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You searched for +publisher:"University of Texas – Austin" +contributor:("Liu, Hung-Wen"). Showing records 1 – 30 of 37 total matches.

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University of Texas – Austin

1. Kim, Nam Ho, 1975-. Mechanistic investigations of SpnF- and SpnL-catalyzed cyclizations in the biosynthesis of spinosyn A.

Degree: PhD, Pharmacy, 2013, University of Texas – Austin

 Spinosyn A is a particularly interesting natural product due to its structural complexity and potent insecticidal activity. The biosynthetic pathway of spinosyn A is interesting… (more)

Subjects/Keywords: Spinosyn A; Cyclization; Cycloaddition; SpnF; SpnL; Mechanism; Diels-Alder; Rauhut-Currier; Kinetic isotope effect; Mechanism-based inhibitor

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APA (6th Edition):

Kim, Nam Ho, 1. (2013). Mechanistic investigations of SpnF- and SpnL-catalyzed cyclizations in the biosynthesis of spinosyn A. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/28735

Chicago Manual of Style (16th Edition):

Kim, Nam Ho, 1975-. “Mechanistic investigations of SpnF- and SpnL-catalyzed cyclizations in the biosynthesis of spinosyn A.” 2013. Doctoral Dissertation, University of Texas – Austin. Accessed September 23, 2019. http://hdl.handle.net/2152/28735.

MLA Handbook (7th Edition):

Kim, Nam Ho, 1975-. “Mechanistic investigations of SpnF- and SpnL-catalyzed cyclizations in the biosynthesis of spinosyn A.” 2013. Web. 23 Sep 2019.

Vancouver:

Kim, Nam Ho 1. Mechanistic investigations of SpnF- and SpnL-catalyzed cyclizations in the biosynthesis of spinosyn A. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2013. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/2152/28735.

Council of Science Editors:

Kim, Nam Ho 1. Mechanistic investigations of SpnF- and SpnL-catalyzed cyclizations in the biosynthesis of spinosyn A. [Doctoral Dissertation]. University of Texas – Austin; 2013. Available from: http://hdl.handle.net/2152/28735


University of Texas – Austin

2. Thibodeaux, Christopher James. Mechanistic studies of two enzymes that employ common coenzymes in uncommon ways.

Degree: PhD, Cell and Molecular Biology, 2010, University of Texas – Austin

 Enzymes are biological catalysts which greatly accelerate the rates of chemical reactions, oftentimes by many orders of magnitude over the uncatalyzed reaction. The remarkable catalytic… (more)

Subjects/Keywords: Enzyme catalysis; Isoprenoid biosynthesis; IDI-2; ACCD; Chemical mechanism

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APA (6th Edition):

Thibodeaux, C. J. (2010). Mechanistic studies of two enzymes that employ common coenzymes in uncommon ways. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/22160

Chicago Manual of Style (16th Edition):

Thibodeaux, Christopher James. “Mechanistic studies of two enzymes that employ common coenzymes in uncommon ways.” 2010. Doctoral Dissertation, University of Texas – Austin. Accessed September 23, 2019. http://hdl.handle.net/2152/22160.

MLA Handbook (7th Edition):

Thibodeaux, Christopher James. “Mechanistic studies of two enzymes that employ common coenzymes in uncommon ways.” 2010. Web. 23 Sep 2019.

Vancouver:

Thibodeaux CJ. Mechanistic studies of two enzymes that employ common coenzymes in uncommon ways. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2010. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/2152/22160.

Council of Science Editors:

Thibodeaux CJ. Mechanistic studies of two enzymes that employ common coenzymes in uncommon ways. [Doctoral Dissertation]. University of Texas – Austin; 2010. Available from: http://hdl.handle.net/2152/22160


University of Texas – Austin

3. Choi, Sei Hyun. Synthetic approaches to investigate the chemical mechanism in the biosynthesis of natural products.

Degree: PhD, Chemistry, 2012, University of Texas – Austin

 The study of the biosynthetic logic of natural products has established itself to be one of the more exciting areas of research and have become… (more)

Subjects/Keywords: Natural product; Chemical mechanism; Organic synthesis; Spinosyn; Diels-Alder reaction; Rauhut-Currier reaction; Apiose; AXS; Desii; Radical SAM enzyme

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APA (6th Edition):

Choi, S. H. (2012). Synthetic approaches to investigate the chemical mechanism in the biosynthesis of natural products. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/26079

Chicago Manual of Style (16th Edition):

Choi, Sei Hyun. “Synthetic approaches to investigate the chemical mechanism in the biosynthesis of natural products.” 2012. Doctoral Dissertation, University of Texas – Austin. Accessed September 23, 2019. http://hdl.handle.net/2152/26079.

MLA Handbook (7th Edition):

Choi, Sei Hyun. “Synthetic approaches to investigate the chemical mechanism in the biosynthesis of natural products.” 2012. Web. 23 Sep 2019.

Vancouver:

Choi SH. Synthetic approaches to investigate the chemical mechanism in the biosynthesis of natural products. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2012. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/2152/26079.

Council of Science Editors:

Choi SH. Synthetic approaches to investigate the chemical mechanism in the biosynthesis of natural products. [Doctoral Dissertation]. University of Texas – Austin; 2012. Available from: http://hdl.handle.net/2152/26079

4. Kim, Hak Joong, 1974-. Investigation of the post-polyketide synthase (PKS) modifications during spinosyn A biosynthesis in Saccharopolyspora spinosa.

Degree: PhD, Chemistry, 2010, University of Texas – Austin

 Diverse biological activities of polyketide natural products are often associated with specific structural motifs, biosynthetically introduced after construction of the polyketide core. Therefore, investigation of… (more)

Subjects/Keywords: Polyketide; Biosynthesis; Spinosyn; Methyltransferase; Diels-Alderase; Rauhut-Currier reaction; Intramolecular C-C bond formation; Kinetics; Enzyme mechanism

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APA (6th Edition):

Kim, Hak Joong, 1. (2010). Investigation of the post-polyketide synthase (PKS) modifications during spinosyn A biosynthesis in Saccharopolyspora spinosa. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/22143

Chicago Manual of Style (16th Edition):

Kim, Hak Joong, 1974-. “Investigation of the post-polyketide synthase (PKS) modifications during spinosyn A biosynthesis in Saccharopolyspora spinosa.” 2010. Doctoral Dissertation, University of Texas – Austin. Accessed September 23, 2019. http://hdl.handle.net/2152/22143.

MLA Handbook (7th Edition):

Kim, Hak Joong, 1974-. “Investigation of the post-polyketide synthase (PKS) modifications during spinosyn A biosynthesis in Saccharopolyspora spinosa.” 2010. Web. 23 Sep 2019.

Vancouver:

Kim, Hak Joong 1. Investigation of the post-polyketide synthase (PKS) modifications during spinosyn A biosynthesis in Saccharopolyspora spinosa. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2010. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/2152/22143.

Council of Science Editors:

Kim, Hak Joong 1. Investigation of the post-polyketide synthase (PKS) modifications during spinosyn A biosynthesis in Saccharopolyspora spinosa. [Doctoral Dissertation]. University of Texas – Austin; 2010. Available from: http://hdl.handle.net/2152/22143

5. Zhou, Ying, 1977-. Studies of the metal binding properties and DNA recognition mode of the unusual zinc fingers in poly(ADP-ribose) Polymerase-1 and the investigation of its interaction with apoptosis inducing factor (AIF).

Degree: PhD, Cell and Molecular Biology, 2009, University of Texas – Austin

 Poly(ADP-ribosyl)ation, a covalent modification of proteins catalyzed by poly(ADP-ribose) polymerases (PARPs), plays a crucial role in regulating DNA repair, DNA replication, and cell death. Poly(ADP-ribose)… (more)

Subjects/Keywords: DNA repair; Poly(ADP-ribosyl)ation; Poly(ADP-ribose) polymerases; Poly(ADP-ribose) Polymerase-1; Zinc fingers; PARP; DNA-binding protein; DNA-binding properties; Apoptosis

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APA (6th Edition):

Zhou, Ying, 1. (2009). Studies of the metal binding properties and DNA recognition mode of the unusual zinc fingers in poly(ADP-ribose) Polymerase-1 and the investigation of its interaction with apoptosis inducing factor (AIF). (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/21906

Chicago Manual of Style (16th Edition):

Zhou, Ying, 1977-. “Studies of the metal binding properties and DNA recognition mode of the unusual zinc fingers in poly(ADP-ribose) Polymerase-1 and the investigation of its interaction with apoptosis inducing factor (AIF).” 2009. Doctoral Dissertation, University of Texas – Austin. Accessed September 23, 2019. http://hdl.handle.net/2152/21906.

MLA Handbook (7th Edition):

Zhou, Ying, 1977-. “Studies of the metal binding properties and DNA recognition mode of the unusual zinc fingers in poly(ADP-ribose) Polymerase-1 and the investigation of its interaction with apoptosis inducing factor (AIF).” 2009. Web. 23 Sep 2019.

Vancouver:

Zhou, Ying 1. Studies of the metal binding properties and DNA recognition mode of the unusual zinc fingers in poly(ADP-ribose) Polymerase-1 and the investigation of its interaction with apoptosis inducing factor (AIF). [Internet] [Doctoral dissertation]. University of Texas – Austin; 2009. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/2152/21906.

Council of Science Editors:

Zhou, Ying 1. Studies of the metal binding properties and DNA recognition mode of the unusual zinc fingers in poly(ADP-ribose) Polymerase-1 and the investigation of its interaction with apoptosis inducing factor (AIF). [Doctoral Dissertation]. University of Texas – Austin; 2009. Available from: http://hdl.handle.net/2152/21906


University of Texas – Austin

6. Wagner, Drew Taylor. Structural and functional studies of uncommon polyketide synthase domains.

Degree: PhD, Biochemistry, 2017, University of Texas – Austin

 Over the past 4 billion years or so, beginning in the primordial soup from which terrestrial life descends, Mother Nature has been molding matter into… (more)

Subjects/Keywords: Polyketide; Protein crystallography; Biochemistry; Biosynthesis

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APA (6th Edition):

Wagner, D. T. (2017). Structural and functional studies of uncommon polyketide synthase domains. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/68146

Chicago Manual of Style (16th Edition):

Wagner, Drew Taylor. “Structural and functional studies of uncommon polyketide synthase domains.” 2017. Doctoral Dissertation, University of Texas – Austin. Accessed September 23, 2019. http://hdl.handle.net/2152/68146.

MLA Handbook (7th Edition):

Wagner, Drew Taylor. “Structural and functional studies of uncommon polyketide synthase domains.” 2017. Web. 23 Sep 2019.

Vancouver:

Wagner DT. Structural and functional studies of uncommon polyketide synthase domains. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2017. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/2152/68146.

Council of Science Editors:

Wagner DT. Structural and functional studies of uncommon polyketide synthase domains. [Doctoral Dissertation]. University of Texas – Austin; 2017. Available from: http://hdl.handle.net/2152/68146


University of Texas – Austin

7. White-Phillip, Jessica Ann. Glycosylation reactions in secondary metabolism : glycosylation events in C-mannosylation and the biosynthesis of kijanimicin.

Degree: PhD, Cell and Molecular Biology, 2010, University of Texas – Austin

 In this work, we examine two disparate aspects of glycosylation. The first project involves the elucidation of the glycosylation of the novel tetronolide natural product,… (more)

Subjects/Keywords: C-mannosylation; Kijanimicin glycosylation; TDP-L-digitoxose

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APA (6th Edition):

White-Phillip, J. A. (2010). Glycosylation reactions in secondary metabolism : glycosylation events in C-mannosylation and the biosynthesis of kijanimicin. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/30539

Chicago Manual of Style (16th Edition):

White-Phillip, Jessica Ann. “Glycosylation reactions in secondary metabolism : glycosylation events in C-mannosylation and the biosynthesis of kijanimicin.” 2010. Doctoral Dissertation, University of Texas – Austin. Accessed September 23, 2019. http://hdl.handle.net/2152/30539.

MLA Handbook (7th Edition):

White-Phillip, Jessica Ann. “Glycosylation reactions in secondary metabolism : glycosylation events in C-mannosylation and the biosynthesis of kijanimicin.” 2010. Web. 23 Sep 2019.

Vancouver:

White-Phillip JA. Glycosylation reactions in secondary metabolism : glycosylation events in C-mannosylation and the biosynthesis of kijanimicin. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2010. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/2152/30539.

Council of Science Editors:

White-Phillip JA. Glycosylation reactions in secondary metabolism : glycosylation events in C-mannosylation and the biosynthesis of kijanimicin. [Doctoral Dissertation]. University of Texas – Austin; 2010. Available from: http://hdl.handle.net/2152/30539


University of Texas – Austin

8. Lim, Byung Joon (Ph. D. in chemistry). Synthesis and application of electrochemically active oligonucleotides.

Degree: PhD, Chemistry, 2019, University of Texas – Austin

 Modified oligonucleotides with redox-active functional groups could emerge as attractive tools for sensor development. In principle, changes in oligonucleotide hybridization or conformation may be read… (more)

Subjects/Keywords: Modified oligonucleotide; Ferrocene; Electrochemical detection; E-sensor; Ratiomatric sensor

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APA (6th Edition):

Lim, B. J. (. D. i. c. (2019). Synthesis and application of electrochemically active oligonucleotides. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/2668

Chicago Manual of Style (16th Edition):

Lim, Byung Joon (Ph D in chemistry). “Synthesis and application of electrochemically active oligonucleotides.” 2019. Doctoral Dissertation, University of Texas – Austin. Accessed September 23, 2019. http://dx.doi.org/10.26153/tsw/2668.

MLA Handbook (7th Edition):

Lim, Byung Joon (Ph D in chemistry). “Synthesis and application of electrochemically active oligonucleotides.” 2019. Web. 23 Sep 2019.

Vancouver:

Lim BJ(Dic. Synthesis and application of electrochemically active oligonucleotides. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2019. [cited 2019 Sep 23]. Available from: http://dx.doi.org/10.26153/tsw/2668.

Council of Science Editors:

Lim BJ(Dic. Synthesis and application of electrochemically active oligonucleotides. [Doctoral Dissertation]. University of Texas – Austin; 2019. Available from: http://dx.doi.org/10.26153/tsw/2668


University of Texas – Austin

9. -7981-5709. Rhodium(I)-catalyzed C–C bond activation : decarbonylation of α,β-acetylenic ketones: Rhodium(I)-catalyzed C–C bond activation : decarbonylation of [alpha], [beta]-acetylenic ketones.

Degree: PhD, Chemistry, 2016, University of Texas – Austin

 Transition metal-catalyzed carbon–carbon (C–C) bond activation is a useful way to construct organic molecules that could be difficult or impossible to achieve under traditional synthetic… (more)

Subjects/Keywords: Carbon-alkyne activation; Decarbonylation; Ynone

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APA (6th Edition):

-7981-5709. (2016). Rhodium(I)-catalyzed C–C bond activation : decarbonylation of α,β-acetylenic ketones: Rhodium(I)-catalyzed C–C bond activation : decarbonylation of [alpha], [beta]-acetylenic ketones. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/40932

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Chicago Manual of Style (16th Edition):

-7981-5709. “Rhodium(I)-catalyzed C–C bond activation : decarbonylation of α,β-acetylenic ketones: Rhodium(I)-catalyzed C–C bond activation : decarbonylation of [alpha], [beta]-acetylenic ketones.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed September 23, 2019. http://hdl.handle.net/2152/40932.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

-7981-5709. “Rhodium(I)-catalyzed C–C bond activation : decarbonylation of α,β-acetylenic ketones: Rhodium(I)-catalyzed C–C bond activation : decarbonylation of [alpha], [beta]-acetylenic ketones.” 2016. Web. 23 Sep 2019.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

-7981-5709. Rhodium(I)-catalyzed C–C bond activation : decarbonylation of α,β-acetylenic ketones: Rhodium(I)-catalyzed C–C bond activation : decarbonylation of [alpha], [beta]-acetylenic ketones. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/2152/40932.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

-7981-5709. Rhodium(I)-catalyzed C–C bond activation : decarbonylation of α,β-acetylenic ketones: Rhodium(I)-catalyzed C–C bond activation : decarbonylation of [alpha], [beta]-acetylenic ketones. [Doctoral Dissertation]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/40932

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete


University of Texas – Austin

10. -3503-3219. Syntheses of anticancer agents that target DNA : steroids, nucleosides, and platinums.

Degree: PhD, Pharmaceutical Sciences, 2017, University of Texas – Austin

 Cephalostatins from Cephalodiscus gilchristi and ritterazines from Ritterella tokioka inhibit cell growth in nanomolar concentrations by inducing unknown apoptosis pathway. Their NCI-60 growth inhibition patterns… (more)

Subjects/Keywords: Cephalostatin; Ritterazine; EZH2; 7-Deazaguanine; DNA repair; Platinum-intercalator conjugate; Interstrand crosslink

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APA (6th Edition):

-3503-3219. (2017). Syntheses of anticancer agents that target DNA : steroids, nucleosides, and platinums. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/72692

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Chicago Manual of Style (16th Edition):

-3503-3219. “Syntheses of anticancer agents that target DNA : steroids, nucleosides, and platinums.” 2017. Doctoral Dissertation, University of Texas – Austin. Accessed September 23, 2019. http://hdl.handle.net/2152/72692.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

-3503-3219. “Syntheses of anticancer agents that target DNA : steroids, nucleosides, and platinums.” 2017. Web. 23 Sep 2019.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

-3503-3219. Syntheses of anticancer agents that target DNA : steroids, nucleosides, and platinums. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2017. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/2152/72692.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

-3503-3219. Syntheses of anticancer agents that target DNA : steroids, nucleosides, and platinums. [Doctoral Dissertation]. University of Texas – Austin; 2017. Available from: http://hdl.handle.net/2152/72692

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete


University of Texas – Austin

11. Wu, Meilan. DNA recognition and mechanistic investigation of poly(ADP-ribose) polymerase-1.

Degree: PhD, Pharmaceutical Sciences, 2014, University of Texas – Austin

 Human PARP-1 is a nuclear protein containing six functional domains that catalyzes the poly(ADP-ribosyl)ation of a variety of protein substrates including itself. This process involves… (more)

Subjects/Keywords: Poly(ADP-ribosyl)ation; PARP-1

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APA (6th Edition):

Wu, M. (2014). DNA recognition and mechanistic investigation of poly(ADP-ribose) polymerase-1. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/62238

Chicago Manual of Style (16th Edition):

Wu, Meilan. “DNA recognition and mechanistic investigation of poly(ADP-ribose) polymerase-1.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed September 23, 2019. http://hdl.handle.net/2152/62238.

MLA Handbook (7th Edition):

Wu, Meilan. “DNA recognition and mechanistic investigation of poly(ADP-ribose) polymerase-1.” 2014. Web. 23 Sep 2019.

Vancouver:

Wu M. DNA recognition and mechanistic investigation of poly(ADP-ribose) polymerase-1. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/2152/62238.

Council of Science Editors:

Wu M. DNA recognition and mechanistic investigation of poly(ADP-ribose) polymerase-1. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/62238


University of Texas – Austin

12. Luong, Tom Tuan. Development of transition metal catalyzed carbon-carbon bond forming reactions with abundant or scarce chemicals.

Degree: PhD, Chemistry, 2017, University of Texas – Austin

 The development of more efficient carbon-carbon bond transformation is of great significance. One of the more common approaches to forging carbon-carbon bonds is the addition… (more)

Subjects/Keywords: Transfer hydrogenation

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APA (6th Edition):

Luong, T. T. (2017). Development of transition metal catalyzed carbon-carbon bond forming reactions with abundant or scarce chemicals. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/61785

Chicago Manual of Style (16th Edition):

Luong, Tom Tuan. “Development of transition metal catalyzed carbon-carbon bond forming reactions with abundant or scarce chemicals.” 2017. Doctoral Dissertation, University of Texas – Austin. Accessed September 23, 2019. http://hdl.handle.net/2152/61785.

MLA Handbook (7th Edition):

Luong, Tom Tuan. “Development of transition metal catalyzed carbon-carbon bond forming reactions with abundant or scarce chemicals.” 2017. Web. 23 Sep 2019.

Vancouver:

Luong TT. Development of transition metal catalyzed carbon-carbon bond forming reactions with abundant or scarce chemicals. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2017. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/2152/61785.

Council of Science Editors:

Luong TT. Development of transition metal catalyzed carbon-carbon bond forming reactions with abundant or scarce chemicals. [Doctoral Dissertation]. University of Texas – Austin; 2017. Available from: http://hdl.handle.net/2152/61785


University of Texas – Austin

13. -3473-3494. Total syntheses of the regenerative natural products vinaxanthone, xanthofulvin, and eupalinilide E.

Degree: PhD, Chemistry, 2015, University of Texas – Austin

 The fungal metabolites vinaxanthone and xanthofulvin possess the remarkable ability to restore motor function in animal models of complete spinal cord transection making them the… (more)

Subjects/Keywords: Regenerative natural products; Vinaxanthone; Xanthofulvin; Eupalinilide E

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APA (6th Edition):

-3473-3494. (2015). Total syntheses of the regenerative natural products vinaxanthone, xanthofulvin, and eupalinilide E. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/30456

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Chicago Manual of Style (16th Edition):

-3473-3494. “Total syntheses of the regenerative natural products vinaxanthone, xanthofulvin, and eupalinilide E.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed September 23, 2019. http://hdl.handle.net/2152/30456.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

-3473-3494. “Total syntheses of the regenerative natural products vinaxanthone, xanthofulvin, and eupalinilide E.” 2015. Web. 23 Sep 2019.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

-3473-3494. Total syntheses of the regenerative natural products vinaxanthone, xanthofulvin, and eupalinilide E. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/2152/30456.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

-3473-3494. Total syntheses of the regenerative natural products vinaxanthone, xanthofulvin, and eupalinilide E. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/30456

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete


University of Texas – Austin

14. Ko, Yeonjin. Unusual carbohydrate biosynthesis : mechanistic studies of DesII and the biosynthesis of formycin A.

Degree: PhD, Chemistry, 2017, University of Texas – Austin

 Carbohydrates are essential biomolecules in all living organisms. Besides serving as energy storage and structural building blocks in primary metabolism, carbohydrates represent the building blocks… (more)

Subjects/Keywords: DesII; Formycin; Formycin A; Carbohydrate biosynthesis; Biosynthetic pathways; Radical intermediates

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APA (6th Edition):

Ko, Y. (2017). Unusual carbohydrate biosynthesis : mechanistic studies of DesII and the biosynthesis of formycin A. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/47151

Chicago Manual of Style (16th Edition):

Ko, Yeonjin. “Unusual carbohydrate biosynthesis : mechanistic studies of DesII and the biosynthesis of formycin A.” 2017. Doctoral Dissertation, University of Texas – Austin. Accessed September 23, 2019. http://hdl.handle.net/2152/47151.

MLA Handbook (7th Edition):

Ko, Yeonjin. “Unusual carbohydrate biosynthesis : mechanistic studies of DesII and the biosynthesis of formycin A.” 2017. Web. 23 Sep 2019.

Vancouver:

Ko Y. Unusual carbohydrate biosynthesis : mechanistic studies of DesII and the biosynthesis of formycin A. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2017. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/2152/47151.

Council of Science Editors:

Ko Y. Unusual carbohydrate biosynthesis : mechanistic studies of DesII and the biosynthesis of formycin A. [Doctoral Dissertation]. University of Texas – Austin; 2017. Available from: http://hdl.handle.net/2152/47151


University of Texas – Austin

15. -7139-2043. Structural and kinetic study of N7-methyl, N7-benzyl and C8-chloro guanine lesions using human DNA polymerase β: Structural and kinetic study of N7-methyl, N7-benzyl and C8-chloro guanine lesions using human DNA polymerase [beta].

Degree: PhD, Biochemistry, 2015, University of Texas – Austin

 DNA bases are constantly under the damages from both outside and inside, bringing possible mutagenic changes. To elucidate the detailed mechanisms, structural method of X-ray… (more)

Subjects/Keywords: N7-methyl; N7-benzyl; C8-chloro; Guanine lesions; Human DNA polymerase β

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APA (6th Edition):

-7139-2043. (2015). Structural and kinetic study of N7-methyl, N7-benzyl and C8-chloro guanine lesions using human DNA polymerase β: Structural and kinetic study of N7-methyl, N7-benzyl and C8-chloro guanine lesions using human DNA polymerase [beta]. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/46815

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-7139-2043. “Structural and kinetic study of N7-methyl, N7-benzyl and C8-chloro guanine lesions using human DNA polymerase β: Structural and kinetic study of N7-methyl, N7-benzyl and C8-chloro guanine lesions using human DNA polymerase [beta].” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed September 23, 2019. http://hdl.handle.net/2152/46815.

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Author name may be incomplete

MLA Handbook (7th Edition):

-7139-2043. “Structural and kinetic study of N7-methyl, N7-benzyl and C8-chloro guanine lesions using human DNA polymerase β: Structural and kinetic study of N7-methyl, N7-benzyl and C8-chloro guanine lesions using human DNA polymerase [beta].” 2015. Web. 23 Sep 2019.

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Author name may be incomplete

Vancouver:

-7139-2043. Structural and kinetic study of N7-methyl, N7-benzyl and C8-chloro guanine lesions using human DNA polymerase β: Structural and kinetic study of N7-methyl, N7-benzyl and C8-chloro guanine lesions using human DNA polymerase [beta]. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/2152/46815.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

-7139-2043. Structural and kinetic study of N7-methyl, N7-benzyl and C8-chloro guanine lesions using human DNA polymerase β: Structural and kinetic study of N7-methyl, N7-benzyl and C8-chloro guanine lesions using human DNA polymerase [beta]. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/46815

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Author name may be incomplete


University of Texas – Austin

16. -1902-3184. Transition metal catalyzed redox triggered C–C bond forming reactions of alcohols via transfer hydrogenation.

Degree: PhD, Chemistry, 2016, University of Texas – Austin

 Carbonyl addition is one of the fundamental reactions forming C–C bonds in organic chemistry to construct structurally complex organic molecules, in particular natural products, from… (more)

Subjects/Keywords: C–C bond forming reaction; Transition metal catalysis; Transfer hydrogenation

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APA (6th Edition):

-1902-3184. (2016). Transition metal catalyzed redox triggered C–C bond forming reactions of alcohols via transfer hydrogenation. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/46996

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-1902-3184. “Transition metal catalyzed redox triggered C–C bond forming reactions of alcohols via transfer hydrogenation.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed September 23, 2019. http://hdl.handle.net/2152/46996.

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Author name may be incomplete

MLA Handbook (7th Edition):

-1902-3184. “Transition metal catalyzed redox triggered C–C bond forming reactions of alcohols via transfer hydrogenation.” 2016. Web. 23 Sep 2019.

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Author name may be incomplete

Vancouver:

-1902-3184. Transition metal catalyzed redox triggered C–C bond forming reactions of alcohols via transfer hydrogenation. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/2152/46996.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

-1902-3184. Transition metal catalyzed redox triggered C–C bond forming reactions of alcohols via transfer hydrogenation. [Doctoral Dissertation]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/46996

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Author name may be incomplete


University of Texas – Austin

17. -2419-9854. Development of neutral redox carbon-carbon bond forming reactions via transition metal-catalyzed transfer hydrogenation.

Degree: PhD, Chemistry, 2018, University of Texas – Austin

 Since C–C bonds form the backbone of every organic molecule and reside at the heart of chemical science, the development of new efficient methods for… (more)

Subjects/Keywords: Neutral redox; Transfer hydrogenation; C–C couplings

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APA (6th Edition):

-2419-9854. (2018). Development of neutral redox carbon-carbon bond forming reactions via transition metal-catalyzed transfer hydrogenation. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/63343

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-2419-9854. “Development of neutral redox carbon-carbon bond forming reactions via transition metal-catalyzed transfer hydrogenation.” 2018. Doctoral Dissertation, University of Texas – Austin. Accessed September 23, 2019. http://hdl.handle.net/2152/63343.

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Author name may be incomplete

MLA Handbook (7th Edition):

-2419-9854. “Development of neutral redox carbon-carbon bond forming reactions via transition metal-catalyzed transfer hydrogenation.” 2018. Web. 23 Sep 2019.

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Author name may be incomplete

Vancouver:

-2419-9854. Development of neutral redox carbon-carbon bond forming reactions via transition metal-catalyzed transfer hydrogenation. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2018. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/2152/63343.

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Author name may be incomplete

Council of Science Editors:

-2419-9854. Development of neutral redox carbon-carbon bond forming reactions via transition metal-catalyzed transfer hydrogenation. [Doctoral Dissertation]. University of Texas – Austin; 2018. Available from: http://hdl.handle.net/2152/63343

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University of Texas – Austin

18. -9758-983X. The design of halopyridine-based activity-based probes and mechanistic studies of succinylarginine dihydrolase.

Degree: PhD, Pharmaceutical Sciences, 2015, University of Texas – Austin

 An important design aspect of covalent inactivators is the balance between reactivity, or reversibility of reaction, with nucleophiles in solution and reactivity with nucleophiles at… (more)

Subjects/Keywords: Dimethylarginine dimethylaminohydrolase; Halopyridine; Activity-based probes; Succinylarginine dihydrolase

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APA (6th Edition):

-9758-983X. (2015). The design of halopyridine-based activity-based probes and mechanistic studies of succinylarginine dihydrolase. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/46556

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-9758-983X. “The design of halopyridine-based activity-based probes and mechanistic studies of succinylarginine dihydrolase.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed September 23, 2019. http://hdl.handle.net/2152/46556.

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Author name may be incomplete

MLA Handbook (7th Edition):

-9758-983X. “The design of halopyridine-based activity-based probes and mechanistic studies of succinylarginine dihydrolase.” 2015. Web. 23 Sep 2019.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

-9758-983X. The design of halopyridine-based activity-based probes and mechanistic studies of succinylarginine dihydrolase. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/2152/46556.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

-9758-983X. The design of halopyridine-based activity-based probes and mechanistic studies of succinylarginine dihydrolase. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/46556

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Author name may be incomplete


University of Texas – Austin

19. Sun, He, Ph. D. Studies of unusual catalysis : a tale of four enzymes from diverse biosynthesis pathways.

Degree: PhD, Pharmaceutical Sciences, 2013, University of Texas – Austin

 The diverse reactions that enzymes catalyze have fascinated enzymologists for decades. Continuing investigations in the biosynthesis of both primary and secondary metabolites have led to… (more)

Subjects/Keywords: Unusual; Catalysis; Enzyme; Biosynthesis; Mechanism; Characterization; UDP-galactopyranose mutase; Sulfur carrier protein activating enzyme; Cobalamin-dependent radical S-adenosyl-L-methionine enzymes

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APA (6th Edition):

Sun, He, P. D. (2013). Studies of unusual catalysis : a tale of four enzymes from diverse biosynthesis pathways. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/63875

Chicago Manual of Style (16th Edition):

Sun, He, Ph D. “Studies of unusual catalysis : a tale of four enzymes from diverse biosynthesis pathways.” 2013. Doctoral Dissertation, University of Texas – Austin. Accessed September 23, 2019. http://hdl.handle.net/2152/63875.

MLA Handbook (7th Edition):

Sun, He, Ph D. “Studies of unusual catalysis : a tale of four enzymes from diverse biosynthesis pathways.” 2013. Web. 23 Sep 2019.

Vancouver:

Sun, He PD. Studies of unusual catalysis : a tale of four enzymes from diverse biosynthesis pathways. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2013. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/2152/63875.

Council of Science Editors:

Sun, He PD. Studies of unusual catalysis : a tale of four enzymes from diverse biosynthesis pathways. [Doctoral Dissertation]. University of Texas – Austin; 2013. Available from: http://hdl.handle.net/2152/63875


University of Texas – Austin

20. Lin, Chia-I. Biosynthetic studies of lincomycin A, a thiosugar-containing natural product.

Degree: PhD, Chemistry, 2019, University of Texas – Austin

 The dissertation describes biosynthetic studies of lincomycin A, a thiosugarcontaining natural product. Lincomycin A was isolated from Streptomyces lincolnensis and has been used clinically as… (more)

Subjects/Keywords: Biosynthesis; Lincomycin; Thiosugar

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APA (6th Edition):

Lin, C. (2019). Biosynthetic studies of lincomycin A, a thiosugar-containing natural product. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/2237

Chicago Manual of Style (16th Edition):

Lin, Chia-I. “Biosynthetic studies of lincomycin A, a thiosugar-containing natural product.” 2019. Doctoral Dissertation, University of Texas – Austin. Accessed September 23, 2019. http://dx.doi.org/10.26153/tsw/2237.

MLA Handbook (7th Edition):

Lin, Chia-I. “Biosynthetic studies of lincomycin A, a thiosugar-containing natural product.” 2019. Web. 23 Sep 2019.

Vancouver:

Lin C. Biosynthetic studies of lincomycin A, a thiosugar-containing natural product. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2019. [cited 2019 Sep 23]. Available from: http://dx.doi.org/10.26153/tsw/2237.

Council of Science Editors:

Lin C. Biosynthetic studies of lincomycin A, a thiosugar-containing natural product. [Doctoral Dissertation]. University of Texas – Austin; 2019. Available from: http://dx.doi.org/10.26153/tsw/2237


University of Texas – Austin

21. Jo, Hyun Hwa. Optical chirality sensing ensembles : mechanistic studies and applications in synthetic methodology development.

Degree: PhD, Chemistry, 2015, University of Texas – Austin

 In the pharmaceutical industry, the development of molecular or chemical sensors for an analyte of interest and the determination of the enantiomeric purity of chiral… (more)

Subjects/Keywords: Optical ee sensing; High-throughput ee sensing; Enantiomeric excess; Enantiomeric excess analysis; ee analysis; ee screening; Chirality sensing; Multi-component assembly reaction; Chiral ketones; Synthetic methodology

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APA (6th Edition):

Jo, H. H. (2015). Optical chirality sensing ensembles : mechanistic studies and applications in synthetic methodology development. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/46977

Chicago Manual of Style (16th Edition):

Jo, Hyun Hwa. “Optical chirality sensing ensembles : mechanistic studies and applications in synthetic methodology development.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed September 23, 2019. http://hdl.handle.net/2152/46977.

MLA Handbook (7th Edition):

Jo, Hyun Hwa. “Optical chirality sensing ensembles : mechanistic studies and applications in synthetic methodology development.” 2015. Web. 23 Sep 2019.

Vancouver:

Jo HH. Optical chirality sensing ensembles : mechanistic studies and applications in synthetic methodology development. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/2152/46977.

Council of Science Editors:

Jo HH. Optical chirality sensing ensembles : mechanistic studies and applications in synthetic methodology development. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/46977


University of Texas – Austin

22. Zamora Olivares, Diana Paulina. Differential sensing of kinases.

Degree: PhD, Organic Chemistry, 2014, University of Texas – Austin

 During the last decade, organic and supramolecular chemistry in combination with analytical and fluorescent-based sensing methods have led to the development of chemical biology tools… (more)

Subjects/Keywords: Chemosensors; Kinases

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APA (6th Edition):

Zamora Olivares, D. P. (2014). Differential sensing of kinases. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/30454

Chicago Manual of Style (16th Edition):

Zamora Olivares, Diana Paulina. “Differential sensing of kinases.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed September 23, 2019. http://hdl.handle.net/2152/30454.

MLA Handbook (7th Edition):

Zamora Olivares, Diana Paulina. “Differential sensing of kinases.” 2014. Web. 23 Sep 2019.

Vancouver:

Zamora Olivares DP. Differential sensing of kinases. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/2152/30454.

Council of Science Editors:

Zamora Olivares DP. Differential sensing of kinases. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/30454


University of Texas – Austin

23. -4830-8963. Supramolecular chemistry of functionalized "Texas-sized" molecular boxes and their applications in hydrogel materials.

Degree: PhD, Chemistry, 2018, University of Texas – Austin

 Positively-charged, electron-deficient, and box-like macrocyclic receptors, such as “the blue box” (CBPQT⁴⁺) and its diversiform congeners, have been widely recognized for their roles in the… (more)

Subjects/Keywords: Texas-sized molecular boxes; Self-assembly; Anion recognition

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APA (6th Edition):

-4830-8963. (2018). Supramolecular chemistry of functionalized "Texas-sized" molecular boxes and their applications in hydrogel materials. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/65669

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Chicago Manual of Style (16th Edition):

-4830-8963. “Supramolecular chemistry of functionalized "Texas-sized" molecular boxes and their applications in hydrogel materials.” 2018. Doctoral Dissertation, University of Texas – Austin. Accessed September 23, 2019. http://hdl.handle.net/2152/65669.

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Author name may be incomplete

MLA Handbook (7th Edition):

-4830-8963. “Supramolecular chemistry of functionalized "Texas-sized" molecular boxes and their applications in hydrogel materials.” 2018. Web. 23 Sep 2019.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

-4830-8963. Supramolecular chemistry of functionalized "Texas-sized" molecular boxes and their applications in hydrogel materials. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2018. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/2152/65669.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

-4830-8963. Supramolecular chemistry of functionalized "Texas-sized" molecular boxes and their applications in hydrogel materials. [Doctoral Dissertation]. University of Texas – Austin; 2018. Available from: http://hdl.handle.net/2152/65669

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University of Texas – Austin

24. Ren, Zhi. Palladium-catalyzed carbon-hydrogen bond functionalization utilizing an exo-directing strategy.

Degree: PhD, Chemistry, 2016, University of Texas – Austin

 Transition metal catalyzed functionalization of carbon-hydrogen bonds (C−H bonds) has become an exponentially growing field. Particularly, Pd-catalyzed methods with various directing groups (DGs) have been… (more)

Subjects/Keywords: C-H activation; C-H functionalization; Palladium catalysis

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APA (6th Edition):

Ren, Z. (2016). Palladium-catalyzed carbon-hydrogen bond functionalization utilizing an exo-directing strategy. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/39758

Chicago Manual of Style (16th Edition):

Ren, Zhi. “Palladium-catalyzed carbon-hydrogen bond functionalization utilizing an exo-directing strategy.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed September 23, 2019. http://hdl.handle.net/2152/39758.

MLA Handbook (7th Edition):

Ren, Zhi. “Palladium-catalyzed carbon-hydrogen bond functionalization utilizing an exo-directing strategy.” 2016. Web. 23 Sep 2019.

Vancouver:

Ren Z. Palladium-catalyzed carbon-hydrogen bond functionalization utilizing an exo-directing strategy. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/2152/39758.

Council of Science Editors:

Ren Z. Palladium-catalyzed carbon-hydrogen bond functionalization utilizing an exo-directing strategy. [Doctoral Dissertation]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/39758


University of Texas – Austin

25. Lee, Juhoon. Syntheses of calix[4]pyrrole functionalized extended molecular systems and applications for environmental concerns.

Degree: PhD, Chemistry, 2017, University of Texas – Austin

 Considerable efforts have been made to develop the supramolecular systems being capable of selectively binding and recognizing specific chemical species. Within this context, particular has… (more)

Subjects/Keywords: Metal-organic frameworks; Calix[4]pyrrole; Cage

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APA (6th Edition):

Lee, J. (2017). Syntheses of calix[4]pyrrole functionalized extended molecular systems and applications for environmental concerns. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/61816

Chicago Manual of Style (16th Edition):

Lee, Juhoon. “Syntheses of calix[4]pyrrole functionalized extended molecular systems and applications for environmental concerns.” 2017. Doctoral Dissertation, University of Texas – Austin. Accessed September 23, 2019. http://hdl.handle.net/2152/61816.

MLA Handbook (7th Edition):

Lee, Juhoon. “Syntheses of calix[4]pyrrole functionalized extended molecular systems and applications for environmental concerns.” 2017. Web. 23 Sep 2019.

Vancouver:

Lee J. Syntheses of calix[4]pyrrole functionalized extended molecular systems and applications for environmental concerns. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2017. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/2152/61816.

Council of Science Editors:

Lee J. Syntheses of calix[4]pyrrole functionalized extended molecular systems and applications for environmental concerns. [Doctoral Dissertation]. University of Texas – Austin; 2017. Available from: http://hdl.handle.net/2152/61816


University of Texas – Austin

26. -9265-9181. Characterization of two radical S-adenosyl-L-methionine enzymes in the biosynthesis of aminoglycosides.

Degree: PhD, Chemistry, 2016, University of Texas – Austin

 Biosynthetic studies of natural products are essential to the discovery and development of new drugs, because by understanding biosynthetic pathways and the enzymes that characterize… (more)

Subjects/Keywords: Biosynthesis; Aminoglycoside; Radical SAM; Enzyme

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APA (6th Edition):

-9265-9181. (2016). Characterization of two radical S-adenosyl-L-methionine enzymes in the biosynthesis of aminoglycosides. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/68375

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Chicago Manual of Style (16th Edition):

-9265-9181. “Characterization of two radical S-adenosyl-L-methionine enzymes in the biosynthesis of aminoglycosides.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed September 23, 2019. http://hdl.handle.net/2152/68375.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

-9265-9181. “Characterization of two radical S-adenosyl-L-methionine enzymes in the biosynthesis of aminoglycosides.” 2016. Web. 23 Sep 2019.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

-9265-9181. Characterization of two radical S-adenosyl-L-methionine enzymes in the biosynthesis of aminoglycosides. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/2152/68375.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

-9265-9181. Characterization of two radical S-adenosyl-L-methionine enzymes in the biosynthesis of aminoglycosides. [Doctoral Dissertation]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/68375

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Author name may be incomplete


University of Texas – Austin

27. -6179-7645. Transition metal catalyzed C-C bond formation via transfer hydrogenation : from methodology development to polycyclic aromatic hydrocarbon syntheses.

Degree: PhD, Chemistry, 2019, University of Texas – Austin

 Since the Nobel prize-winning discovery of the Diels-Alder reaction in 1928, cycloaddition reactions—chemical transformations to construct ubiquitous cyclic organic molecules—are one of the most important… (more)

Subjects/Keywords: Transition metal; C-C bond forming reactions; Cycloadditions; Hydrogen transfer; Polycyclic aromatic hydrocarbons; Organometallics

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APA (6th Edition):

-6179-7645. (2019). Transition metal catalyzed C-C bond formation via transfer hydrogenation : from methodology development to polycyclic aromatic hydrocarbon syntheses. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/2170

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-6179-7645. “Transition metal catalyzed C-C bond formation via transfer hydrogenation : from methodology development to polycyclic aromatic hydrocarbon syntheses.” 2019. Doctoral Dissertation, University of Texas – Austin. Accessed September 23, 2019. http://dx.doi.org/10.26153/tsw/2170.

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Author name may be incomplete

MLA Handbook (7th Edition):

-6179-7645. “Transition metal catalyzed C-C bond formation via transfer hydrogenation : from methodology development to polycyclic aromatic hydrocarbon syntheses.” 2019. Web. 23 Sep 2019.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

-6179-7645. Transition metal catalyzed C-C bond formation via transfer hydrogenation : from methodology development to polycyclic aromatic hydrocarbon syntheses. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2019. [cited 2019 Sep 23]. Available from: http://dx.doi.org/10.26153/tsw/2170.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

-6179-7645. Transition metal catalyzed C-C bond formation via transfer hydrogenation : from methodology development to polycyclic aromatic hydrocarbon syntheses. [Doctoral Dissertation]. University of Texas – Austin; 2019. Available from: http://dx.doi.org/10.26153/tsw/2170

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Author name may be incomplete


University of Texas – Austin

28. -1756-2037. Total synthesis and chemical modification of small molecules: a study of axonal regeneration and aryl oxidation.

Degree: PhD, Chemistry, 2015, University of Texas – Austin

 Injuries to the central nervous system are irreversible and debilitating due to the limited regrowth of damaged or severed neurons. Two small molecules, xanthofulvin and… (more)

Subjects/Keywords: Total synthesis; Vinaxanthone; Xanthofulvin; Regeneration; Phthaloyl peroxide

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APA (6th Edition):

-1756-2037. (2015). Total synthesis and chemical modification of small molecules: a study of axonal regeneration and aryl oxidation. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/30463

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-1756-2037. “Total synthesis and chemical modification of small molecules: a study of axonal regeneration and aryl oxidation.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed September 23, 2019. http://hdl.handle.net/2152/30463.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

-1756-2037. “Total synthesis and chemical modification of small molecules: a study of axonal regeneration and aryl oxidation.” 2015. Web. 23 Sep 2019.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

-1756-2037. Total synthesis and chemical modification of small molecules: a study of axonal regeneration and aryl oxidation. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/2152/30463.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

-1756-2037. Total synthesis and chemical modification of small molecules: a study of axonal regeneration and aryl oxidation. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/30463

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete


University of Texas – Austin

29. Feng, Jiajie. Catalytic diastereo- and enantioselective formation of all-carbon quaternary centers: ir-catalyzed tert-(hydroxy)prenylation of alcohols and its application to modular syntheses of terpenoids.

Degree: PhD, Chemistry, 2017, University of Texas – Austin

 All-carbon quaternary stereocenters are ubiquitous in bioactive natural products as well as pharmaceutical molecules. However, stereoselective access of these structural motifs is still a challenge… (more)

Subjects/Keywords: Quaternary stereocenters; Iridium catalysis; Terpenoid natural products; Modular total synthesis

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APA (6th Edition):

Feng, J. (2017). Catalytic diastereo- and enantioselective formation of all-carbon quaternary centers: ir-catalyzed tert-(hydroxy)prenylation of alcohols and its application to modular syntheses of terpenoids. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/47159

Chicago Manual of Style (16th Edition):

Feng, Jiajie. “Catalytic diastereo- and enantioselective formation of all-carbon quaternary centers: ir-catalyzed tert-(hydroxy)prenylation of alcohols and its application to modular syntheses of terpenoids.” 2017. Doctoral Dissertation, University of Texas – Austin. Accessed September 23, 2019. http://hdl.handle.net/2152/47159.

MLA Handbook (7th Edition):

Feng, Jiajie. “Catalytic diastereo- and enantioselective formation of all-carbon quaternary centers: ir-catalyzed tert-(hydroxy)prenylation of alcohols and its application to modular syntheses of terpenoids.” 2017. Web. 23 Sep 2019.

Vancouver:

Feng J. Catalytic diastereo- and enantioselective formation of all-carbon quaternary centers: ir-catalyzed tert-(hydroxy)prenylation of alcohols and its application to modular syntheses of terpenoids. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2017. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/2152/47159.

Council of Science Editors:

Feng J. Catalytic diastereo- and enantioselective formation of all-carbon quaternary centers: ir-catalyzed tert-(hydroxy)prenylation of alcohols and its application to modular syntheses of terpenoids. [Doctoral Dissertation]. University of Texas – Austin; 2017. Available from: http://hdl.handle.net/2152/47159


University of Texas – Austin

30. Liu, Cheng-Hao. Probing chemical mechanism of two enzyme-catalyzed reactions by chiral substrate analogues.

Degree: PhD, Chemistry, 2014, University of Texas – Austin

 Enzymes are biological catalysts which greatly accelerate the rate of chemical reactions with remarkable substrate specificity and stereoselectivity. To optimize their catalytic abilities, many enzymes… (more)

Subjects/Keywords: Enzyme mechanism; Chiral substrate; ACC deaminase; PLP; Difluorocyclopropane; Tight-binding inhibitor; IspH; chiral methyl analysis; Iron-sulfur cluster

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

APA (6th Edition):

Liu, C. (2014). Probing chemical mechanism of two enzyme-catalyzed reactions by chiral substrate analogues. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/63859

Chicago Manual of Style (16th Edition):

Liu, Cheng-Hao. “Probing chemical mechanism of two enzyme-catalyzed reactions by chiral substrate analogues.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed September 23, 2019. http://hdl.handle.net/2152/63859.

MLA Handbook (7th Edition):

Liu, Cheng-Hao. “Probing chemical mechanism of two enzyme-catalyzed reactions by chiral substrate analogues.” 2014. Web. 23 Sep 2019.

Vancouver:

Liu C. Probing chemical mechanism of two enzyme-catalyzed reactions by chiral substrate analogues. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/2152/63859.

Council of Science Editors:

Liu C. Probing chemical mechanism of two enzyme-catalyzed reactions by chiral substrate analogues. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/63859

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