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You searched for +publisher:"University of Texas – Austin" +contributor:("Martin, Stephen F"). Showing records 1 – 23 of 23 total matches.

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1. Granger, Brett Adam. Development of multicomponent assembly processes and their application to the synthesis of novel heterocyclic scaffolds and the total synthesis of actinophyllic acid : application of an iminium ion mediated cascade.

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

 Several novel multicomponent assembly processes have been developed for the preparation of a diverse array of complex heterocyclic systems from relatively simple starting materials. These… (more)

Subjects/Keywords: Total synthesis; Natural products; Organic chemistry

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APA (6th Edition):

Granger, B. A. (2013). Development of multicomponent assembly processes and their application to the synthesis of novel heterocyclic scaffolds and the total synthesis of actinophyllic acid : application of an iminium ion mediated cascade. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/26089

Chicago Manual of Style (16th Edition):

Granger, Brett Adam. “Development of multicomponent assembly processes and their application to the synthesis of novel heterocyclic scaffolds and the total synthesis of actinophyllic acid : application of an iminium ion mediated cascade.” 2013. Doctoral Dissertation, University of Texas – Austin. Accessed November 15, 2019. http://hdl.handle.net/2152/26089.

MLA Handbook (7th Edition):

Granger, Brett Adam. “Development of multicomponent assembly processes and their application to the synthesis of novel heterocyclic scaffolds and the total synthesis of actinophyllic acid : application of an iminium ion mediated cascade.” 2013. Web. 15 Nov 2019.

Vancouver:

Granger BA. Development of multicomponent assembly processes and their application to the synthesis of novel heterocyclic scaffolds and the total synthesis of actinophyllic acid : application of an iminium ion mediated cascade. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2013. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/2152/26089.

Council of Science Editors:

Granger BA. Development of multicomponent assembly processes and their application to the synthesis of novel heterocyclic scaffolds and the total synthesis of actinophyllic acid : application of an iminium ion mediated cascade. [Doctoral Dissertation]. University of Texas – Austin; 2013. Available from: http://hdl.handle.net/2152/26089


University of Texas – Austin

2. -8314-1719. Design and synthesis of novel sigma receptor ligands through scaffold minimization and their application towards targeted drug delivery.

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

 Sigma receptors are a class of proteins in which both subtypes (sigma 1 and sigma 2) have been implicated in the pathology of most central… (more)

Subjects/Keywords: Sigma receptors; Sigma receptor ligands; Scaffold minimization; Targeted drug delivery; Ligand-targeted cancer therapeutic

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APA (6th Edition):

-8314-1719. (2019). Design and synthesis of novel sigma receptor ligands through scaffold minimization and their application towards targeted drug delivery. (Masters Thesis). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/2770

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-8314-1719. “Design and synthesis of novel sigma receptor ligands through scaffold minimization and their application towards targeted drug delivery.” 2019. Masters Thesis, University of Texas – Austin. Accessed November 15, 2019. http://dx.doi.org/10.26153/tsw/2770.

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

MLA Handbook (7th Edition):

-8314-1719. “Design and synthesis of novel sigma receptor ligands through scaffold minimization and their application towards targeted drug delivery.” 2019. Web. 15 Nov 2019.

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

Vancouver:

-8314-1719. Design and synthesis of novel sigma receptor ligands through scaffold minimization and their application towards targeted drug delivery. [Internet] [Masters thesis]. University of Texas – Austin; 2019. [cited 2019 Nov 15]. Available from: http://dx.doi.org/10.26153/tsw/2770.

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

Council of Science Editors:

-8314-1719. Design and synthesis of novel sigma receptor ligands through scaffold minimization and their application towards targeted drug delivery. [Masters Thesis]. University of Texas – Austin; 2019. Available from: http://dx.doi.org/10.26153/tsw/2770

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Author name may be incomplete


University of Texas – Austin

3. -3899-8537. Thermodynamic evaluation of torsional strain in peptide backbones : studies on constrained tripeptide Grb2 adaptor protein inhibitors.

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

 A substantial challenge in ligand design for protein-ligand interactions is the accurate prediction of changes in binding energy associated with small structural variations in ligands.… (more)

Subjects/Keywords: Protein-ligand interactions; Preorganization; Peptide synthesis; Isothermal titration calorimetry

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APA (6th Edition):

-3899-8537. (2017). Thermodynamic evaluation of torsional strain in peptide backbones : studies on constrained tripeptide Grb2 adaptor protein inhibitors. (Masters Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/63541

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

Chicago Manual of Style (16th Edition):

-3899-8537. “Thermodynamic evaluation of torsional strain in peptide backbones : studies on constrained tripeptide Grb2 adaptor protein inhibitors.” 2017. Masters Thesis, University of Texas – Austin. Accessed November 15, 2019. http://hdl.handle.net/2152/63541.

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

MLA Handbook (7th Edition):

-3899-8537. “Thermodynamic evaluation of torsional strain in peptide backbones : studies on constrained tripeptide Grb2 adaptor protein inhibitors.” 2017. Web. 15 Nov 2019.

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

Vancouver:

-3899-8537. Thermodynamic evaluation of torsional strain in peptide backbones : studies on constrained tripeptide Grb2 adaptor protein inhibitors. [Internet] [Masters thesis]. University of Texas – Austin; 2017. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/2152/63541.

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

Council of Science Editors:

-3899-8537. Thermodynamic evaluation of torsional strain in peptide backbones : studies on constrained tripeptide Grb2 adaptor protein inhibitors. [Masters Thesis]. University of Texas – Austin; 2017. Available from: http://hdl.handle.net/2152/63541

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


University of Texas – Austin

4. Farley, Christopher Alexander. Design, synthesis, and thermodynamic evaluation of peptidomimetic ligands binding to the Src SH2 domain.

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

 The ability to predict protein-ligand binding affinities is a difficult and elusive goal in the field of molecular recognition. Models exist to predict binding energetics;… (more)

Subjects/Keywords: Protein-ligand interactions; Protein-ligand binding; Ligand preorganization

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APA (6th Edition):

Farley, C. A. (2018). Design, synthesis, and thermodynamic evaluation of peptidomimetic ligands binding to the Src SH2 domain. (Masters Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/68037

Chicago Manual of Style (16th Edition):

Farley, Christopher Alexander. “Design, synthesis, and thermodynamic evaluation of peptidomimetic ligands binding to the Src SH2 domain.” 2018. Masters Thesis, University of Texas – Austin. Accessed November 15, 2019. http://hdl.handle.net/2152/68037.

MLA Handbook (7th Edition):

Farley, Christopher Alexander. “Design, synthesis, and thermodynamic evaluation of peptidomimetic ligands binding to the Src SH2 domain.” 2018. Web. 15 Nov 2019.

Vancouver:

Farley CA. Design, synthesis, and thermodynamic evaluation of peptidomimetic ligands binding to the Src SH2 domain. [Internet] [Masters thesis]. University of Texas – Austin; 2018. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/2152/68037.

Council of Science Editors:

Farley CA. Design, synthesis, and thermodynamic evaluation of peptidomimetic ligands binding to the Src SH2 domain. [Masters Thesis]. University of Texas – Austin; 2018. Available from: http://hdl.handle.net/2152/68037


University of Texas – Austin

5. -7231-5317. Design and synthesis of conformationally constrained ligands for Grb2 SH2 binding and thermodynamic evaluation and the development of a diversity oriented synthesis of 2-arylpiperidines.

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

 The ways in which torsional strain in the bound form of a ligand affects the energetics of protein binding are poorly understood. In order to… (more)

Subjects/Keywords: Protein; Protein-ligand interaction; Diversity oriented synthesis; Iminium ion; Allylsilane; 2-arylpiperidine

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APA (6th Edition):

-7231-5317. (2016). Design and synthesis of conformationally constrained ligands for Grb2 SH2 binding and thermodynamic evaluation and the development of a diversity oriented synthesis of 2-arylpiperidines. (Masters Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/45584

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

Chicago Manual of Style (16th Edition):

-7231-5317. “Design and synthesis of conformationally constrained ligands for Grb2 SH2 binding and thermodynamic evaluation and the development of a diversity oriented synthesis of 2-arylpiperidines.” 2016. Masters Thesis, University of Texas – Austin. Accessed November 15, 2019. http://hdl.handle.net/2152/45584.

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

MLA Handbook (7th Edition):

-7231-5317. “Design and synthesis of conformationally constrained ligands for Grb2 SH2 binding and thermodynamic evaluation and the development of a diversity oriented synthesis of 2-arylpiperidines.” 2016. Web. 15 Nov 2019.

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

Vancouver:

-7231-5317. Design and synthesis of conformationally constrained ligands for Grb2 SH2 binding and thermodynamic evaluation and the development of a diversity oriented synthesis of 2-arylpiperidines. [Internet] [Masters thesis]. University of Texas – Austin; 2016. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/2152/45584.

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

Council of Science Editors:

-7231-5317. Design and synthesis of conformationally constrained ligands for Grb2 SH2 binding and thermodynamic evaluation and the development of a diversity oriented synthesis of 2-arylpiperidines. [Masters Thesis]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/45584

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Author name may be incomplete


University of Texas – Austin

6. Klosowski, Daniel William. Applications of enantioselective halolactonization reactions, synthesis of photocaged compounds for identifying neurons based on function, and progress towards the total synthesis of alstoscholarisine E.

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

 Recently the Martin group developed a bifunctional organic catalyst that promotes highly efficient enantioselective halolactonization reactions for olefinic acids. Using the BINOL-amidine catalyst we invented,… (more)

Subjects/Keywords: Enantioselective halolactonization; Neuron labeling; Total synthesis

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APA (6th Edition):

Klosowski, D. W. (2018). Applications of enantioselective halolactonization reactions, synthesis of photocaged compounds for identifying neurons based on function, and progress towards the total synthesis of alstoscholarisine E. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/68029

Chicago Manual of Style (16th Edition):

Klosowski, Daniel William. “Applications of enantioselective halolactonization reactions, synthesis of photocaged compounds for identifying neurons based on function, and progress towards the total synthesis of alstoscholarisine E.” 2018. Doctoral Dissertation, University of Texas – Austin. Accessed November 15, 2019. http://hdl.handle.net/2152/68029.

MLA Handbook (7th Edition):

Klosowski, Daniel William. “Applications of enantioselective halolactonization reactions, synthesis of photocaged compounds for identifying neurons based on function, and progress towards the total synthesis of alstoscholarisine E.” 2018. Web. 15 Nov 2019.

Vancouver:

Klosowski DW. Applications of enantioselective halolactonization reactions, synthesis of photocaged compounds for identifying neurons based on function, and progress towards the total synthesis of alstoscholarisine E. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2018. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/2152/68029.

Council of Science Editors:

Klosowski DW. Applications of enantioselective halolactonization reactions, synthesis of photocaged compounds for identifying neurons based on function, and progress towards the total synthesis of alstoscholarisine E. [Doctoral Dissertation]. University of Texas – Austin; 2018. Available from: http://hdl.handle.net/2152/68029


University of Texas – Austin

7. 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 November 15, 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. 15 Nov 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 Nov 15]. 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

8. 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 November 15, 2019. 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. 15 Nov 2019.

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 2019 Nov 15]. 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


University of Texas – Austin

9. 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 (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 November 15, 2019. http://hdl.handle.net/2152/63302.

MLA Handbook (7th Edition):

Seipp, Charles Aaron. “Guanidinium-based receptors for anion separations.” 2018. Web. 15 Nov 2019.

Vancouver:

Seipp CA. Guanidinium-based receptors for anion separations. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2018. [cited 2019 Nov 15]. 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


University of Texas – Austin

10. Hayes, Colin O'Mara. Directly-patternable benzocyclobutene dielectric materials.

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

 Silicon Valley, America’s bastion of innovation is named for the tiny pieces finely patterned silicon transistors that are the “brains” of all modern computational devices.… (more)

Subjects/Keywords: Benzocyclobutene; Mitsunobu; Norbornene; POSS; Polyimide

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APA (6th Edition):

Hayes, C. O. (2016). Directly-patternable benzocyclobutene dielectric materials. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/68215

Chicago Manual of Style (16th Edition):

Hayes, Colin O'Mara. “Directly-patternable benzocyclobutene dielectric materials.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed November 15, 2019. http://hdl.handle.net/2152/68215.

MLA Handbook (7th Edition):

Hayes, Colin O'Mara. “Directly-patternable benzocyclobutene dielectric materials.” 2016. Web. 15 Nov 2019.

Vancouver:

Hayes CO. Directly-patternable benzocyclobutene dielectric materials. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/2152/68215.

Council of Science Editors:

Hayes CO. Directly-patternable benzocyclobutene dielectric materials. [Doctoral Dissertation]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/68215


University of Texas – Austin

11. -7566-6999. Thermodynamic analysis of protein-ligand interactions of linear tripeptide HCV NS3 protease inhibitors and progress toward the total synthesis of (±)-arboridinine.

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

 Interactions between proteins and small molecules dictate an overwhelmingly large number of biological processes, yet our knowledge of the effects of ligand structural changes on… (more)

Subjects/Keywords: Organic synthesis; Natural product; Protein-ligand interactions; Thermodynamics

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APA (6th Edition):

-7566-6999. (2017). Thermodynamic analysis of protein-ligand interactions of linear tripeptide HCV NS3 protease inhibitors and progress toward the total synthesis of (±)-arboridinine. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/63464

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

Chicago Manual of Style (16th Edition):

-7566-6999. “Thermodynamic analysis of protein-ligand interactions of linear tripeptide HCV NS3 protease inhibitors and progress toward the total synthesis of (±)-arboridinine.” 2017. Doctoral Dissertation, University of Texas – Austin. Accessed November 15, 2019. http://hdl.handle.net/2152/63464.

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

MLA Handbook (7th Edition):

-7566-6999. “Thermodynamic analysis of protein-ligand interactions of linear tripeptide HCV NS3 protease inhibitors and progress toward the total synthesis of (±)-arboridinine.” 2017. Web. 15 Nov 2019.

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

Vancouver:

-7566-6999. Thermodynamic analysis of protein-ligand interactions of linear tripeptide HCV NS3 protease inhibitors and progress toward the total synthesis of (±)-arboridinine. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2017. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/2152/63464.

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

Council of Science Editors:

-7566-6999. Thermodynamic analysis of protein-ligand interactions of linear tripeptide HCV NS3 protease inhibitors and progress toward the total synthesis of (±)-arboridinine. [Doctoral Dissertation]. University of Texas – Austin; 2017. Available from: http://hdl.handle.net/2152/63464

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


University of Texas – Austin

12. 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 November 15, 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. 15 Nov 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 Nov 15]. 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

13. -5909-4924. Modification of N-heterocyclic carbene scaffolds : insights into reactivity and electronic properties.

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

 Starting from the initial efforts to prepare, study, and utilize carbenes, the choice of substituents has been recognized as a critical factor in determining their… (more)

Subjects/Keywords: Carbenes; Stable carbenes; Electrophilic carbenes

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APA (6th Edition):

-5909-4924. (2017). Modification of N-heterocyclic carbene scaffolds : insights into reactivity and electronic properties. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/72807

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-5909-4924. “Modification of N-heterocyclic carbene scaffolds : insights into reactivity and electronic properties.” 2017. Doctoral Dissertation, University of Texas – Austin. Accessed November 15, 2019. http://hdl.handle.net/2152/72807.

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

MLA Handbook (7th Edition):

-5909-4924. “Modification of N-heterocyclic carbene scaffolds : insights into reactivity and electronic properties.” 2017. Web. 15 Nov 2019.

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

Vancouver:

-5909-4924. Modification of N-heterocyclic carbene scaffolds : insights into reactivity and electronic properties. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2017. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/2152/72807.

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

Council of Science Editors:

-5909-4924. Modification of N-heterocyclic carbene scaffolds : insights into reactivity and electronic properties. [Doctoral Dissertation]. University of Texas – Austin; 2017. Available from: http://hdl.handle.net/2152/72807

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Author name may be incomplete


University of Texas – Austin

14. Chen, Penghao. Transition metal catalyzed carbon-carbon bond activation : from four-membered rings to less-strained systems.

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

 With the help of trasition metal catalysis, a number of previously considered inert moieties can be readily functionalized. We show special interest in carbon-carbon bond… (more)

Subjects/Keywords: Transition metal catalysis; Carbon-carbon bond activation

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APA (6th Edition):

Chen, P. (2017). Transition metal catalyzed carbon-carbon bond activation : from four-membered rings to less-strained systems. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/3129

Chicago Manual of Style (16th Edition):

Chen, Penghao. “Transition metal catalyzed carbon-carbon bond activation : from four-membered rings to less-strained systems.” 2017. Doctoral Dissertation, University of Texas – Austin. Accessed November 15, 2019. http://dx.doi.org/10.26153/tsw/3129.

MLA Handbook (7th Edition):

Chen, Penghao. “Transition metal catalyzed carbon-carbon bond activation : from four-membered rings to less-strained systems.” 2017. Web. 15 Nov 2019.

Vancouver:

Chen P. Transition metal catalyzed carbon-carbon bond activation : from four-membered rings to less-strained systems. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2017. [cited 2019 Nov 15]. Available from: http://dx.doi.org/10.26153/tsw/3129.

Council of Science Editors:

Chen P. Transition metal catalyzed carbon-carbon bond activation : from four-membered rings to less-strained systems. [Doctoral Dissertation]. University of Texas – Austin; 2017. Available from: http://dx.doi.org/10.26153/tsw/3129

15. Myslinski, James Michael. Design, synthesis, and calorimetric studies on protein-ligand interactions : apolar surface area, conformational constraints, and cation-[pi] interactions.

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

 Because bimolecular interactions in water are poorly understood, three tactics commonly used to improve binding affinity in ligand design were investigated: (1) increasing apolar surface… (more)

Subjects/Keywords: Protein-ligand; Cation-[pi]; Interactions; Biomolecules; Biochemistry; Biophysical; Chemistry

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APA (6th Edition):

Myslinski, J. M. (2013). Design, synthesis, and calorimetric studies on protein-ligand interactions : apolar surface area, conformational constraints, and cation-[pi] interactions. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/25115

Chicago Manual of Style (16th Edition):

Myslinski, James Michael. “Design, synthesis, and calorimetric studies on protein-ligand interactions : apolar surface area, conformational constraints, and cation-[pi] interactions.” 2013. Doctoral Dissertation, University of Texas – Austin. Accessed November 15, 2019. http://hdl.handle.net/2152/25115.

MLA Handbook (7th Edition):

Myslinski, James Michael. “Design, synthesis, and calorimetric studies on protein-ligand interactions : apolar surface area, conformational constraints, and cation-[pi] interactions.” 2013. Web. 15 Nov 2019.

Vancouver:

Myslinski JM. Design, synthesis, and calorimetric studies on protein-ligand interactions : apolar surface area, conformational constraints, and cation-[pi] interactions. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2013. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/2152/25115.

Council of Science Editors:

Myslinski JM. Design, synthesis, and calorimetric studies on protein-ligand interactions : apolar surface area, conformational constraints, and cation-[pi] interactions. [Doctoral Dissertation]. University of Texas – Austin; 2013. Available from: http://hdl.handle.net/2152/25115

16. Amorde, Shawn Marie. A cascade approach toward indolizidine and quinolizidine alkaloids : highlighted by the total syntheses of (±)-epilupinine, (±)-tashiromine, and (-)-epimyrtine progress toward the total synthesis of (±)-meloscine.

Degree: PhD, Chemistry, 2006, University of Texas – Austin

 Several novel cascade processes have been designed and developed that involve sequential reactions of imines and iminium ions to form substituted quinolizidine ring systems in… (more)

Subjects/Keywords: Quinolizidine alkaloids; Meloscine; Indoles; Synthesis

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APA (6th Edition):

Amorde, S. M. (2006). A cascade approach toward indolizidine and quinolizidine alkaloids : highlighted by the total syntheses of (±)-epilupinine, (±)-tashiromine, and (-)-epimyrtine progress toward the total synthesis of (±)-meloscine. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/20987

Chicago Manual of Style (16th Edition):

Amorde, Shawn Marie. “A cascade approach toward indolizidine and quinolizidine alkaloids : highlighted by the total syntheses of (±)-epilupinine, (±)-tashiromine, and (-)-epimyrtine progress toward the total synthesis of (±)-meloscine.” 2006. Doctoral Dissertation, University of Texas – Austin. Accessed November 15, 2019. http://hdl.handle.net/2152/20987.

MLA Handbook (7th Edition):

Amorde, Shawn Marie. “A cascade approach toward indolizidine and quinolizidine alkaloids : highlighted by the total syntheses of (±)-epilupinine, (±)-tashiromine, and (-)-epimyrtine progress toward the total synthesis of (±)-meloscine.” 2006. Web. 15 Nov 2019.

Vancouver:

Amorde SM. A cascade approach toward indolizidine and quinolizidine alkaloids : highlighted by the total syntheses of (±)-epilupinine, (±)-tashiromine, and (-)-epimyrtine progress toward the total synthesis of (±)-meloscine. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2006. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/2152/20987.

Council of Science Editors:

Amorde SM. A cascade approach toward indolizidine and quinolizidine alkaloids : highlighted by the total syntheses of (±)-epilupinine, (±)-tashiromine, and (-)-epimyrtine progress toward the total synthesis of (±)-meloscine. [Doctoral Dissertation]. University of Texas – Austin; 2006. Available from: http://hdl.handle.net/2152/20987

17. Del Valle, David John. Total synthesis of C17-benzene ansamycins via carbon-carbon bond forming hydrogenations.

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

 Ansamycin natural products have historically been a rich source of new drugs for the treatment of bacterial infections and cancer. The C17-benzene ansamycins in particular… (more)

Subjects/Keywords: C-C bond forming hydrogenation; Ansamycin; Natural product synthesis; Metathesis

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APA (6th Edition):

Del Valle, D. J. (2013). Total synthesis of C17-benzene ansamycins via carbon-carbon bond forming hydrogenations. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/23479

Chicago Manual of Style (16th Edition):

Del Valle, David John. “Total synthesis of C17-benzene ansamycins via carbon-carbon bond forming hydrogenations.” 2013. Doctoral Dissertation, University of Texas – Austin. Accessed November 15, 2019. http://hdl.handle.net/2152/23479.

MLA Handbook (7th Edition):

Del Valle, David John. “Total synthesis of C17-benzene ansamycins via carbon-carbon bond forming hydrogenations.” 2013. Web. 15 Nov 2019.

Vancouver:

Del Valle DJ. Total synthesis of C17-benzene ansamycins via carbon-carbon bond forming hydrogenations. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2013. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/2152/23479.

Council of Science Editors:

Del Valle DJ. Total synthesis of C17-benzene ansamycins via carbon-carbon bond forming hydrogenations. [Doctoral Dissertation]. University of Texas – Austin; 2013. Available from: http://hdl.handle.net/2152/23479

18. Bonaparte, Amy C. Synthesis of [beta]-heteroaryl propionates via trapping of carbocations with [pi]-nucleophiles, efforts towards the total synthesis of acutumine, and the design, synthesis, and thermodynamics of protein-ligand interactions at the Src SH2 domain.

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

 Heterocyclic alcohols were coupled with [pi]-nucleophiles in the presence of trimethylsilyl trifluoromethanesulfonate to provide a variety of substituted [beta]-heteroaryl propionates, including those with contiguous quaternary… (more)

Subjects/Keywords: Organic chemistry

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APA (6th Edition):

Bonaparte, A. C. (2013). Synthesis of [beta]-heteroaryl propionates via trapping of carbocations with [pi]-nucleophiles, efforts towards the total synthesis of acutumine, and the design, synthesis, and thermodynamics of protein-ligand interactions at the Src SH2 domain. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/23475

Chicago Manual of Style (16th Edition):

Bonaparte, Amy C. “Synthesis of [beta]-heteroaryl propionates via trapping of carbocations with [pi]-nucleophiles, efforts towards the total synthesis of acutumine, and the design, synthesis, and thermodynamics of protein-ligand interactions at the Src SH2 domain.” 2013. Doctoral Dissertation, University of Texas – Austin. Accessed November 15, 2019. http://hdl.handle.net/2152/23475.

MLA Handbook (7th Edition):

Bonaparte, Amy C. “Synthesis of [beta]-heteroaryl propionates via trapping of carbocations with [pi]-nucleophiles, efforts towards the total synthesis of acutumine, and the design, synthesis, and thermodynamics of protein-ligand interactions at the Src SH2 domain.” 2013. Web. 15 Nov 2019.

Vancouver:

Bonaparte AC. Synthesis of [beta]-heteroaryl propionates via trapping of carbocations with [pi]-nucleophiles, efforts towards the total synthesis of acutumine, and the design, synthesis, and thermodynamics of protein-ligand interactions at the Src SH2 domain. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2013. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/2152/23475.

Council of Science Editors:

Bonaparte AC. Synthesis of [beta]-heteroaryl propionates via trapping of carbocations with [pi]-nucleophiles, efforts towards the total synthesis of acutumine, and the design, synthesis, and thermodynamics of protein-ligand interactions at the Src SH2 domain. [Doctoral Dissertation]. University of Texas – Austin; 2013. Available from: http://hdl.handle.net/2152/23475


University of Texas – Austin

19. Reichelt, Andreas. Studies on the viability of cyclopropane-containing peptidomimetics and application of the vinylogous Mannich reaction to the syntheses of indolizidine natural products.

Degree: PhD, Chemistry, 2003, University of Texas – Austin

 1,2,3-Trisubstituted cyclopropanes have been previously incorporated into inhibitors of matrix metalloproteases, in order to mimic extended conformations of the peptide backbones and orient the amino… (more)

Subjects/Keywords: Cyclopropane; Peptides – Synthesis; Mannich reaction

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APA (6th Edition):

Reichelt, A. (2003). Studies on the viability of cyclopropane-containing peptidomimetics and application of the vinylogous Mannich reaction to the syntheses of indolizidine natural products. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/882

Chicago Manual of Style (16th Edition):

Reichelt, Andreas. “Studies on the viability of cyclopropane-containing peptidomimetics and application of the vinylogous Mannich reaction to the syntheses of indolizidine natural products.” 2003. Doctoral Dissertation, University of Texas – Austin. Accessed November 15, 2019. http://hdl.handle.net/2152/882.

MLA Handbook (7th Edition):

Reichelt, Andreas. “Studies on the viability of cyclopropane-containing peptidomimetics and application of the vinylogous Mannich reaction to the syntheses of indolizidine natural products.” 2003. Web. 15 Nov 2019.

Vancouver:

Reichelt A. Studies on the viability of cyclopropane-containing peptidomimetics and application of the vinylogous Mannich reaction to the syntheses of indolizidine natural products. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2003. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/2152/882.

Council of Science Editors:

Reichelt A. Studies on the viability of cyclopropane-containing peptidomimetics and application of the vinylogous Mannich reaction to the syntheses of indolizidine natural products. [Doctoral Dissertation]. University of Texas – Austin; 2003. Available from: http://hdl.handle.net/2152/882


University of Texas – Austin

20. Kaelin, David Earl. Novel methodologies for the synthesis of C-aryl glycosides and progress toward the synthesis of the C-aryl glycoside natural products galtamycinone and kidamycin.

Degree: PhD, Chemistry, 2002, University of Texas – Austin

 The development of methodologies for the synthesis of C-aryl glycosides has been described. Novel C-aryl glycosides were prepared by [4+2] cycloadditions between benzynes and glycosyl-substituted… (more)

Subjects/Keywords: Glycosides – Synthesis; Antineoplastic antibiotics

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APA (6th Edition):

Kaelin, D. E. (2002). Novel methodologies for the synthesis of C-aryl glycosides and progress toward the synthesis of the C-aryl glycoside natural products galtamycinone and kidamycin. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/686

Chicago Manual of Style (16th Edition):

Kaelin, David Earl. “Novel methodologies for the synthesis of C-aryl glycosides and progress toward the synthesis of the C-aryl glycoside natural products galtamycinone and kidamycin.” 2002. Doctoral Dissertation, University of Texas – Austin. Accessed November 15, 2019. http://hdl.handle.net/2152/686.

MLA Handbook (7th Edition):

Kaelin, David Earl. “Novel methodologies for the synthesis of C-aryl glycosides and progress toward the synthesis of the C-aryl glycoside natural products galtamycinone and kidamycin.” 2002. Web. 15 Nov 2019.

Vancouver:

Kaelin DE. Novel methodologies for the synthesis of C-aryl glycosides and progress toward the synthesis of the C-aryl glycoside natural products galtamycinone and kidamycin. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2002. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/2152/686.

Council of Science Editors:

Kaelin DE. Novel methodologies for the synthesis of C-aryl glycosides and progress toward the synthesis of the C-aryl glycoside natural products galtamycinone and kidamycin. [Doctoral Dissertation]. University of Texas – Austin; 2002. Available from: http://hdl.handle.net/2152/686

21. 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 November 15, 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. 15 Nov 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 Nov 15]. 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

22. 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 November 15, 2019. 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. 15 Nov 2019.

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 2019 Nov 15]. 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

23. Wang, Gang, Ph. D. Transition-metal-catalyzed C-C bonds formation via transfer hydrogenation : from methodology development to (+)-SCH 351448 synthesis.

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

 Redox-triggered carbonyl addition via transfer hydrogenation, which enables direct primary alcohol C-H functionalization to form C-C bond, avoids usage of premetalated reagents or discrete alcohol… (more)

Subjects/Keywords: Transition-metal-catalyzed; C-C bonds formation; Transfer hydrogenation; Total synthesis

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APA (6th Edition):

Wang, Gang, P. D. (2017). Transition-metal-catalyzed C-C bonds formation via transfer hydrogenation : from methodology development to (+)-SCH 351448 synthesis. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/61815

Chicago Manual of Style (16th Edition):

Wang, Gang, Ph D. “Transition-metal-catalyzed C-C bonds formation via transfer hydrogenation : from methodology development to (+)-SCH 351448 synthesis.” 2017. Doctoral Dissertation, University of Texas – Austin. Accessed November 15, 2019. http://hdl.handle.net/2152/61815.

MLA Handbook (7th Edition):

Wang, Gang, Ph D. “Transition-metal-catalyzed C-C bonds formation via transfer hydrogenation : from methodology development to (+)-SCH 351448 synthesis.” 2017. Web. 15 Nov 2019.

Vancouver:

Wang, Gang PD. Transition-metal-catalyzed C-C bonds formation via transfer hydrogenation : from methodology development to (+)-SCH 351448 synthesis. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2017. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/2152/61815.

Council of Science Editors:

Wang, Gang PD. Transition-metal-catalyzed C-C bonds formation via transfer hydrogenation : from methodology development to (+)-SCH 351448 synthesis. [Doctoral Dissertation]. University of Texas – Austin; 2017. Available from: http://hdl.handle.net/2152/61815

.