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You searched for subject:(organocatalysis). Showing records 1 – 30 of 295 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 August 14, 2020. 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. 14 Aug 2020.

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 2020 Aug 14]. 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 August 14, 2020. 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. 14 Aug 2020.

Vancouver:

Farley AJM. Development and application of a new class of potent bifunctional organocatalysts. [Internet] [Doctoral dissertation]. University of Oxford; 2015. [cited 2020 Aug 14]. 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 August 14, 2020. 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. 14 Aug 2020.

Vancouver:

Taylor JE. New applications of organocatalysis. [Internet] [Doctoral dissertation]. University of Bath; 2011. [cited 2020 Aug 14]. 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 August 14, 2020. 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. 14 Aug 2020.

Vancouver:

Johnston RC. Rationalization and innovative design of asymmetric organocatalysts through computational investigation. [Internet] [Doctoral dissertation]. Oregon State University; 2015. [cited 2020 Aug 14]. 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


Texas A&M University

5. 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 August 14, 2020. 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. 14 Aug 2020.

Vancouver:

Abbasov ME. Diels–Alder–Initiated Organocascades Employing Acylammonium Catalysis: Scope, Mechanism, and Application. [Internet] [Doctoral dissertation]. Texas A&M University; 2015. [cited 2020 Aug 14]. 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

6. 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 August 14, 2020. http://hdl.handle.net/1969.1/153374.

MLA Handbook (7th Edition):

Khamatnurova, Tatyana. “Phase Selectively Soluble Polystyrene-Supported Organocatalysts.” 2014. Web. 14 Aug 2020.

Vancouver:

Khamatnurova T. Phase Selectively Soluble Polystyrene-Supported Organocatalysts. [Internet] [Doctoral dissertation]. Texas A&M University; 2014. [cited 2020 Aug 14]. 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

7. 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 August 14, 2020. 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. 14 Aug 2020.

Vancouver:

Nielsen AJ. Novel Wittig and Organocatalytic Methodologies for the Synthesis of Chemotherapeutic Compounds. [Internet] [Doctoral dissertation]. McMaster University; 2019. [cited 2020 Aug 14]. 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

8. 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 August 14, 2020. 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. 14 Aug 2020.

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 2020 Aug 14]. 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 Michigan

9. 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 August 14, 2020. 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. 14 Aug 2020.

Vancouver:

Winschel GA. Chiral Phosphoric Acid-Catalyzed Stereoselective Transformations of Vinyl Ethers and Acetals. [Internet] [Doctoral dissertation]. University of Michigan; 2015. [cited 2020 Aug 14]. 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

10. 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 August 14, 2020. 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. 14 Aug 2020.

Vancouver:

CRONIN S. Practical and enantioselective amino acid synthesis via novel catalytic ring opening processes. [Internet] [Thesis]. Trinity College Dublin; 2019. [cited 2020 Aug 14]. 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 Houston

11. 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 August 14, 2020. http://hdl.handle.net/10657/6552.

MLA Handbook (7th Edition):

Vallakati, Ravikrishna 1977-. “Synthesis of the Antimalarial Flindersial Alkaloids.” 2015. Web. 14 Aug 2020.

Vancouver:

Vallakati R1. Synthesis of the Antimalarial Flindersial Alkaloids. [Internet] [Doctoral dissertation]. University of Houston; 2015. [cited 2020 Aug 14]. 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


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 August 14, 2020. http://hdl.handle.net/2142/95493.

MLA Handbook (7th Edition):

Kornfilt, David Jean Pierre. “Lewis base catalyzed enantioselective oxysulfenylation of alkenes.” 2016. Web. 14 Aug 2020.

Vancouver:

Kornfilt DJP. Lewis base catalyzed enantioselective oxysulfenylation of alkenes. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2020 Aug 14]. 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 August 14, 2020. https://digitalrepository.unm.edu/chem_etds/27.

MLA Handbook (7th Edition):

Zhang, Xinshuai. “Alkynal involved organocatalytic reactions.” 2012. Web. 14 Aug 2020.

Vancouver:

Zhang X. Alkynal involved organocatalytic reactions. [Internet] [Doctoral dissertation]. University of New Mexico; 2012. [cited 2020 Aug 14]. 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 August 14, 2020. http://hdl.handle.net/1853/60207.

MLA Handbook (7th Edition):

Bakr, Brandon Wallace. “Symmetry-adapted perturbation theory for organocatalysis.” 2018. Web. 14 Aug 2020.

Vancouver:

Bakr BW. Symmetry-adapted perturbation theory for organocatalysis. [Internet] [Doctoral dissertation]. Georgia Tech; 2018. [cited 2020 Aug 14]. 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 August 14, 2020. 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. 14 Aug 2020.

Vancouver:

Haugeberg BJ. Development and Application of Quinone-Catalyzed C-C Bond Cleavage. [Internet] [Masters thesis]. University of Kansas; 2016. [cited 2020 Aug 14]. 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 California – Berkeley

16. 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 August 14, 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. 14 Aug 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 Aug 14]. 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


Texas A&M University

17. 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 August 14, 2020. 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. 14 Aug 2020.

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 2020 Aug 14]. 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


University of Pennsylvania

18. Walvoord, Ryan R. Part I: Nitroalkane Transformations: Synthesis of Vicinal Diamines and Arylnitromethanes Part II: Quantification of Electrophile Lumo-Lowering via Colorimetric Probes.

Degree: 2014, University of Pennsylvania

 Part I of this dissertation focuses on the synthetic chemistry of arylnitromethanes as both products and reactants. Use of these compounds as key building blocks… (more)

Subjects/Keywords: Hydrogen Bonding; Organocatalysis; Palladium Catalysis; Organic Chemistry

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APA (6th Edition):

Walvoord, R. R. (2014). Part I: Nitroalkane Transformations: Synthesis of Vicinal Diamines and Arylnitromethanes Part II: Quantification of Electrophile Lumo-Lowering via Colorimetric Probes. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/1490

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):

Walvoord, Ryan R. “Part I: Nitroalkane Transformations: Synthesis of Vicinal Diamines and Arylnitromethanes Part II: Quantification of Electrophile Lumo-Lowering via Colorimetric Probes.” 2014. Thesis, University of Pennsylvania. Accessed August 14, 2020. https://repository.upenn.edu/edissertations/1490.

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

MLA Handbook (7th Edition):

Walvoord, Ryan R. “Part I: Nitroalkane Transformations: Synthesis of Vicinal Diamines and Arylnitromethanes Part II: Quantification of Electrophile Lumo-Lowering via Colorimetric Probes.” 2014. Web. 14 Aug 2020.

Vancouver:

Walvoord RR. Part I: Nitroalkane Transformations: Synthesis of Vicinal Diamines and Arylnitromethanes Part II: Quantification of Electrophile Lumo-Lowering via Colorimetric Probes. [Internet] [Thesis]. University of Pennsylvania; 2014. [cited 2020 Aug 14]. Available from: https://repository.upenn.edu/edissertations/1490.

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

Council of Science Editors:

Walvoord RR. Part I: Nitroalkane Transformations: Synthesis of Vicinal Diamines and Arylnitromethanes Part II: Quantification of Electrophile Lumo-Lowering via Colorimetric Probes. [Thesis]. University of Pennsylvania; 2014. Available from: https://repository.upenn.edu/edissertations/1490

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 August 14, 2020. 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. 14 Aug 2020.

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 2020 Aug 14]. 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

20. 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 August 14, 2020. 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. 14 Aug 2020.

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 2020 Aug 14]. 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

21. 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 August 14, 2020. 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. 14 Aug 2020.

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 2020 Aug 14]. 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


Vanderbilt University

22. 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://etd.library.vanderbilt.edu/available/etd-12082015-110505/ ;

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 August 14, 2020. http://etd.library.vanderbilt.edu/available/etd-12082015-110505/ ;.

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. 14 Aug 2020.

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 2020 Aug 14]. Available from: http://etd.library.vanderbilt.edu/available/etd-12082015-110505/ ;.

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://etd.library.vanderbilt.edu/available/etd-12082015-110505/ ;

23. 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 August 14, 2020. 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. 14 Aug 2020.

Vancouver:

Ng PJ. Directed Organocatalytic Intermolecular Cope-type Hydroamination of Alkenes . [Internet] [Thesis]. University of Ottawa; 2011. [cited 2020 Aug 14]. 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


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 August 14, 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. 14 Aug 2020.

Vancouver:

Alza Barrios E. Approaches to asymmetric catalysis with polymer-supported pyrrolidines. [Internet] [Thesis]. Universitat Rovira i Virgili; 2011. [cited 2020 Aug 14]. 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


Cornell University

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

Degree: 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 . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/31490

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):

Opalka, Suzanne. “Development Of Catalytic Systems In Batch And Flow Using Dual Organocatalysts And Solid Packed-Bed Reactors .” 2012. Thesis, Cornell University. Accessed August 14, 2020. http://hdl.handle.net/1813/31490.

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

MLA Handbook (7th Edition):

Opalka, Suzanne. “Development Of Catalytic Systems In Batch And Flow Using Dual Organocatalysts And Solid Packed-Bed Reactors .” 2012. Web. 14 Aug 2020.

Vancouver:

Opalka S. Development Of Catalytic Systems In Batch And Flow Using Dual Organocatalysts And Solid Packed-Bed Reactors . [Internet] [Thesis]. Cornell University; 2012. [cited 2020 Aug 14]. Available from: http://hdl.handle.net/1813/31490.

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

Council of Science Editors:

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

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


University of New South Wales

26. Barnett, Christopher. Investigating N-heterocyclic carbene electronic characteristics.

Degree: Chemistry, 2019, University of New South Wales

 Three main subsets of the imidazol-2-ylidene scaffold have been synthesised and their electronic properties have been investigated. The respective [PdBr2(iPrBenz)(L)] complexes, where L = the… (more)

Subjects/Keywords: Palladium; NHC; Selenone; Imidazolium; Halogen; Electronic; Organocatalysis

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APA (6th Edition):

Barnett, C. (2019). Investigating N-heterocyclic carbene electronic characteristics. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/62204

Chicago Manual of Style (16th Edition):

Barnett, Christopher. “Investigating N-heterocyclic carbene electronic characteristics.” 2019. Doctoral Dissertation, University of New South Wales. Accessed August 14, 2020. http://handle.unsw.edu.au/1959.4/62204.

MLA Handbook (7th Edition):

Barnett, Christopher. “Investigating N-heterocyclic carbene electronic characteristics.” 2019. Web. 14 Aug 2020.

Vancouver:

Barnett C. Investigating N-heterocyclic carbene electronic characteristics. [Internet] [Doctoral dissertation]. University of New South Wales; 2019. [cited 2020 Aug 14]. Available from: http://handle.unsw.edu.au/1959.4/62204.

Council of Science Editors:

Barnett C. Investigating N-heterocyclic carbene electronic characteristics. [Doctoral Dissertation]. University of New South Wales; 2019. Available from: http://handle.unsw.edu.au/1959.4/62204


University of St Andrews

27. Douglas, James J. NHCs in organocatalysis : azolium enolate generation and synthetic applications.

Degree: PhD, 2012, University of St Andrews

 This thesis details investigations into organocatalytic reactions promoted by N Heterocyclic Carbenes (NHCs) that proceed via an assumed azolium enolate intermediate. Initial research focused on… (more)

Subjects/Keywords: 631.4; Catalysis; Organocatalysis; N-Heterocyclic carbenes; Ketenes

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APA (6th Edition):

Douglas, J. J. (2012). NHCs in organocatalysis : azolium enolate generation and synthetic applications. (Doctoral Dissertation). University of St Andrews. Retrieved from http://hdl.handle.net/10023/3085

Chicago Manual of Style (16th Edition):

Douglas, James J. “NHCs in organocatalysis : azolium enolate generation and synthetic applications.” 2012. Doctoral Dissertation, University of St Andrews. Accessed August 14, 2020. http://hdl.handle.net/10023/3085.

MLA Handbook (7th Edition):

Douglas, James J. “NHCs in organocatalysis : azolium enolate generation and synthetic applications.” 2012. Web. 14 Aug 2020.

Vancouver:

Douglas JJ. NHCs in organocatalysis : azolium enolate generation and synthetic applications. [Internet] [Doctoral dissertation]. University of St Andrews; 2012. [cited 2020 Aug 14]. Available from: http://hdl.handle.net/10023/3085.

Council of Science Editors:

Douglas JJ. NHCs in organocatalysis : azolium enolate generation and synthetic applications. [Doctoral Dissertation]. University of St Andrews; 2012. Available from: http://hdl.handle.net/10023/3085


Princeton University

28. Welin, Eric Robert. New Concepts in Catalysis: The Development of Photoredox Catalysis as a Powerful Synthetic Tool .

Degree: PhD, 2015, Princeton University

 In the last half-century few developments have changed the chemical community more than the development of novel forms of catalysis. As a result of the… (more)

Subjects/Keywords: Catalysis; Enantioselective; Organic Chemistry; Organocatalysis; Photoredox; Synthesis

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

APA (6th Edition):

Welin, E. R. (2015). New Concepts in Catalysis: The Development of Photoredox Catalysis as a Powerful Synthetic Tool . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp011831cn340

Chicago Manual of Style (16th Edition):

Welin, Eric Robert. “New Concepts in Catalysis: The Development of Photoredox Catalysis as a Powerful Synthetic Tool .” 2015. Doctoral Dissertation, Princeton University. Accessed August 14, 2020. http://arks.princeton.edu/ark:/88435/dsp011831cn340.

MLA Handbook (7th Edition):

Welin, Eric Robert. “New Concepts in Catalysis: The Development of Photoredox Catalysis as a Powerful Synthetic Tool .” 2015. Web. 14 Aug 2020.

Vancouver:

Welin ER. New Concepts in Catalysis: The Development of Photoredox Catalysis as a Powerful Synthetic Tool . [Internet] [Doctoral dissertation]. Princeton University; 2015. [cited 2020 Aug 14]. Available from: http://arks.princeton.edu/ark:/88435/dsp011831cn340.

Council of Science Editors:

Welin ER. New Concepts in Catalysis: The Development of Photoredox Catalysis as a Powerful Synthetic Tool . [Doctoral Dissertation]. Princeton University; 2015. Available from: http://arks.princeton.edu/ark:/88435/dsp011831cn340


Princeton University

29. Liu, Chun. New Frontiers in Organocatalysis and Photoredox Catalysis .

Degree: PhD, 2017, Princeton University

 Despite the development of numerous modern synthetic methodologies that have enabled the building of useful bond connections, there remains a need for ever more powerful… (more)

Subjects/Keywords: bioconjugation; organocatalysis; oxy-allyl cation; photoredox catalysis

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

APA (6th Edition):

Liu, C. (2017). New Frontiers in Organocatalysis and Photoredox Catalysis . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp018c97kt029

Chicago Manual of Style (16th Edition):

Liu, Chun. “New Frontiers in Organocatalysis and Photoredox Catalysis .” 2017. Doctoral Dissertation, Princeton University. Accessed August 14, 2020. http://arks.princeton.edu/ark:/88435/dsp018c97kt029.

MLA Handbook (7th Edition):

Liu, Chun. “New Frontiers in Organocatalysis and Photoredox Catalysis .” 2017. Web. 14 Aug 2020.

Vancouver:

Liu C. New Frontiers in Organocatalysis and Photoredox Catalysis . [Internet] [Doctoral dissertation]. Princeton University; 2017. [cited 2020 Aug 14]. Available from: http://arks.princeton.edu/ark:/88435/dsp018c97kt029.

Council of Science Editors:

Liu C. New Frontiers in Organocatalysis and Photoredox Catalysis . [Doctoral Dissertation]. Princeton University; 2017. Available from: http://arks.princeton.edu/ark:/88435/dsp018c97kt029

30. Sasso d'Elia, Cecilia. Organocatalyse et multiple bond-forming transformations (MBFTs) comme outils pour le contrôle de la chiralité : Organocatalysis and multiple bond-forming transformations as tools to control chirality.

Degree: Docteur es, Chimie organique, 2017, Aix Marseille Université

Depuis des dizaines d’années, les chimistes organiciens ont accru leurs capacités à synthétiser des molécules complexes de manière exponentielle par le développement de nouvelles méthodes… (more)

Subjects/Keywords: Organocatalyse; Chiralitè; MBFTs; Organocatalysis; Chirality; MBFTs

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

APA (6th Edition):

Sasso d'Elia, C. (2017). Organocatalyse et multiple bond-forming transformations (MBFTs) comme outils pour le contrôle de la chiralité : Organocatalysis and multiple bond-forming transformations as tools to control chirality. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2017AIXM0371

Chicago Manual of Style (16th Edition):

Sasso d'Elia, Cecilia. “Organocatalyse et multiple bond-forming transformations (MBFTs) comme outils pour le contrôle de la chiralité : Organocatalysis and multiple bond-forming transformations as tools to control chirality.” 2017. Doctoral Dissertation, Aix Marseille Université. Accessed August 14, 2020. http://www.theses.fr/2017AIXM0371.

MLA Handbook (7th Edition):

Sasso d'Elia, Cecilia. “Organocatalyse et multiple bond-forming transformations (MBFTs) comme outils pour le contrôle de la chiralité : Organocatalysis and multiple bond-forming transformations as tools to control chirality.” 2017. Web. 14 Aug 2020.

Vancouver:

Sasso d'Elia C. Organocatalyse et multiple bond-forming transformations (MBFTs) comme outils pour le contrôle de la chiralité : Organocatalysis and multiple bond-forming transformations as tools to control chirality. [Internet] [Doctoral dissertation]. Aix Marseille Université 2017. [cited 2020 Aug 14]. Available from: http://www.theses.fr/2017AIXM0371.

Council of Science Editors:

Sasso d'Elia C. Organocatalyse et multiple bond-forming transformations (MBFTs) comme outils pour le contrôle de la chiralité : Organocatalysis and multiple bond-forming transformations as tools to control chirality. [Doctoral Dissertation]. Aix Marseille Université 2017. Available from: http://www.theses.fr/2017AIXM0371

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