; antiviral

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APA (6th Edition):

Nielsen, A. J. (2019). Novel Wittig and Organocatalytic Methodologies for the Synthesis of Chemotherapeutic Compounds. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/24463

Chicago Manual of Style (16th Edition):

Nielsen, Alexander J. “Novel Wittig and Organocatalytic Methodologies for the Synthesis of Chemotherapeutic Compounds.” 2019. Doctoral Dissertation, McMaster University. Accessed April 22, 2021. http://hdl.handle.net/11375/24463.

MLA Handbook (7th Edition):

Nielsen, Alexander J. “Novel Wittig and Organocatalytic Methodologies for the Synthesis of Chemotherapeutic Compounds.” 2019. Web. 22 Apr 2021.

Vancouver:

Nielsen AJ. Novel Wittig and Organocatalytic Methodologies for the Synthesis of Chemotherapeutic Compounds. [Internet] [Doctoral dissertation]. McMaster University; 2019. [cited 2021 Apr 22]. Available from: http://hdl.handle.net/11375/24463.

Council of Science Editors:

Nielsen AJ. Novel Wittig and Organocatalytic Methodologies for the Synthesis of Chemotherapeutic Compounds. [Doctoral Dissertation]. McMaster University; 2019. Available from: http://hdl.handle.net/11375/24463


McMaster University

9. Zepeda-Velazquez, Carlos Armando. DEVELOPMENT OF AN ORGANOCATALYTIC [3+3] REACTION SEQUENCE TOWARD AMINOCYCLITOLS AND TOTAL SYNTHESIS OF ANTICANCER AMARYLLIDACEAE ALKALOIDS.

Degree: PhD, 2015, McMaster University

In the thesis, the development of asymmetric organocatalytic [3+3] sequences for the assembly of aminocyclitols is described. A water-based Wittig reaction was developed in order… (more)

Subjects/Keywords: Organocatalysis; (+)-trans-dihydrolycoricidine; Natural product

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APA (6th Edition):

Zepeda-Velazquez, C. A. (2015). DEVELOPMENT OF AN ORGANOCATALYTIC [3+3] REACTION SEQUENCE TOWARD AMINOCYCLITOLS AND TOTAL SYNTHESIS OF ANTICANCER AMARYLLIDACEAE ALKALOIDS. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/18192

Chicago Manual of Style (16th Edition):

Zepeda-Velazquez, Carlos Armando. “DEVELOPMENT OF AN ORGANOCATALYTIC [3+3] REACTION SEQUENCE TOWARD AMINOCYCLITOLS AND TOTAL SYNTHESIS OF ANTICANCER AMARYLLIDACEAE ALKALOIDS.” 2015. Doctoral Dissertation, McMaster University. Accessed April 22, 2021. http://hdl.handle.net/11375/18192.

MLA Handbook (7th Edition):

Zepeda-Velazquez, Carlos Armando. “DEVELOPMENT OF AN ORGANOCATALYTIC [3+3] REACTION SEQUENCE TOWARD AMINOCYCLITOLS AND TOTAL SYNTHESIS OF ANTICANCER AMARYLLIDACEAE ALKALOIDS.” 2015. Web. 22 Apr 2021.

Vancouver:

Zepeda-Velazquez CA. DEVELOPMENT OF AN ORGANOCATALYTIC [3+3] REACTION SEQUENCE TOWARD AMINOCYCLITOLS AND TOTAL SYNTHESIS OF ANTICANCER AMARYLLIDACEAE ALKALOIDS. [Internet] [Doctoral dissertation]. McMaster University; 2015. [cited 2021 Apr 22]. Available from: http://hdl.handle.net/11375/18192.

Council of Science Editors:

Zepeda-Velazquez CA. DEVELOPMENT OF AN ORGANOCATALYTIC [3+3] REACTION SEQUENCE TOWARD AMINOCYCLITOLS AND TOTAL SYNTHESIS OF ANTICANCER AMARYLLIDACEAE ALKALOIDS. [Doctoral Dissertation]. McMaster University; 2015. Available from: http://hdl.handle.net/11375/18192


University of Houston

10. Vallakati, Ravikrishna 1977-. Synthesis of the Antimalarial Flindersial Alkaloids.

Degree: PhD, Chemistry, 2015, University of Houston

 The concept of mimicking nature to synthesize natural compounds has been successfully demonstrated in the synthesis of all the anti-malarial Flindersia alkaloids. Previous work on… (more)

Subjects/Keywords: Flinderoles; antimalarial; Biomimetic Synthesis; Organocatalysis

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APA (6th Edition):

Vallakati, R. 1. (2015). Synthesis of the Antimalarial Flindersial Alkaloids. (Doctoral Dissertation). University of Houston. Retrieved from http://hdl.handle.net/10657/6552

Chicago Manual of Style (16th Edition):

Vallakati, Ravikrishna 1977-. “Synthesis of the Antimalarial Flindersial Alkaloids.” 2015. Doctoral Dissertation, University of Houston. Accessed April 22, 2021. http://hdl.handle.net/10657/6552.

MLA Handbook (7th Edition):

Vallakati, Ravikrishna 1977-. “Synthesis of the Antimalarial Flindersial Alkaloids.” 2015. Web. 22 Apr 2021.

Vancouver:

Vallakati R1. Synthesis of the Antimalarial Flindersial Alkaloids. [Internet] [Doctoral dissertation]. University of Houston; 2015. [cited 2021 Apr 22]. Available from: http://hdl.handle.net/10657/6552.

Council of Science Editors:

Vallakati R1. Synthesis of the Antimalarial Flindersial Alkaloids. [Doctoral Dissertation]. University of Houston; 2015. Available from: http://hdl.handle.net/10657/6552

11. CRONIN, SARAH. Practical and enantioselective amino acid synthesis via novel catalytic ring opening processes.

Degree: School of Chemistry. Discipline of Chemistry, 2019, Trinity College Dublin

 A novel methodology for the kinetic resolution (KR) of tetrachloroisopropoxycarbonyl (TCIC) substituted oxazinones via alcoholysis to afford enantioenriched and orthogonally protected ?-amino acids has been… (more)

Subjects/Keywords: Chemistry; organocatalysis; kinetic resolution

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APA (6th Edition):

CRONIN, S. (2019). Practical and enantioselective amino acid synthesis via novel catalytic ring opening processes. (Thesis). Trinity College Dublin. Retrieved from http://hdl.handle.net/2262/86152

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):

CRONIN, SARAH. “Practical and enantioselective amino acid synthesis via novel catalytic ring opening processes.” 2019. Thesis, Trinity College Dublin. Accessed April 22, 2021. http://hdl.handle.net/2262/86152.

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

MLA Handbook (7th Edition):

CRONIN, SARAH. “Practical and enantioselective amino acid synthesis via novel catalytic ring opening processes.” 2019. Web. 22 Apr 2021.

Vancouver:

CRONIN S. Practical and enantioselective amino acid synthesis via novel catalytic ring opening processes. [Internet] [Thesis]. Trinity College Dublin; 2019. [cited 2021 Apr 22]. Available from: http://hdl.handle.net/2262/86152.

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

Council of Science Editors:

CRONIN S. Practical and enantioselective amino acid synthesis via novel catalytic ring opening processes. [Thesis]. Trinity College Dublin; 2019. Available from: http://hdl.handle.net/2262/86152

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


University of Illinois – Urbana-Champaign

12. Kornfilt, David Jean Pierre. Lewis base catalyzed enantioselective oxysulfenylation of alkenes.

Degree: PhD, Chemistry, 2016, University of Illinois – Urbana-Champaign

 The Lewis base activation of Lewis acids has been harnessed in the development of an enantioselective oxysulfenylation reaction for unactivated alkenes. The weak Lewis acid… (more)

Subjects/Keywords: Catalysis; Lewis Bases; Enantioselecive; Organocatalysis

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APA (6th Edition):

Kornfilt, D. J. P. (2016). Lewis base catalyzed enantioselective oxysulfenylation of alkenes. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/95493

Chicago Manual of Style (16th Edition):

Kornfilt, David Jean Pierre. “Lewis base catalyzed enantioselective oxysulfenylation of alkenes.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed April 22, 2021. http://hdl.handle.net/2142/95493.

MLA Handbook (7th Edition):

Kornfilt, David Jean Pierre. “Lewis base catalyzed enantioselective oxysulfenylation of alkenes.” 2016. Web. 22 Apr 2021.

Vancouver:

Kornfilt DJP. Lewis base catalyzed enantioselective oxysulfenylation of alkenes. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2021 Apr 22]. Available from: http://hdl.handle.net/2142/95493.

Council of Science Editors:

Kornfilt DJP. Lewis base catalyzed enantioselective oxysulfenylation of alkenes. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/95493


University of New Mexico

13. Zhang, Xinshuai. Alkynal involved organocatalytic reactions.

Degree: Department of Chemistry and Chemical Biology, 2012, University of New Mexico

 During the past twenty years, vast progress has been achieved in the field of organocatalysis. One of the fruitful areas is iminium catalysis using α,… (more)

Subjects/Keywords: alkynal; Organocatalysis; Iminium-Allenamine

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APA (6th Edition):

Zhang, X. (2012). Alkynal involved organocatalytic reactions. (Doctoral Dissertation). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/chem_etds/27

Chicago Manual of Style (16th Edition):

Zhang, Xinshuai. “Alkynal involved organocatalytic reactions.” 2012. Doctoral Dissertation, University of New Mexico. Accessed April 22, 2021. https://digitalrepository.unm.edu/chem_etds/27.

MLA Handbook (7th Edition):

Zhang, Xinshuai. “Alkynal involved organocatalytic reactions.” 2012. Web. 22 Apr 2021.

Vancouver:

Zhang X. Alkynal involved organocatalytic reactions. [Internet] [Doctoral dissertation]. University of New Mexico; 2012. [cited 2021 Apr 22]. Available from: https://digitalrepository.unm.edu/chem_etds/27.

Council of Science Editors:

Zhang X. Alkynal involved organocatalytic reactions. [Doctoral Dissertation]. University of New Mexico; 2012. Available from: https://digitalrepository.unm.edu/chem_etds/27


Georgia Tech

14. Bakr, Brandon Wallace. Symmetry-adapted perturbation theory for organocatalysis.

Degree: PhD, Chemistry and Biochemistry, 2018, Georgia Tech

 Functional-group and atomic partitions of symmetry-adapted perturbation theory (SAPT) were used, for the first time, to analyze non-covalent interactions thought to influence the selectivity of… (more)

Subjects/Keywords: Symmetry-adapted perturbation theory; Organocatalysis

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APA (6th Edition):

Bakr, B. W. (2018). Symmetry-adapted perturbation theory for organocatalysis. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/60207

Chicago Manual of Style (16th Edition):

Bakr, Brandon Wallace. “Symmetry-adapted perturbation theory for organocatalysis.” 2018. Doctoral Dissertation, Georgia Tech. Accessed April 22, 2021. http://hdl.handle.net/1853/60207.

MLA Handbook (7th Edition):

Bakr, Brandon Wallace. “Symmetry-adapted perturbation theory for organocatalysis.” 2018. Web. 22 Apr 2021.

Vancouver:

Bakr BW. Symmetry-adapted perturbation theory for organocatalysis. [Internet] [Doctoral dissertation]. Georgia Tech; 2018. [cited 2021 Apr 22]. Available from: http://hdl.handle.net/1853/60207.

Council of Science Editors:

Bakr BW. Symmetry-adapted perturbation theory for organocatalysis. [Doctoral Dissertation]. Georgia Tech; 2018. Available from: http://hdl.handle.net/1853/60207


University of Kansas

15. Haugeberg, Benjamin John. Development and Application of Quinone-Catalyzed C-C Bond Cleavage.

Degree: MS, Chemistry, 2016, University of Kansas

Organocatalysis is a synthetic field of ever increasing development and utility. Of the reactions and small molecule catalysts developed over the last 20 years, a… (more)

Subjects/Keywords: Chemistry; Homologation; Organocatalysis; Quinone

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APA (6th Edition):

Haugeberg, B. J. (2016). Development and Application of Quinone-Catalyzed C-C Bond Cleavage. (Masters Thesis). University of Kansas. Retrieved from http://hdl.handle.net/1808/25765

Chicago Manual of Style (16th Edition):

Haugeberg, Benjamin John. “Development and Application of Quinone-Catalyzed C-C Bond Cleavage.” 2016. Masters Thesis, University of Kansas. Accessed April 22, 2021. http://hdl.handle.net/1808/25765.

MLA Handbook (7th Edition):

Haugeberg, Benjamin John. “Development and Application of Quinone-Catalyzed C-C Bond Cleavage.” 2016. Web. 22 Apr 2021.

Vancouver:

Haugeberg BJ. Development and Application of Quinone-Catalyzed C-C Bond Cleavage. [Internet] [Masters thesis]. University of Kansas; 2016. [cited 2021 Apr 22]. Available from: http://hdl.handle.net/1808/25765.

Council of Science Editors:

Haugeberg BJ. Development and Application of Quinone-Catalyzed C-C Bond Cleavage. [Masters Thesis]. University of Kansas; 2016. Available from: http://hdl.handle.net/1808/25765


University of Canterbury

16. Singh, Govind Pratap. New approaches to stereocontrolled glycosylation.

Degree: PhD, Chemistry, 2015, University of Canterbury

 The conceptually simple process of linking carbohydrate units by glycosylation has proven to be one of the most difficult synthetic processes to control from a… (more)

Subjects/Keywords: carbohydrate; glycosylation; stereoselective; NGP; organocatalysis

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APA (6th Edition):

Singh, G. P. (2015). New approaches to stereocontrolled glycosylation. (Doctoral Dissertation). University of Canterbury. Retrieved from http://dx.doi.org/10.26021/6577

Chicago Manual of Style (16th Edition):

Singh, Govind Pratap. “New approaches to stereocontrolled glycosylation.” 2015. Doctoral Dissertation, University of Canterbury. Accessed April 22, 2021. http://dx.doi.org/10.26021/6577.

MLA Handbook (7th Edition):

Singh, Govind Pratap. “New approaches to stereocontrolled glycosylation.” 2015. Web. 22 Apr 2021.

Vancouver:

Singh GP. New approaches to stereocontrolled glycosylation. [Internet] [Doctoral dissertation]. University of Canterbury; 2015. [cited 2021 Apr 22]. Available from: http://dx.doi.org/10.26021/6577.

Council of Science Editors:

Singh GP. New approaches to stereocontrolled glycosylation. [Doctoral Dissertation]. University of Canterbury; 2015. Available from: http://dx.doi.org/10.26021/6577


University of St. Andrews

17. Wu, Jiufeng. Probing the reactivity of α,β-unsaturated acyl ammonium intermediates in organocatalysis.

Degree: 2020, University of St. Andrews

 The research described in this thesis focuses on probing the reactivity of α,β-unsaturated acyl ammonium intermediates and the use of theses reactive intermediates in a… (more)

Subjects/Keywords: Organocatalysis; Acyl ammonium intermediates

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APA (6th Edition):

Wu, J. (2020). Probing the reactivity of α,β-unsaturated acyl ammonium intermediates in organocatalysis. (Doctoral Dissertation). University of St. Andrews. Retrieved from http://hdl.handle.net/10023/20181

Chicago Manual of Style (16th Edition):

Wu, Jiufeng. “Probing the reactivity of α,β-unsaturated acyl ammonium intermediates in organocatalysis.” 2020. Doctoral Dissertation, University of St. Andrews. Accessed April 22, 2021. http://hdl.handle.net/10023/20181.

MLA Handbook (7th Edition):

Wu, Jiufeng. “Probing the reactivity of α,β-unsaturated acyl ammonium intermediates in organocatalysis.” 2020. Web. 22 Apr 2021.

Vancouver:

Wu J. Probing the reactivity of α,β-unsaturated acyl ammonium intermediates in organocatalysis. [Internet] [Doctoral dissertation]. University of St. Andrews; 2020. [cited 2021 Apr 22]. Available from: http://hdl.handle.net/10023/20181.

Council of Science Editors:

Wu J. Probing the reactivity of α,β-unsaturated acyl ammonium intermediates in organocatalysis. [Doctoral Dissertation]. University of St. Andrews; 2020. Available from: http://hdl.handle.net/10023/20181


University of California – Berkeley

18. 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 April 22, 2021. 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. 22 Apr 2021.

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 2021 Apr 22]. 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 Rochester

19. Biegasiewicz, Kyle Francis (1988 - ). Part I. Mechanistic studies, optimization, and further applications of the organocatalytic α -hydroxymethylation of aldehydes ; Part II. Studies toward the total synthesis of FK-506.

Degree: PhD, 2017, University of Rochester

 Part I. Mechanistic Studies, Optimization, and Further Applications of the Organocatalytic α -Hydroxymethylation of Aldehydes: </br> Further developments in studies of the direct α-hydroymethylation of… (more)

Subjects/Keywords: FK-506; Hydroxymethylation; Organocatalysis; Total synthesis

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APA (6th Edition):

Biegasiewicz, K. F. (. -. ). (2017). Part I. Mechanistic studies, optimization, and further applications of the organocatalytic α -hydroxymethylation of aldehydes ; Part II. Studies toward the total synthesis of FK-506. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/31893

Chicago Manual of Style (16th Edition):

Biegasiewicz, Kyle Francis (1988 - ). “Part I. Mechanistic studies, optimization, and further applications of the organocatalytic α -hydroxymethylation of aldehydes ; Part II. Studies toward the total synthesis of FK-506.” 2017. Doctoral Dissertation, University of Rochester. Accessed April 22, 2021. http://hdl.handle.net/1802/31893.

MLA Handbook (7th Edition):

Biegasiewicz, Kyle Francis (1988 - ). “Part I. Mechanistic studies, optimization, and further applications of the organocatalytic α -hydroxymethylation of aldehydes ; Part II. Studies toward the total synthesis of FK-506.” 2017. Web. 22 Apr 2021.

Vancouver:

Biegasiewicz KF(-). Part I. Mechanistic studies, optimization, and further applications of the organocatalytic α -hydroxymethylation of aldehydes ; Part II. Studies toward the total synthesis of FK-506. [Internet] [Doctoral dissertation]. University of Rochester; 2017. [cited 2021 Apr 22]. Available from: http://hdl.handle.net/1802/31893.

Council of Science Editors:

Biegasiewicz KF(-). Part I. Mechanistic studies, optimization, and further applications of the organocatalytic α -hydroxymethylation of aldehydes ; Part II. Studies toward the total synthesis of FK-506. [Doctoral Dissertation]. University of Rochester; 2017. Available from: http://hdl.handle.net/1802/31893


Cornell University

20. Opalka, Suzanne. Development Of Catalytic Systems In Batch And Flow Using Dual Organocatalysts And Solid Packed-Bed Reactors.

Degree: PhD, Chemistry and Chemical Biology, 2012, Cornell University

 This dissertation discusses the development of complex catalytic systems in both batch and flow reactors using either organocatalysts or transition metal complexes with the future… (more)

Subjects/Keywords: Continuous-flow chemistry; Organocatalysis; packed-bed microreactor

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APA (6th Edition):

Opalka, S. (2012). Development Of Catalytic Systems In Batch And Flow Using Dual Organocatalysts And Solid Packed-Bed Reactors. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/31490

Chicago Manual of Style (16th Edition):

Opalka, Suzanne. “Development Of Catalytic Systems In Batch And Flow Using Dual Organocatalysts And Solid Packed-Bed Reactors.” 2012. Doctoral Dissertation, Cornell University. Accessed April 22, 2021. http://hdl.handle.net/1813/31490.

MLA Handbook (7th Edition):

Opalka, Suzanne. “Development Of Catalytic Systems In Batch And Flow Using Dual Organocatalysts And Solid Packed-Bed Reactors.” 2012. Web. 22 Apr 2021.

Vancouver:

Opalka S. Development Of Catalytic Systems In Batch And Flow Using Dual Organocatalysts And Solid Packed-Bed Reactors. [Internet] [Doctoral dissertation]. Cornell University; 2012. [cited 2021 Apr 22]. Available from: http://hdl.handle.net/1813/31490.

Council of Science Editors:

Opalka S. Development Of Catalytic Systems In Batch And Flow Using Dual Organocatalysts And Solid Packed-Bed Reactors. [Doctoral Dissertation]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/31490


Vanderbilt University

21. Vara, Brandon Anthony. Enantioselective Reaction Development using Chiral Bifunctional Brønsted Acid/Base Organocatalysis and Applications to Target Molecule Synthesis.

Degree: PhD, Chemistry, 2015, Vanderbilt University

 The Nutlin class of cis-imidazoline small molecule therapeutics has been shown to inhibit the protein-protein interaction (PPI) between the tumor-suppressor protein p53 and MDM2. The… (more)

Subjects/Keywords: organocatalysis; catalysis; Nutlin; organic; Fluorine; Carbon Dioxide

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APA (6th Edition):

Vara, B. A. (2015). Enantioselective Reaction Development using Chiral Bifunctional Brønsted Acid/Base Organocatalysis and Applications to Target Molecule Synthesis. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/15220

Chicago Manual of Style (16th Edition):

Vara, Brandon Anthony. “Enantioselective Reaction Development using Chiral Bifunctional Brønsted Acid/Base Organocatalysis and Applications to Target Molecule Synthesis.” 2015. Doctoral Dissertation, Vanderbilt University. Accessed April 22, 2021. http://hdl.handle.net/1803/15220.

MLA Handbook (7th Edition):

Vara, Brandon Anthony. “Enantioselective Reaction Development using Chiral Bifunctional Brønsted Acid/Base Organocatalysis and Applications to Target Molecule Synthesis.” 2015. Web. 22 Apr 2021.

Vancouver:

Vara BA. Enantioselective Reaction Development using Chiral Bifunctional Brønsted Acid/Base Organocatalysis and Applications to Target Molecule Synthesis. [Internet] [Doctoral dissertation]. Vanderbilt University; 2015. [cited 2021 Apr 22]. Available from: http://hdl.handle.net/1803/15220.

Council of Science Editors:

Vara BA. Enantioselective Reaction Development using Chiral Bifunctional Brønsted Acid/Base Organocatalysis and Applications to Target Molecule Synthesis. [Doctoral Dissertation]. Vanderbilt University; 2015. Available from: http://hdl.handle.net/1803/15220


Texas A&M University

22. Sepulveda Camarena, Diana. Computational Chemistry as a Tool for Understanding Non-Covalent Interactions in Organic Reactions and Materials.

Degree: PhD, Chemistry, 2014, Texas A&M University

 Non-covalent interactions (NCIs) play vital roles in many areas of chemistry and materials science. Although there has been a great deal of progress understanding the… (more)

Subjects/Keywords: Organic Chemistry; c-HBC; organocatalysis; computational chemistry

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APA (6th Edition):

Sepulveda Camarena, D. (2014). Computational Chemistry as a Tool for Understanding Non-Covalent Interactions in Organic Reactions and Materials. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/154033

Chicago Manual of Style (16th Edition):

Sepulveda Camarena, Diana. “Computational Chemistry as a Tool for Understanding Non-Covalent Interactions in Organic Reactions and Materials.” 2014. Doctoral Dissertation, Texas A&M University. Accessed April 22, 2021. http://hdl.handle.net/1969.1/154033.

MLA Handbook (7th Edition):

Sepulveda Camarena, Diana. “Computational Chemistry as a Tool for Understanding Non-Covalent Interactions in Organic Reactions and Materials.” 2014. Web. 22 Apr 2021.

Vancouver:

Sepulveda Camarena D. Computational Chemistry as a Tool for Understanding Non-Covalent Interactions in Organic Reactions and Materials. [Internet] [Doctoral dissertation]. Texas A&M University; 2014. [cited 2021 Apr 22]. Available from: http://hdl.handle.net/1969.1/154033.

Council of Science Editors:

Sepulveda Camarena D. Computational Chemistry as a Tool for Understanding Non-Covalent Interactions in Organic Reactions and Materials. [Doctoral Dissertation]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/154033

23. Ducos, Paul. Synthèse de nouveaux acides de Lewis silylés pour la catalyse organique : Synthesis of new silylated Lewis acids for organocatalysis.

Degree: Docteur es, Chimie organique, 2015, Bordeaux

A l’inverse des carbocations dont l’existence a pu être prouvée dès le début des années 60, les ions silyliums (R3Si+) ont longtemps été supposés comme… (more)

Subjects/Keywords: Silicium; Silylium; Organocatalyse; Silicon; Silylium; Organocatalysis

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APA (6th Edition):

Ducos, P. (2015). Synthèse de nouveaux acides de Lewis silylés pour la catalyse organique : Synthesis of new silylated Lewis acids for organocatalysis. (Doctoral Dissertation). Bordeaux. Retrieved from http://www.theses.fr/2015BORD0439

Chicago Manual of Style (16th Edition):

Ducos, Paul. “Synthèse de nouveaux acides de Lewis silylés pour la catalyse organique : Synthesis of new silylated Lewis acids for organocatalysis.” 2015. Doctoral Dissertation, Bordeaux. Accessed April 22, 2021. http://www.theses.fr/2015BORD0439.

MLA Handbook (7th Edition):

Ducos, Paul. “Synthèse de nouveaux acides de Lewis silylés pour la catalyse organique : Synthesis of new silylated Lewis acids for organocatalysis.” 2015. Web. 22 Apr 2021.

Vancouver:

Ducos P. Synthèse de nouveaux acides de Lewis silylés pour la catalyse organique : Synthesis of new silylated Lewis acids for organocatalysis. [Internet] [Doctoral dissertation]. Bordeaux; 2015. [cited 2021 Apr 22]. Available from: http://www.theses.fr/2015BORD0439.

Council of Science Editors:

Ducos P. Synthèse de nouveaux acides de Lewis silylés pour la catalyse organique : Synthesis of new silylated Lewis acids for organocatalysis. [Doctoral Dissertation]. Bordeaux; 2015. Available from: http://www.theses.fr/2015BORD0439

24. Bécart, Diane. Bioinspired catalysis using oligourea helical foldamers : Catalyse biomimétique avec des foldamères à strucure hélicoïdale comportant des motifs oligo-(thio)urées.

Degree: Docteur es, Chimie organique, 2017, Bordeaux; Universidad del País Vasco

Catalyse et repliement sont deux notions intimement liées dans la Nature à travers les protéines et les enzymes, puis par extension, avec les catalyseurs synthétiques… (more)

Subjects/Keywords: Foldamères; Oligourea; Organocatalyse; Foldamers; Oligourea; Organocatalysis

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APA (6th Edition):

Bécart, D. (2017). Bioinspired catalysis using oligourea helical foldamers : Catalyse biomimétique avec des foldamères à strucure hélicoïdale comportant des motifs oligo-(thio)urées. (Doctoral Dissertation). Bordeaux; Universidad del País Vasco. Retrieved from http://www.theses.fr/2017BORD0717

Chicago Manual of Style (16th Edition):

Bécart, Diane. “Bioinspired catalysis using oligourea helical foldamers : Catalyse biomimétique avec des foldamères à strucure hélicoïdale comportant des motifs oligo-(thio)urées.” 2017. Doctoral Dissertation, Bordeaux; Universidad del País Vasco. Accessed April 22, 2021. http://www.theses.fr/2017BORD0717.

MLA Handbook (7th Edition):

Bécart, Diane. “Bioinspired catalysis using oligourea helical foldamers : Catalyse biomimétique avec des foldamères à strucure hélicoïdale comportant des motifs oligo-(thio)urées.” 2017. Web. 22 Apr 2021.

Vancouver:

Bécart D. Bioinspired catalysis using oligourea helical foldamers : Catalyse biomimétique avec des foldamères à strucure hélicoïdale comportant des motifs oligo-(thio)urées. [Internet] [Doctoral dissertation]. Bordeaux; Universidad del País Vasco; 2017. [cited 2021 Apr 22]. Available from: http://www.theses.fr/2017BORD0717.

Council of Science Editors:

Bécart D. Bioinspired catalysis using oligourea helical foldamers : Catalyse biomimétique avec des foldamères à strucure hélicoïdale comportant des motifs oligo-(thio)urées. [Doctoral Dissertation]. Bordeaux; Universidad del País Vasco; 2017. Available from: http://www.theses.fr/2017BORD0717

25. Ng, Peter J. Directed Organocatalytic Intermolecular Cope-type Hydroamination of Alkenes .

Degree: 2011, University of Ottawa

 Intermolecular reactions are inherently more difficult than intramolecular reactions, and several transformations can only occur as cyclizations, often to form 5-membered rings. The use of… (more)

Subjects/Keywords: Organocatalysis; Hydroamination

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APA (6th Edition):

Ng, P. J. (2011). Directed Organocatalytic Intermolecular Cope-type Hydroamination of Alkenes . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/19895

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):

Ng, Peter J. “Directed Organocatalytic Intermolecular Cope-type Hydroamination of Alkenes .” 2011. Thesis, University of Ottawa. Accessed April 22, 2021. http://hdl.handle.net/10393/19895.

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

MLA Handbook (7th Edition):

Ng, Peter J. “Directed Organocatalytic Intermolecular Cope-type Hydroamination of Alkenes .” 2011. Web. 22 Apr 2021.

Vancouver:

Ng PJ. Directed Organocatalytic Intermolecular Cope-type Hydroamination of Alkenes . [Internet] [Thesis]. University of Ottawa; 2011. [cited 2021 Apr 22]. Available from: http://hdl.handle.net/10393/19895.

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

Council of Science Editors:

Ng PJ. Directed Organocatalytic Intermolecular Cope-type Hydroamination of Alkenes . [Thesis]. University of Ottawa; 2011. Available from: http://hdl.handle.net/10393/19895

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


University of Houston

26. Jansone-Popova, Santa 1985-. Synthesis of Polycyclic Ring Systems Via C-H Bond Insertion and Enantioselective Conjugate Addition.

Degree: PhD, Chemistry, 2014, University of Houston

 This dissertation presents three main projects. The first discusses synthetic strategies towards the total synthesis of the natural product Maoecrystal V. The second part presents… (more)

Subjects/Keywords: C-H bond insertion; Organic synthesis; Organocatalysis

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APA (6th Edition):

Jansone-Popova, S. 1. (2014). Synthesis of Polycyclic Ring Systems Via C-H Bond Insertion and Enantioselective Conjugate Addition. (Doctoral Dissertation). University of Houston. Retrieved from http://hdl.handle.net/10657/1950

Chicago Manual of Style (16th Edition):

Jansone-Popova, Santa 1985-. “Synthesis of Polycyclic Ring Systems Via C-H Bond Insertion and Enantioselective Conjugate Addition.” 2014. Doctoral Dissertation, University of Houston. Accessed April 22, 2021. http://hdl.handle.net/10657/1950.

MLA Handbook (7th Edition):

Jansone-Popova, Santa 1985-. “Synthesis of Polycyclic Ring Systems Via C-H Bond Insertion and Enantioselective Conjugate Addition.” 2014. Web. 22 Apr 2021.

Vancouver:

Jansone-Popova S1. Synthesis of Polycyclic Ring Systems Via C-H Bond Insertion and Enantioselective Conjugate Addition. [Internet] [Doctoral dissertation]. University of Houston; 2014. [cited 2021 Apr 22]. Available from: http://hdl.handle.net/10657/1950.

Council of Science Editors:

Jansone-Popova S1. Synthesis of Polycyclic Ring Systems Via C-H Bond Insertion and Enantioselective Conjugate Addition. [Doctoral Dissertation]. University of Houston; 2014. Available from: http://hdl.handle.net/10657/1950

27. Flanigan, Darrin Miles. Development of asymmetric N-heterocyclic carbene-catalyzed reactions.

Degree: PhD, Chemistry, 2017, Colorado State University

 N-Heterocyclic carbenes (NHCs) are ubiquitous organocatalysts in a variety of asymmetric transformations. The benzoin and Stetter reactions, which couple aldehydes to other aldehydes or Michael… (more)

Subjects/Keywords: organic chemistry; n-heterocyclic carbenes; organocatalysis

Page 1 Page 2 Page 3 Page 4 Page 5 Page 6 Page 7 Sample image

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APA (6th Edition):

Flanigan, D. M. (2017). Development of asymmetric N-heterocyclic carbene-catalyzed reactions. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/183966

Chicago Manual of Style (16th Edition):

Flanigan, Darrin Miles. “Development of asymmetric N-heterocyclic carbene-catalyzed reactions.” 2017. Doctoral Dissertation, Colorado State University. Accessed April 22, 2021. http://hdl.handle.net/10217/183966.

MLA Handbook (7th Edition):

Flanigan, Darrin Miles. “Development of asymmetric N-heterocyclic carbene-catalyzed reactions.” 2017. Web. 22 Apr 2021.

Vancouver:

Flanigan DM. Development of asymmetric N-heterocyclic carbene-catalyzed reactions. [Internet] [Doctoral dissertation]. Colorado State University; 2017. [cited 2021 Apr 22]. Available from: http://hdl.handle.net/10217/183966.

Council of Science Editors:

Flanigan DM. Development of asymmetric N-heterocyclic carbene-catalyzed reactions. [Doctoral Dissertation]. Colorado State University; 2017. Available from: http://hdl.handle.net/10217/183966


Colorado State University

28. 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 April 22, 2021. 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. 22 Apr 2021.

Vancouver:

Glover GS. Development of an asymmetric intermolecular stetter reaction and organocatalyst design. [Internet] [Masters thesis]. Colorado State University; 2012. [cited 2021 Apr 22]. 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


Universitat Rovira i Virgili

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

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 April 22, 2021. 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. 22 Apr 2021.

Vancouver:

Alza Barrios E. Approaches to asymmetric catalysis with polymer-supported pyrrolidines. [Internet] [Thesis]. Universitat Rovira i Virgili; 2011. [cited 2021 Apr 22]. 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 Manitoba

30. Singh, Simarpreet. Computational investigations of reactivity and selectivity in addition reactions.

Degree: Chemistry, 2018, University of Manitoba

 The development and application of density functional theory (DFT) on real chemical systems has allowed experimentalists to use computational chemistry, without an understanding of mathematical… (more)

Subjects/Keywords: Density Functional Theory; Organocatalysis; Asymmetric Synthesis

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

APA (6th Edition):

Singh, S. (2018). Computational investigations of reactivity and selectivity in addition reactions. (Masters Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/33677

Chicago Manual of Style (16th Edition):

Singh, Simarpreet. “Computational investigations of reactivity and selectivity in addition reactions.” 2018. Masters Thesis, University of Manitoba. Accessed April 22, 2021. http://hdl.handle.net/1993/33677.

MLA Handbook (7th Edition):

Singh, Simarpreet. “Computational investigations of reactivity and selectivity in addition reactions.” 2018. Web. 22 Apr 2021.

Vancouver:

Singh S. Computational investigations of reactivity and selectivity in addition reactions. [Internet] [Masters thesis]. University of Manitoba; 2018. [cited 2021 Apr 22]. Available from: http://hdl.handle.net/1993/33677.

Council of Science Editors:

Singh S. Computational investigations of reactivity and selectivity in addition reactions. [Masters Thesis]. University of Manitoba; 2018. Available from: http://hdl.handle.net/1993/33677

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