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You searched for +publisher:"University of South Carolina" +contributor:("Sheryl L Wiskur"). Showing records 1 – 8 of 8 total matches.

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University of South Carolina

1. Clark, Robert W. A Silylation-Based Kinetic Resolution of Hydroxy Lactones and Lactams with Subsequent Mechanistic Investigations.

Degree: PhD, Chemistry and Biochemistry, 2015, University of South Carolina

  The work contained herein focuses on the methodology and design of new reactions for the production of stereoenriched compounds. The primary focus of research… (more)

Subjects/Keywords: Chemistry; Physical Sciences and Mathematics; Silylation-Based Kinetic Resolution; Hydroxy Lactones; Lactams; Subsequent Mechanistic Investigations

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APA (6th Edition):

Clark, R. W. (2015). A Silylation-Based Kinetic Resolution of Hydroxy Lactones and Lactams with Subsequent Mechanistic Investigations. (Doctoral Dissertation). University of South Carolina. Retrieved from https://scholarcommons.sc.edu/etd/3662

Chicago Manual of Style (16th Edition):

Clark, Robert W. “A Silylation-Based Kinetic Resolution of Hydroxy Lactones and Lactams with Subsequent Mechanistic Investigations.” 2015. Doctoral Dissertation, University of South Carolina. Accessed June 17, 2019. https://scholarcommons.sc.edu/etd/3662.

MLA Handbook (7th Edition):

Clark, Robert W. “A Silylation-Based Kinetic Resolution of Hydroxy Lactones and Lactams with Subsequent Mechanistic Investigations.” 2015. Web. 17 Jun 2019.

Vancouver:

Clark RW. A Silylation-Based Kinetic Resolution of Hydroxy Lactones and Lactams with Subsequent Mechanistic Investigations. [Internet] [Doctoral dissertation]. University of South Carolina; 2015. [cited 2019 Jun 17]. Available from: https://scholarcommons.sc.edu/etd/3662.

Council of Science Editors:

Clark RW. A Silylation-Based Kinetic Resolution of Hydroxy Lactones and Lactams with Subsequent Mechanistic Investigations. [Doctoral Dissertation]. University of South Carolina; 2015. Available from: https://scholarcommons.sc.edu/etd/3662


University of South Carolina

2. Patel, Sachin Girish. The Kinetic Resolution of Secondary Alcohols Through A Tandem Enantioselective Silylation and the Synthesis of Bis(Oxazolidinyl)Pyridine Metal-Organic Complexes.

Degree: PhD, Chemistry and Biochemistry, 2010, University of South Carolina

  This dissertation details our efforts to design and implement mild conditions in which to carry out the Mukaiyama aldol reaction. The design of a… (more)

Subjects/Keywords: Chemistry; Physical Sciences and Mathematics; Organic Chemistry; Kinetic Resolution; Enantioselective Silylation; Metal-Organic Complexes

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APA (6th Edition):

Patel, S. G. (2010). The Kinetic Resolution of Secondary Alcohols Through A Tandem Enantioselective Silylation and the Synthesis of Bis(Oxazolidinyl)Pyridine Metal-Organic Complexes. (Doctoral Dissertation). University of South Carolina. Retrieved from https://scholarcommons.sc.edu/etd/716

Chicago Manual of Style (16th Edition):

Patel, Sachin Girish. “The Kinetic Resolution of Secondary Alcohols Through A Tandem Enantioselective Silylation and the Synthesis of Bis(Oxazolidinyl)Pyridine Metal-Organic Complexes.” 2010. Doctoral Dissertation, University of South Carolina. Accessed June 17, 2019. https://scholarcommons.sc.edu/etd/716.

MLA Handbook (7th Edition):

Patel, Sachin Girish. “The Kinetic Resolution of Secondary Alcohols Through A Tandem Enantioselective Silylation and the Synthesis of Bis(Oxazolidinyl)Pyridine Metal-Organic Complexes.” 2010. Web. 17 Jun 2019.

Vancouver:

Patel SG. The Kinetic Resolution of Secondary Alcohols Through A Tandem Enantioselective Silylation and the Synthesis of Bis(Oxazolidinyl)Pyridine Metal-Organic Complexes. [Internet] [Doctoral dissertation]. University of South Carolina; 2010. [cited 2019 Jun 17]. Available from: https://scholarcommons.sc.edu/etd/716.

Council of Science Editors:

Patel SG. The Kinetic Resolution of Secondary Alcohols Through A Tandem Enantioselective Silylation and the Synthesis of Bis(Oxazolidinyl)Pyridine Metal-Organic Complexes. [Doctoral Dissertation]. University of South Carolina; 2010. Available from: https://scholarcommons.sc.edu/etd/716


University of South Carolina

3. Sheppard, Cody Ian. A Silylation Based Kinetic Resolution of Secondary Alcohols And The Synthesis And Structural Characterization of Pyridyl-oxazolidine Compounds.

Degree: PhD, Chemistry and Biochemistry, 2013, University of South Carolina

  Described herein is the first enantioselective silylation based kinetic resolution of monofunctional secondary alcohols to achieve useful levels of enantioselectivity. Using commercially available reagents,… (more)

Subjects/Keywords: Chemistry; Physical Sciences and Mathematics; 29Silicon-NMR; Chemical sensing; Circular Dichroism; Kinetic Resolution; Organocatalysis; Silylation

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APA (6th Edition):

Sheppard, C. I. (2013). A Silylation Based Kinetic Resolution of Secondary Alcohols And The Synthesis And Structural Characterization of Pyridyl-oxazolidine Compounds. (Doctoral Dissertation). University of South Carolina. Retrieved from https://scholarcommons.sc.edu/etd/734

Chicago Manual of Style (16th Edition):

Sheppard, Cody Ian. “A Silylation Based Kinetic Resolution of Secondary Alcohols And The Synthesis And Structural Characterization of Pyridyl-oxazolidine Compounds.” 2013. Doctoral Dissertation, University of South Carolina. Accessed June 17, 2019. https://scholarcommons.sc.edu/etd/734.

MLA Handbook (7th Edition):

Sheppard, Cody Ian. “A Silylation Based Kinetic Resolution of Secondary Alcohols And The Synthesis And Structural Characterization of Pyridyl-oxazolidine Compounds.” 2013. Web. 17 Jun 2019.

Vancouver:

Sheppard CI. A Silylation Based Kinetic Resolution of Secondary Alcohols And The Synthesis And Structural Characterization of Pyridyl-oxazolidine Compounds. [Internet] [Doctoral dissertation]. University of South Carolina; 2013. [cited 2019 Jun 17]. Available from: https://scholarcommons.sc.edu/etd/734.

Council of Science Editors:

Sheppard CI. A Silylation Based Kinetic Resolution of Secondary Alcohols And The Synthesis And Structural Characterization of Pyridyl-oxazolidine Compounds. [Doctoral Dissertation]. University of South Carolina; 2013. Available from: https://scholarcommons.sc.edu/etd/734


University of South Carolina

4. Moore, Maggie Iris. Producing Enantiopure Secondary Alcohols via a Silylation based Kinetic Resolution and a One-Pot Polishing Sequence.

Degree: PhD, Chemistry and Biochemistry, 2012, University of South Carolina

  This dissertation describes our efforts to develop new methods of producing enantiopure compounds through a sequential one-pot polishing procedure and through kinetic resolutions via… (more)

Subjects/Keywords: Chemistry; Physical Sciences and Mathematics; chirality; desilylation; kinetic resolutions; lactone; one-pot; silylation

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APA (6th Edition):

Moore, M. I. (2012). Producing Enantiopure Secondary Alcohols via a Silylation based Kinetic Resolution and a One-Pot Polishing Sequence. (Doctoral Dissertation). University of South Carolina. Retrieved from https://scholarcommons.sc.edu/etd/710

Chicago Manual of Style (16th Edition):

Moore, Maggie Iris. “Producing Enantiopure Secondary Alcohols via a Silylation based Kinetic Resolution and a One-Pot Polishing Sequence.” 2012. Doctoral Dissertation, University of South Carolina. Accessed June 17, 2019. https://scholarcommons.sc.edu/etd/710.

MLA Handbook (7th Edition):

Moore, Maggie Iris. “Producing Enantiopure Secondary Alcohols via a Silylation based Kinetic Resolution and a One-Pot Polishing Sequence.” 2012. Web. 17 Jun 2019.

Vancouver:

Moore MI. Producing Enantiopure Secondary Alcohols via a Silylation based Kinetic Resolution and a One-Pot Polishing Sequence. [Internet] [Doctoral dissertation]. University of South Carolina; 2012. [cited 2019 Jun 17]. Available from: https://scholarcommons.sc.edu/etd/710.

Council of Science Editors:

Moore MI. Producing Enantiopure Secondary Alcohols via a Silylation based Kinetic Resolution and a One-Pot Polishing Sequence. [Doctoral Dissertation]. University of South Carolina; 2012. Available from: https://scholarcommons.sc.edu/etd/710


University of South Carolina

5. Nguyen, Thi-Ngoc Dieu. Asymmetric Allylation of Aldehydes Catalyzed by Formamide Organocatalysts. Studies Towards The Synthesis of L- Domoic Acid Side Chain.

Degree: PhD, Chemistry and Biochemistry, 2010, University of South Carolina

  Part 1 Homoallylic alcohols are versatile synthons in natural product synthesis. They are most efficiently generated by allylation of aldehydes. Classically metal-based Lewis acids… (more)

Subjects/Keywords: Chemistry

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APA (6th Edition):

Nguyen, T. D. (2010). Asymmetric Allylation of Aldehydes Catalyzed by Formamide Organocatalysts. Studies Towards The Synthesis of L- Domoic Acid Side Chain. (Doctoral Dissertation). University of South Carolina. Retrieved from https://scholarcommons.sc.edu/etd/228

Chicago Manual of Style (16th Edition):

Nguyen, Thi-Ngoc Dieu. “Asymmetric Allylation of Aldehydes Catalyzed by Formamide Organocatalysts. Studies Towards The Synthesis of L- Domoic Acid Side Chain.” 2010. Doctoral Dissertation, University of South Carolina. Accessed June 17, 2019. https://scholarcommons.sc.edu/etd/228.

MLA Handbook (7th Edition):

Nguyen, Thi-Ngoc Dieu. “Asymmetric Allylation of Aldehydes Catalyzed by Formamide Organocatalysts. Studies Towards The Synthesis of L- Domoic Acid Side Chain.” 2010. Web. 17 Jun 2019.

Vancouver:

Nguyen TD. Asymmetric Allylation of Aldehydes Catalyzed by Formamide Organocatalysts. Studies Towards The Synthesis of L- Domoic Acid Side Chain. [Internet] [Doctoral dissertation]. University of South Carolina; 2010. [cited 2019 Jun 17]. Available from: https://scholarcommons.sc.edu/etd/228.

Council of Science Editors:

Nguyen TD. Asymmetric Allylation of Aldehydes Catalyzed by Formamide Organocatalysts. Studies Towards The Synthesis of L- Domoic Acid Side Chain. [Doctoral Dissertation]. University of South Carolina; 2010. Available from: https://scholarcommons.sc.edu/etd/228


University of South Carolina

6. Zhang, Yan. Silylation-Based Kinetic Resolution of Α-Hydroxy Carbonyl Compounds and Synthesis of Chiral Isothiourea Catalysts.

Degree: PhD, Chemistry and Biochemistry, 2013, University of South Carolina

  The thesis describes the silylation-based kinetic resolution for α-hydroxy carbonyl compounds catalyzed by isothiourea catalyst as well as our effort to make novel chiral… (more)

Subjects/Keywords: Chemistry; Organic Chemistry; kinetic resolution; silylation; synthesis

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APA (6th Edition):

Zhang, Y. (2013). Silylation-Based Kinetic Resolution of Α-Hydroxy Carbonyl Compounds and Synthesis of Chiral Isothiourea Catalysts. (Doctoral Dissertation). University of South Carolina. Retrieved from https://scholarcommons.sc.edu/etd/2428

Chicago Manual of Style (16th Edition):

Zhang, Yan. “Silylation-Based Kinetic Resolution of Α-Hydroxy Carbonyl Compounds and Synthesis of Chiral Isothiourea Catalysts.” 2013. Doctoral Dissertation, University of South Carolina. Accessed June 17, 2019. https://scholarcommons.sc.edu/etd/2428.

MLA Handbook (7th Edition):

Zhang, Yan. “Silylation-Based Kinetic Resolution of Α-Hydroxy Carbonyl Compounds and Synthesis of Chiral Isothiourea Catalysts.” 2013. Web. 17 Jun 2019.

Vancouver:

Zhang Y. Silylation-Based Kinetic Resolution of Α-Hydroxy Carbonyl Compounds and Synthesis of Chiral Isothiourea Catalysts. [Internet] [Doctoral dissertation]. University of South Carolina; 2013. [cited 2019 Jun 17]. Available from: https://scholarcommons.sc.edu/etd/2428.

Council of Science Editors:

Zhang Y. Silylation-Based Kinetic Resolution of Α-Hydroxy Carbonyl Compounds and Synthesis of Chiral Isothiourea Catalysts. [Doctoral Dissertation]. University of South Carolina; 2013. Available from: https://scholarcommons.sc.edu/etd/2428


University of South Carolina

7. Wang, Li. Silylation-Based Kinetic Resolution of 2-Arylcyclohexanols and Understanding Internal Chirality Transmission via Circular Dichroism.

Degree: PhD, Chemistry and Biochemistry, 2017, University of South Carolina

  This work described herein focuses on the silylation-based kinetic resolution methodology developed by the Wiskur group in 2011. It is a powerful method for… (more)

Subjects/Keywords: Chemistry; Physical Sciences and Mathematics; 2-Arylcyclohexanols; Circular Dichroism

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APA (6th Edition):

Wang, L. (2017). Silylation-Based Kinetic Resolution of 2-Arylcyclohexanols and Understanding Internal Chirality Transmission via Circular Dichroism. (Doctoral Dissertation). University of South Carolina. Retrieved from https://scholarcommons.sc.edu/etd/4246

Chicago Manual of Style (16th Edition):

Wang, Li. “Silylation-Based Kinetic Resolution of 2-Arylcyclohexanols and Understanding Internal Chirality Transmission via Circular Dichroism.” 2017. Doctoral Dissertation, University of South Carolina. Accessed June 17, 2019. https://scholarcommons.sc.edu/etd/4246.

MLA Handbook (7th Edition):

Wang, Li. “Silylation-Based Kinetic Resolution of 2-Arylcyclohexanols and Understanding Internal Chirality Transmission via Circular Dichroism.” 2017. Web. 17 Jun 2019.

Vancouver:

Wang L. Silylation-Based Kinetic Resolution of 2-Arylcyclohexanols and Understanding Internal Chirality Transmission via Circular Dichroism. [Internet] [Doctoral dissertation]. University of South Carolina; 2017. [cited 2019 Jun 17]. Available from: https://scholarcommons.sc.edu/etd/4246.

Council of Science Editors:

Wang L. Silylation-Based Kinetic Resolution of 2-Arylcyclohexanols and Understanding Internal Chirality Transmission via Circular Dichroism. [Doctoral Dissertation]. University of South Carolina; 2017. Available from: https://scholarcommons.sc.edu/etd/4246

8. AKHANI, RAVISH K. Mechanistic Investigation of a Silylation-Based Kinetic Resolution Using Linear Free Energy Relationships and Its Application to Substrate Expansion and Polymer Supported Kinetic Resolutions.

Degree: PhD, Chemistry and Biochemistry, 2014, University of South Carolina

  This dissertation represents our preliminary mechanistic investigations on the silylation-based kinetic resolution of secondary alcohols, and how we use that knowledge for further expansion… (more)

Subjects/Keywords: Chemistry; Physical Sciences and Mathematics; Kinetic Resolution; Linear Free Energy Relationships; Mechanism; Selectivity factor; Silylation

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APA (6th Edition):

AKHANI, R. K. (2014). Mechanistic Investigation of a Silylation-Based Kinetic Resolution Using Linear Free Energy Relationships and Its Application to Substrate Expansion and Polymer Supported Kinetic Resolutions. (Doctoral Dissertation). University of South Carolina. Retrieved from https://scholarcommons.sc.edu/etd/2785

Chicago Manual of Style (16th Edition):

AKHANI, RAVISH K. “Mechanistic Investigation of a Silylation-Based Kinetic Resolution Using Linear Free Energy Relationships and Its Application to Substrate Expansion and Polymer Supported Kinetic Resolutions.” 2014. Doctoral Dissertation, University of South Carolina. Accessed June 17, 2019. https://scholarcommons.sc.edu/etd/2785.

MLA Handbook (7th Edition):

AKHANI, RAVISH K. “Mechanistic Investigation of a Silylation-Based Kinetic Resolution Using Linear Free Energy Relationships and Its Application to Substrate Expansion and Polymer Supported Kinetic Resolutions.” 2014. Web. 17 Jun 2019.

Vancouver:

AKHANI RK. Mechanistic Investigation of a Silylation-Based Kinetic Resolution Using Linear Free Energy Relationships and Its Application to Substrate Expansion and Polymer Supported Kinetic Resolutions. [Internet] [Doctoral dissertation]. University of South Carolina; 2014. [cited 2019 Jun 17]. Available from: https://scholarcommons.sc.edu/etd/2785.

Council of Science Editors:

AKHANI RK. Mechanistic Investigation of a Silylation-Based Kinetic Resolution Using Linear Free Energy Relationships and Its Application to Substrate Expansion and Polymer Supported Kinetic Resolutions. [Doctoral Dissertation]. University of South Carolina; 2014. Available from: https://scholarcommons.sc.edu/etd/2785

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