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You searched for +publisher:"University of Texas – Austin" +contributor:("Kerwin, Sean M"). Showing records 1 – 16 of 16 total matches.

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1. Gilbreath, Bradford Lynd. Synthetic utility and reactivity of N-alkynylazoles.

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

 The chemistry of N-alkynylazoles is a newly emerging area of chemistry with particular interest in heterocycle synthesis. Synthetic preparations of this class of molecule have… (more)

Subjects/Keywords: N-alkynylazoles

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APA (6th Edition):

Gilbreath, B. L. (2014). Synthetic utility and reactivity of N-alkynylazoles. (Masters Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/28741

Chicago Manual of Style (16th Edition):

Gilbreath, Bradford Lynd. “Synthetic utility and reactivity of N-alkynylazoles.” 2014. Masters Thesis, University of Texas – Austin. Accessed February 24, 2020. http://hdl.handle.net/2152/28741.

MLA Handbook (7th Edition):

Gilbreath, Bradford Lynd. “Synthetic utility and reactivity of N-alkynylazoles.” 2014. Web. 24 Feb 2020.

Vancouver:

Gilbreath BL. Synthetic utility and reactivity of N-alkynylazoles. [Internet] [Masters thesis]. University of Texas – Austin; 2014. [cited 2020 Feb 24]. Available from: http://hdl.handle.net/2152/28741.

Council of Science Editors:

Gilbreath BL. Synthetic utility and reactivity of N-alkynylazoles. [Masters Thesis]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/28741


University of Texas – Austin

2. 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 February 24, 2020. 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. 24 Feb 2020.

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 2020 Feb 24]. 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

3. Ikkanda, Brian Aki. Assembly of complimentary naphthyl units in nucleotidomimetic foldamers.

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

 The large and complex architectures found in biomolecules not only are an amazing feat of molecular construction, but they also function to carry out all… (more)

Subjects/Keywords: Aromatic; DNA; Deoxyribonucleic acid; DAN; NDI; Foldamer; Organic chemistry; Bioorganic chemistry; Chemical biology

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APA (6th Edition):

Ikkanda, B. A. (2016). Assembly of complimentary naphthyl units in nucleotidomimetic foldamers. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/68382

Chicago Manual of Style (16th Edition):

Ikkanda, Brian Aki. “Assembly of complimentary naphthyl units in nucleotidomimetic foldamers.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed February 24, 2020. http://hdl.handle.net/2152/68382.

MLA Handbook (7th Edition):

Ikkanda, Brian Aki. “Assembly of complimentary naphthyl units in nucleotidomimetic foldamers.” 2016. Web. 24 Feb 2020.

Vancouver:

Ikkanda BA. Assembly of complimentary naphthyl units in nucleotidomimetic foldamers. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2020 Feb 24]. Available from: http://hdl.handle.net/2152/68382.

Council of Science Editors:

Ikkanda BA. Assembly of complimentary naphthyl units in nucleotidomimetic foldamers. [Doctoral Dissertation]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/68382


University of Texas – Austin

4. Reinus, Brandon Joseph. N-alkynylations of substituted pyrroles with 1-bromo-1-alkynes and C-alkylations and C-alkenylations of cyclic 1,2-diketones.

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

 Nitrogen-substituted alkynes are a unique class of compounds that have found general use in organic synthesis. The catalytic synthesis of N-substituted alkynes offers a rapid… (more)

Subjects/Keywords: N-alkynyl pyrrole; Copper; Rhodium

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APA (6th Edition):

Reinus, B. J. (2019). N-alkynylations of substituted pyrroles with 1-bromo-1-alkynes and C-alkylations and C-alkenylations of cyclic 1,2-diketones. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/2974

Chicago Manual of Style (16th Edition):

Reinus, Brandon Joseph. “N-alkynylations of substituted pyrroles with 1-bromo-1-alkynes and C-alkylations and C-alkenylations of cyclic 1,2-diketones.” 2019. Doctoral Dissertation, University of Texas – Austin. Accessed February 24, 2020. http://dx.doi.org/10.26153/tsw/2974.

MLA Handbook (7th Edition):

Reinus, Brandon Joseph. “N-alkynylations of substituted pyrroles with 1-bromo-1-alkynes and C-alkylations and C-alkenylations of cyclic 1,2-diketones.” 2019. Web. 24 Feb 2020.

Vancouver:

Reinus BJ. N-alkynylations of substituted pyrroles with 1-bromo-1-alkynes and C-alkylations and C-alkenylations of cyclic 1,2-diketones. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2019. [cited 2020 Feb 24]. Available from: http://dx.doi.org/10.26153/tsw/2974.

Council of Science Editors:

Reinus BJ. N-alkynylations of substituted pyrroles with 1-bromo-1-alkynes and C-alkylations and C-alkenylations of cyclic 1,2-diketones. [Doctoral Dissertation]. University of Texas – Austin; 2019. Available from: http://dx.doi.org/10.26153/tsw/2974

5. Diehl, Katharine Louise. Development of cross-reactive receptors based on serum albumin.

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

 In recent years, differential sensing has become an increasingly popular approach to molecular recognition. Mimicking the mammalian senses of taste and smell, arrays of semi-selective… (more)

Subjects/Keywords: Array sensing; Chemometrics; Glyceride; Squaraine; Conjugate acceptor; Serum albumin

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APA (6th Edition):

Diehl, K. L. (2015). Development of cross-reactive receptors based on serum albumin. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/46543

Chicago Manual of Style (16th Edition):

Diehl, Katharine Louise. “Development of cross-reactive receptors based on serum albumin.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed February 24, 2020. http://hdl.handle.net/2152/46543.

MLA Handbook (7th Edition):

Diehl, Katharine Louise. “Development of cross-reactive receptors based on serum albumin.” 2015. Web. 24 Feb 2020.

Vancouver:

Diehl KL. Development of cross-reactive receptors based on serum albumin. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2020 Feb 24]. Available from: http://hdl.handle.net/2152/46543.

Council of Science Editors:

Diehl KL. Development of cross-reactive receptors based on serum albumin. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/46543


University of Texas – Austin

6. -7992-3267. Structure-based mechanism of hydratase-aldolases in the Type I aldolase superfamily and structures of tautomerase superfamily members.

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

 Polycyclic Aromatic Hydrocarbons (PAHs) are composed of multiple benzene-like rings and their bacterial catabolism has potential utility for bioremediation. In the breakdown of each ring,… (more)

Subjects/Keywords: Hydratase-aldolase; Naphthalene; Phenanthrene; Mycobacterium vanbaalenii PYR-1; Pseudomonas putida G7; Type I aldolase; 4-oxalocrotonate tautomerase; Cis-3-chloroacrylic acid dehalogenase; Malonate semialdehyde decarboxylase; Tautomerase superfamily

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APA (6th Edition):

-7992-3267. (2017). Structure-based mechanism of hydratase-aldolases in the Type I aldolase superfamily and structures of tautomerase superfamily members. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/2230

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-7992-3267. “Structure-based mechanism of hydratase-aldolases in the Type I aldolase superfamily and structures of tautomerase superfamily members.” 2017. Doctoral Dissertation, University of Texas – Austin. Accessed February 24, 2020. http://dx.doi.org/10.26153/tsw/2230.

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Author name may be incomplete

MLA Handbook (7th Edition):

-7992-3267. “Structure-based mechanism of hydratase-aldolases in the Type I aldolase superfamily and structures of tautomerase superfamily members.” 2017. Web. 24 Feb 2020.

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

Vancouver:

-7992-3267. Structure-based mechanism of hydratase-aldolases in the Type I aldolase superfamily and structures of tautomerase superfamily members. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2017. [cited 2020 Feb 24]. Available from: http://dx.doi.org/10.26153/tsw/2230.

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

Council of Science Editors:

-7992-3267. Structure-based mechanism of hydratase-aldolases in the Type I aldolase superfamily and structures of tautomerase superfamily members. [Doctoral Dissertation]. University of Texas – Austin; 2017. Available from: http://dx.doi.org/10.26153/tsw/2230

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Author name may be incomplete


University of Texas – Austin

7. -5840-9966. Calix[4]pyrrole-based molecular self-assembly.

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

 Over the last two decades, calix[4]pyrroles – teterapyrrolic macrocycle linked through α or meso-like positions by sp³-hybridized carbon atoms – have been exploited as strong… (more)

Subjects/Keywords: Self-assembly; Calix[4]pyrrole; Supramolecular polymer; Molecular capsule; Multiple equilibrium

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APA (6th Edition):

-5840-9966. (2015). Calix[4]pyrrole-based molecular self-assembly. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/46715

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-5840-9966. “Calix[4]pyrrole-based molecular self-assembly.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed February 24, 2020. http://hdl.handle.net/2152/46715.

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

MLA Handbook (7th Edition):

-5840-9966. “Calix[4]pyrrole-based molecular self-assembly.” 2015. Web. 24 Feb 2020.

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

Vancouver:

-5840-9966. Calix[4]pyrrole-based molecular self-assembly. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2020 Feb 24]. Available from: http://hdl.handle.net/2152/46715.

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

Council of Science Editors:

-5840-9966. Calix[4]pyrrole-based molecular self-assembly. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/46715

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


University of Texas – Austin

8. Romo, Anthony James. Discovery of the amipurimycin and miharamycins biosynthetic gene clusters and insight into the biosynthesis of nogalamycin.

Degree: PhD, Pharmaceutical Sciences, 2019, University of Texas – Austin

 Advancements in our ability to obtain high quality bacterial whole genome sequences have increased the rate natural product biosynthetic gene clusters are identified, but these… (more)

Subjects/Keywords: Next generation sequencing; Peptidyl nucleoside antibiotics; Gene cluster; Streptomyces

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APA (6th Edition):

Romo, A. J. (2019). Discovery of the amipurimycin and miharamycins biosynthetic gene clusters and insight into the biosynthesis of nogalamycin. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/2198

Chicago Manual of Style (16th Edition):

Romo, Anthony James. “Discovery of the amipurimycin and miharamycins biosynthetic gene clusters and insight into the biosynthesis of nogalamycin.” 2019. Doctoral Dissertation, University of Texas – Austin. Accessed February 24, 2020. http://dx.doi.org/10.26153/tsw/2198.

MLA Handbook (7th Edition):

Romo, Anthony James. “Discovery of the amipurimycin and miharamycins biosynthetic gene clusters and insight into the biosynthesis of nogalamycin.” 2019. Web. 24 Feb 2020.

Vancouver:

Romo AJ. Discovery of the amipurimycin and miharamycins biosynthetic gene clusters and insight into the biosynthesis of nogalamycin. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2019. [cited 2020 Feb 24]. Available from: http://dx.doi.org/10.26153/tsw/2198.

Council of Science Editors:

Romo AJ. Discovery of the amipurimycin and miharamycins biosynthetic gene clusters and insight into the biosynthesis of nogalamycin. [Doctoral Dissertation]. University of Texas – Austin; 2019. Available from: http://dx.doi.org/10.26153/tsw/2198

9. -9681-2721. On the reactions of trans-3-chloroacrylic acid dehalogenase and a cis-3-chloroacrylic acid dehalogenase homologue, Cg10062 : mechanistic and evolutionary implications.

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

 The tautomerase superfamily (TSF) provides an excellent model system to study enzyme specificity, catalysis, and divergent evolution. trans-3-Cholroacrylic acid dehalogenase (CaaD), cis-3-chloroacrylic acid dehalogenase (cis-CaaD),… (more)

Subjects/Keywords: Enzymes; Kinetics; Divergent evolution

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APA (6th Edition):

-9681-2721. (2015). On the reactions of trans-3-chloroacrylic acid dehalogenase and a cis-3-chloroacrylic acid dehalogenase homologue, Cg10062 : mechanistic and evolutionary implications. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/30531

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-9681-2721. “On the reactions of trans-3-chloroacrylic acid dehalogenase and a cis-3-chloroacrylic acid dehalogenase homologue, Cg10062 : mechanistic and evolutionary implications.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed February 24, 2020. http://hdl.handle.net/2152/30531.

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

MLA Handbook (7th Edition):

-9681-2721. “On the reactions of trans-3-chloroacrylic acid dehalogenase and a cis-3-chloroacrylic acid dehalogenase homologue, Cg10062 : mechanistic and evolutionary implications.” 2015. Web. 24 Feb 2020.

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

Vancouver:

-9681-2721. On the reactions of trans-3-chloroacrylic acid dehalogenase and a cis-3-chloroacrylic acid dehalogenase homologue, Cg10062 : mechanistic and evolutionary implications. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2020 Feb 24]. Available from: http://hdl.handle.net/2152/30531.

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

Council of Science Editors:

-9681-2721. On the reactions of trans-3-chloroacrylic acid dehalogenase and a cis-3-chloroacrylic acid dehalogenase homologue, Cg10062 : mechanistic and evolutionary implications. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/30531

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


University of Texas – Austin

10. Kern, Jonathan Thurston. Studies on 3,4,9,10-perylenetetracarboxylic acid diimide based ligands as G-quadruplex DNA interactive agents.

Degree: PhD, Ecology, Evolution, and Behavior, 2002, University of Texas – Austin

 G-quadruplex DNA is a diverse family of structures found at the ends of eukaryotic telomeres that have been implicated in several biological processes, including telomere… (more)

Subjects/Keywords: Nucleic acids – Synthesis; DNA-ligand interactions

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APA (6th Edition):

Kern, J. T. (2002). Studies on 3,4,9,10-perylenetetracarboxylic acid diimide based ligands as G-quadruplex DNA interactive agents. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/693

Chicago Manual of Style (16th Edition):

Kern, Jonathan Thurston. “Studies on 3,4,9,10-perylenetetracarboxylic acid diimide based ligands as G-quadruplex DNA interactive agents.” 2002. Doctoral Dissertation, University of Texas – Austin. Accessed February 24, 2020. http://hdl.handle.net/2152/693.

MLA Handbook (7th Edition):

Kern, Jonathan Thurston. “Studies on 3,4,9,10-perylenetetracarboxylic acid diimide based ligands as G-quadruplex DNA interactive agents.” 2002. Web. 24 Feb 2020.

Vancouver:

Kern JT. Studies on 3,4,9,10-perylenetetracarboxylic acid diimide based ligands as G-quadruplex DNA interactive agents. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2002. [cited 2020 Feb 24]. Available from: http://hdl.handle.net/2152/693.

Council of Science Editors:

Kern JT. Studies on 3,4,9,10-perylenetetracarboxylic acid diimide based ligands as G-quadruplex DNA interactive agents. [Doctoral Dissertation]. University of Texas – Austin; 2002. Available from: http://hdl.handle.net/2152/693

11. Jewett, Ivan Tucker. Development of iminium ion cascade methodologies and their application to the synthesis of complex molecules.

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

 In the interests of synthetic efficiency several cascade reactions involving iminium ion intermediates have developed to allow for the rapid assembly of complex molecules from… (more)

Subjects/Keywords: Iminium ion; Cascade reactions; Quinolizidine; Alkaloid; Actinophyllic acid

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APA (6th Edition):

Jewett, I. T. (2010). Development of iminium ion cascade methodologies and their application to the synthesis of complex molecules. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/30932

Chicago Manual of Style (16th Edition):

Jewett, Ivan Tucker. “Development of iminium ion cascade methodologies and their application to the synthesis of complex molecules.” 2010. Doctoral Dissertation, University of Texas – Austin. Accessed February 24, 2020. http://hdl.handle.net/2152/30932.

MLA Handbook (7th Edition):

Jewett, Ivan Tucker. “Development of iminium ion cascade methodologies and their application to the synthesis of complex molecules.” 2010. Web. 24 Feb 2020.

Vancouver:

Jewett IT. Development of iminium ion cascade methodologies and their application to the synthesis of complex molecules. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2010. [cited 2020 Feb 24]. Available from: http://hdl.handle.net/2152/30932.

Council of Science Editors:

Jewett IT. Development of iminium ion cascade methodologies and their application to the synthesis of complex molecules. [Doctoral Dissertation]. University of Texas – Austin; 2010. Available from: http://hdl.handle.net/2152/30932

12. -5628-4490. Transition metal catalyzed regioselective carbon-carbon bond formation mediated by transfer hydrogenation.

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

 One of the more formidable challenges in the synthesis of complex organic molecules remains the efficient formation of carbon-carbon bonds. The development of a broad… (more)

Subjects/Keywords: Homogenous catalysis; C-C couplings; Ruthenium; Nickel

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APA (6th Edition):

-5628-4490. (2015). Transition metal catalyzed regioselective carbon-carbon bond formation mediated by transfer hydrogenation. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/30512

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-5628-4490. “Transition metal catalyzed regioselective carbon-carbon bond formation mediated by transfer hydrogenation.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed February 24, 2020. http://hdl.handle.net/2152/30512.

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Author name may be incomplete

MLA Handbook (7th Edition):

-5628-4490. “Transition metal catalyzed regioselective carbon-carbon bond formation mediated by transfer hydrogenation.” 2015. Web. 24 Feb 2020.

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

Vancouver:

-5628-4490. Transition metal catalyzed regioselective carbon-carbon bond formation mediated by transfer hydrogenation. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2020 Feb 24]. Available from: http://hdl.handle.net/2152/30512.

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

Council of Science Editors:

-5628-4490. Transition metal catalyzed regioselective carbon-carbon bond formation mediated by transfer hydrogenation. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/30512

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Author name may be incomplete

13. -1450-5221. A systems pharmacology approach to discovery of drugs to ameliorate oxidant stress in human endothelial cells.

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

 Ischemia is characterized by reduced blood flow to an area of the body which can then cause cellular injury through the generation of reactive oxygen… (more)

Subjects/Keywords: Oxidant Stress; Ischemia; Reperfusion; Microarray; Systems Pharmacology; Systems Biology; CDDO

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APA (6th Edition):

-1450-5221. (2015). A systems pharmacology approach to discovery of drugs to ameliorate oxidant stress in human endothelial cells. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/31019

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Chicago Manual of Style (16th Edition):

-1450-5221. “A systems pharmacology approach to discovery of drugs to ameliorate oxidant stress in human endothelial cells.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed February 24, 2020. http://hdl.handle.net/2152/31019.

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Author name may be incomplete

MLA Handbook (7th Edition):

-1450-5221. “A systems pharmacology approach to discovery of drugs to ameliorate oxidant stress in human endothelial cells.” 2015. Web. 24 Feb 2020.

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

Vancouver:

-1450-5221. A systems pharmacology approach to discovery of drugs to ameliorate oxidant stress in human endothelial cells. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2020 Feb 24]. Available from: http://hdl.handle.net/2152/31019.

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

Council of Science Editors:

-1450-5221. A systems pharmacology approach to discovery of drugs to ameliorate oxidant stress in human endothelial cells. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/31019

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14. Brough, Chris Eugene. Novel uses of pharmaceutical polymers as enabled by KinetiSol® dispersing.

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

 Poor water-solubility is a common characteristic of drug candidates in pharmaceutical development pipelines today. Various processes have been developed to increase the solubility, dissolution rate… (more)

Subjects/Keywords: KinetiSol Dispersing; KinetiSol® Dispersing; Polyvinyl alcohol; PVAL; Amorphous dispersion; Amorphous solid dispersions; Pharmaceutical development; Nano-crystal delivery; Poorly water-soluble drugs; Itraconazole; ITZ; Concentration enhancing polymers; Abuse deterrant delivery; Abuse deterrant formulations; Molecular weight; Drug and polymer interaction

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APA (6th Edition):

Brough, C. E. (2015). Novel uses of pharmaceutical polymers as enabled by KinetiSol® dispersing. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/46899

Chicago Manual of Style (16th Edition):

Brough, Chris Eugene. “Novel uses of pharmaceutical polymers as enabled by KinetiSol® dispersing.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed February 24, 2020. http://hdl.handle.net/2152/46899.

MLA Handbook (7th Edition):

Brough, Chris Eugene. “Novel uses of pharmaceutical polymers as enabled by KinetiSol® dispersing.” 2015. Web. 24 Feb 2020.

Vancouver:

Brough CE. Novel uses of pharmaceutical polymers as enabled by KinetiSol® dispersing. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2020 Feb 24]. Available from: http://hdl.handle.net/2152/46899.

Council of Science Editors:

Brough CE. Novel uses of pharmaceutical polymers as enabled by KinetiSol® dispersing. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/46899

15. Seipp, Charles Aaron. Guanidinium-based receptors for anion separations.

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

 Herein, work on guanidinium-based anion receptors and their anion separation properties are described. First, a novel receptor based on the N,N’-bis(2-pyridyl)guanidinium motif is rationally designed,… (more)

Subjects/Keywords: Molecular recognition; Anions; Guanidiniums

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

APA (6th Edition):

Seipp, C. A. (2018). Guanidinium-based receptors for anion separations. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/63302

Chicago Manual of Style (16th Edition):

Seipp, Charles Aaron. “Guanidinium-based receptors for anion separations.” 2018. Doctoral Dissertation, University of Texas – Austin. Accessed February 24, 2020. http://hdl.handle.net/2152/63302.

MLA Handbook (7th Edition):

Seipp, Charles Aaron. “Guanidinium-based receptors for anion separations.” 2018. Web. 24 Feb 2020.

Vancouver:

Seipp CA. Guanidinium-based receptors for anion separations. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2018. [cited 2020 Feb 24]. Available from: http://hdl.handle.net/2152/63302.

Council of Science Editors:

Seipp CA. Guanidinium-based receptors for anion separations. [Doctoral Dissertation]. University of Texas – Austin; 2018. Available from: http://hdl.handle.net/2152/63302

16. -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

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

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

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 February 24, 2020. 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. 24 Feb 2020.

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 2020 Feb 24]. 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

.