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You searched for +publisher:"University of Texas – Austin" +contributor:("Keatinge-Clay, Adrian T"). Showing records 1 – 17 of 17 total matches.

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University of Texas – Austin

1. -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

Note: this citation may be lacking information needed for this citation format:
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 October 16, 2019. http://hdl.handle.net/2152/63343.

Note: this citation may be lacking information needed for this citation format:
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. 16 Oct 2019.

Note: this citation may be lacking information needed for this citation format:
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 Oct 16]. Available from: http://hdl.handle.net/2152/63343.

Note: this citation may be lacking information needed for this citation format:
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

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


University of Texas – Austin

2. -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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Author name may be incomplete

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 October 16, 2019. http://hdl.handle.net/2152/65669.

Note: this citation may be lacking information needed for this citation format:
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. 16 Oct 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 Oct 16]. 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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Author name may be incomplete


University of Texas – Austin

3. -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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Author name may be incomplete

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 October 16, 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. 16 Oct 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 Oct 16]. 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

4. -6237-9461. The adenylate cyclase toxin as a target for antibody therapeutics and vaccination against whooping cough.

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

 Whooping cough, also known as pertussis, is caused by the bacterium Bordetella pertussis. Since widespread vaccination with heat-killed whole cell vaccines (wP) in the 1950s,… (more)

Subjects/Keywords: Bordetella pertussis; Whooping cough; Adenylate cyclase toxin; Neutralizing antibodies; Antibody discovery; Vaccine; Epitope; RTX; Receptor binding; Immunodominant

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APA (6th Edition):

-6237-9461. (2015). The adenylate cyclase toxin as a target for antibody therapeutics and vaccination against whooping cough. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/46796

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

Chicago Manual of Style (16th Edition):

-6237-9461. “The adenylate cyclase toxin as a target for antibody therapeutics and vaccination against whooping cough.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed October 16, 2019. http://hdl.handle.net/2152/46796.

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

MLA Handbook (7th Edition):

-6237-9461. “The adenylate cyclase toxin as a target for antibody therapeutics and vaccination against whooping cough.” 2015. Web. 16 Oct 2019.

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

Vancouver:

-6237-9461. The adenylate cyclase toxin as a target for antibody therapeutics and vaccination against whooping cough. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/2152/46796.

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

Council of Science Editors:

-6237-9461. The adenylate cyclase toxin as a target for antibody therapeutics and vaccination against whooping cough. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/46796

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


University of Texas – Austin

5. Garza, Victoria J. Transition metal catalyzed C-C bond formation : advances in carbonyl addition.

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

 Transition metal catalyzed transfer hydrogenative methods for carbon-carbon bond construction are attractive alternatives to tradition carbonyl addition protocols. By generating carbonyl and organometallic species in-situ,… (more)

Subjects/Keywords: Carbonyl addition; Transition metal; Hydrogenative

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APA (6th Edition):

Garza, V. J. (2017). Transition metal catalyzed C-C bond formation : advances in carbonyl addition. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/61903

Chicago Manual of Style (16th Edition):

Garza, Victoria J. “Transition metal catalyzed C-C bond formation : advances in carbonyl addition.” 2017. Doctoral Dissertation, University of Texas – Austin. Accessed October 16, 2019. http://hdl.handle.net/2152/61903.

MLA Handbook (7th Edition):

Garza, Victoria J. “Transition metal catalyzed C-C bond formation : advances in carbonyl addition.” 2017. Web. 16 Oct 2019.

Vancouver:

Garza VJ. Transition metal catalyzed C-C bond formation : advances in carbonyl addition. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2017. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/2152/61903.

Council of Science Editors:

Garza VJ. Transition metal catalyzed C-C bond formation : advances in carbonyl addition. [Doctoral Dissertation]. University of Texas – Austin; 2017. Available from: http://hdl.handle.net/2152/61903


University of Texas – Austin

6. 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 October 16, 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. 16 Oct 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 Oct 16]. 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

7. 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 October 16, 2019. 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. 16 Oct 2019.

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 2019 Oct 16]. 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


University of Texas – Austin

8. Lamech, Lilian Tawsein M. Mitochondrial tyrosyl-tRNA synthetases : evolving a function beyond translation.

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

 Pezizomycotina mitochondrial tyrosyl-tRNA synthetases (mtTyrRS) are bifunctional, with the ability to splice group I introns in addition to catalyzing aminoacylation. Work done with the Neurospora… (more)

Subjects/Keywords: TRNA; Tyrosyl-tRNA synthetase; CYT-18; MtTyrRS; SAXS; X-ray crystallography

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APA (6th Edition):

Lamech, L. T. M. (2014). Mitochondrial tyrosyl-tRNA synthetases : evolving a function beyond translation. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/31554

Chicago Manual of Style (16th Edition):

Lamech, Lilian Tawsein M. “Mitochondrial tyrosyl-tRNA synthetases : evolving a function beyond translation.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed October 16, 2019. http://hdl.handle.net/2152/31554.

MLA Handbook (7th Edition):

Lamech, Lilian Tawsein M. “Mitochondrial tyrosyl-tRNA synthetases : evolving a function beyond translation.” 2014. Web. 16 Oct 2019.

Vancouver:

Lamech LTM. Mitochondrial tyrosyl-tRNA synthetases : evolving a function beyond translation. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/2152/31554.

Council of Science Editors:

Lamech LTM. Mitochondrial tyrosyl-tRNA synthetases : evolving a function beyond translation. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/31554


University of Texas – Austin

9. 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 October 16, 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. 16 Oct 2019.

Vancouver:

Lin C. Biosynthetic studies of lincomycin A, a thiosugar-containing natural product. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2019. [cited 2019 Oct 16]. 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

10. 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 October 16, 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. 16 Oct 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 Oct 16]. 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

11. 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 October 16, 2019. http://hdl.handle.net/2152/68382.

MLA Handbook (7th Edition):

Ikkanda, Brian Aki. “Assembly of complimentary naphthyl units in nucleotidomimetic foldamers.” 2016. Web. 16 Oct 2019.

Vancouver:

Ikkanda BA. Assembly of complimentary naphthyl units in nucleotidomimetic foldamers. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2019 Oct 16]. 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

12. Brantley, Johnathan Nathanael. Mechanical activations of synthetic and biological systems.

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

 Polymer mechanochemistry, wherein exogenous forces are harnessed to drive chemical processes within polymeric matrices, has afforded access to an astounding array of otherwise kinetically prohibitive… (more)

Subjects/Keywords: Polymer Mechanochemistry; Triazole Cycloreversion; Suppressed Reactivity; Biomechanophores

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APA (6th Edition):

Brantley, J. N. (2014). Mechanical activations of synthetic and biological systems. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/31307

Chicago Manual of Style (16th Edition):

Brantley, Johnathan Nathanael. “Mechanical activations of synthetic and biological systems.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed October 16, 2019. http://hdl.handle.net/2152/31307.

MLA Handbook (7th Edition):

Brantley, Johnathan Nathanael. “Mechanical activations of synthetic and biological systems.” 2014. Web. 16 Oct 2019.

Vancouver:

Brantley JN. Mechanical activations of synthetic and biological systems. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/2152/31307.

Council of Science Editors:

Brantley JN. Mechanical activations of synthetic and biological systems. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/31307

13. Axelrod, Abram Joseph. Total syntheses of the neuroregenerative natural products vinaxanthone and xanthofulvin and biosynthetic studies.

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

 Total syntheses of the neuroregenerative natural products vinaxanthone and xanthofulvin have been accomplished. The synthetic routes to both molecules utilize a highly regioselective furan Diels-Alder… (more)

Subjects/Keywords: Natural products; Total synthesis; Neuroregeneration; Polyketide; Xanthone; Chromone

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APA (6th Edition):

Axelrod, A. J. (2012). Total syntheses of the neuroregenerative natural products vinaxanthone and xanthofulvin and biosynthetic studies. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/30392

Chicago Manual of Style (16th Edition):

Axelrod, Abram Joseph. “Total syntheses of the neuroregenerative natural products vinaxanthone and xanthofulvin and biosynthetic studies.” 2012. Doctoral Dissertation, University of Texas – Austin. Accessed October 16, 2019. http://hdl.handle.net/2152/30392.

MLA Handbook (7th Edition):

Axelrod, Abram Joseph. “Total syntheses of the neuroregenerative natural products vinaxanthone and xanthofulvin and biosynthetic studies.” 2012. Web. 16 Oct 2019.

Vancouver:

Axelrod AJ. Total syntheses of the neuroregenerative natural products vinaxanthone and xanthofulvin and biosynthetic studies. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2012. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/2152/30392.

Council of Science Editors:

Axelrod AJ. Total syntheses of the neuroregenerative natural products vinaxanthone and xanthofulvin and biosynthetic studies. [Doctoral Dissertation]. University of Texas – Austin; 2012. Available from: http://hdl.handle.net/2152/30392


University of Texas – Austin

14. -8470-1458. Enantiomeric excess determination using circular dichroism spectroscopy and studies of reversible covalent reactions: Enantiomeric excess determination using circular dichroism spectroscopy: Studies of reversible covalent reactions: Study of four orthogonal, reversible covalent reactions.

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

 The unifying topic of this thesis is that of supramolecular and reversible covalent chemistry. Both supramolecular and reversible covalent reactions operate under thermodynamic control, leading… (more)

Subjects/Keywords: Enantiomeric excess; Stereochemistry; Circular dichroism; Supramolecular chemistry; Dynamic combinatorial chemistry; Dynamic covalent reactions

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APA (6th Edition):

-8470-1458. (2017). Enantiomeric excess determination using circular dichroism spectroscopy and studies of reversible covalent reactions: Enantiomeric excess determination using circular dichroism spectroscopy: Studies of reversible covalent reactions: Study of four orthogonal, reversible covalent reactions. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/3114

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-8470-1458. “Enantiomeric excess determination using circular dichroism spectroscopy and studies of reversible covalent reactions: Enantiomeric excess determination using circular dichroism spectroscopy: Studies of reversible covalent reactions: Study of four orthogonal, reversible covalent reactions.” 2017. Doctoral Dissertation, University of Texas – Austin. Accessed October 16, 2019. http://dx.doi.org/10.26153/tsw/3114.

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Author name may be incomplete

MLA Handbook (7th Edition):

-8470-1458. “Enantiomeric excess determination using circular dichroism spectroscopy and studies of reversible covalent reactions: Enantiomeric excess determination using circular dichroism spectroscopy: Studies of reversible covalent reactions: Study of four orthogonal, reversible covalent reactions.” 2017. Web. 16 Oct 2019.

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

Vancouver:

-8470-1458. Enantiomeric excess determination using circular dichroism spectroscopy and studies of reversible covalent reactions: Enantiomeric excess determination using circular dichroism spectroscopy: Studies of reversible covalent reactions: Study of four orthogonal, reversible covalent reactions. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2017. [cited 2019 Oct 16]. Available from: http://dx.doi.org/10.26153/tsw/3114.

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Author name may be incomplete

Council of Science Editors:

-8470-1458. Enantiomeric excess determination using circular dichroism spectroscopy and studies of reversible covalent reactions: Enantiomeric excess determination using circular dichroism spectroscopy: Studies of reversible covalent reactions: Study of four orthogonal, reversible covalent reactions. [Doctoral Dissertation]. University of Texas – Austin; 2017. Available from: http://dx.doi.org/10.26153/tsw/3114

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Author name may be incomplete

15. Meis, Alan Ronald. Synthesis of homoaporphine-type alkaloids via intramolecular phenol alkylation, design and synthesis of a new class of Trypanosoma brucei growth inhibitors, and neurons that matter : using light to tag neuronal ensembles based on function.

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

 The synthesis of a homoaporphine-type alkaloid was accomplished in 10-steps. The synthesis featured a synthetic strategy to establish the key quaternary center through an early… (more)

Subjects/Keywords: Chemistry; Organic chemistry; Synthetic chemistry; Homoaporphine; Trypanosomiasis

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APA (6th Edition):

Meis, A. R. (2017). Synthesis of homoaporphine-type alkaloids via intramolecular phenol alkylation, design and synthesis of a new class of Trypanosoma brucei growth inhibitors, and neurons that matter : using light to tag neuronal ensembles based on function. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/62976

Chicago Manual of Style (16th Edition):

Meis, Alan Ronald. “Synthesis of homoaporphine-type alkaloids via intramolecular phenol alkylation, design and synthesis of a new class of Trypanosoma brucei growth inhibitors, and neurons that matter : using light to tag neuronal ensembles based on function.” 2017. Doctoral Dissertation, University of Texas – Austin. Accessed October 16, 2019. http://hdl.handle.net/2152/62976.

MLA Handbook (7th Edition):

Meis, Alan Ronald. “Synthesis of homoaporphine-type alkaloids via intramolecular phenol alkylation, design and synthesis of a new class of Trypanosoma brucei growth inhibitors, and neurons that matter : using light to tag neuronal ensembles based on function.” 2017. Web. 16 Oct 2019.

Vancouver:

Meis AR. Synthesis of homoaporphine-type alkaloids via intramolecular phenol alkylation, design and synthesis of a new class of Trypanosoma brucei growth inhibitors, and neurons that matter : using light to tag neuronal ensembles based on function. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2017. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/2152/62976.

Council of Science Editors:

Meis AR. Synthesis of homoaporphine-type alkaloids via intramolecular phenol alkylation, design and synthesis of a new class of Trypanosoma brucei growth inhibitors, and neurons that matter : using light to tag neuronal ensembles based on function. [Doctoral Dissertation]. University of Texas – Austin; 2017. Available from: http://hdl.handle.net/2152/62976

16. -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 October 16, 2019. http://hdl.handle.net/2152/30512.

Note: this citation may be lacking information needed for this citation format:
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. 16 Oct 2019.

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 2019 Oct 16]. 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

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

17. Goran, Jacob Michael. The bioelectrochemistry of enzymes and their cofactors at carbon nanotube and nitrogen-doped carbon nanotube electrodes.

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

 This dissertation explores the electrochemical behavior of enzymes and their cofactors at carbon nanotube (CNT) and nitrogen-doped carbon nanotube (N-CNT) electrodes. Two common types of… (more)

Subjects/Keywords: Enzymes; Electrochemistry; Bioelectrochemistry; Cofactors; Carbon nanotubes; Nitrogen-doped carbon nanotubes

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APA (6th Edition):

Goran, J. M. (2014). The bioelectrochemistry of enzymes and their cofactors at carbon nanotube and nitrogen-doped carbon nanotube electrodes. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/30491

Chicago Manual of Style (16th Edition):

Goran, Jacob Michael. “The bioelectrochemistry of enzymes and their cofactors at carbon nanotube and nitrogen-doped carbon nanotube electrodes.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed October 16, 2019. http://hdl.handle.net/2152/30491.

MLA Handbook (7th Edition):

Goran, Jacob Michael. “The bioelectrochemistry of enzymes and their cofactors at carbon nanotube and nitrogen-doped carbon nanotube electrodes.” 2014. Web. 16 Oct 2019.

Vancouver:

Goran JM. The bioelectrochemistry of enzymes and their cofactors at carbon nanotube and nitrogen-doped carbon nanotube electrodes. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/2152/30491.

Council of Science Editors:

Goran JM. The bioelectrochemistry of enzymes and their cofactors at carbon nanotube and nitrogen-doped carbon nanotube electrodes. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/30491

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