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You searched for +publisher:"University of Texas – Austin" +contributor:("Krische, Michael J."). Showing records 1 – 23 of 23 total matches.

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University of Texas – Austin

1. -4843-2158. Transition metal-catalyzed redox-triggered C-C couplings of alcohols via transfer hydrogenation.

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

 In the first chapter, the first example of transfer hydrogenative cross-couplings of styrene with primary alcohols is reported. Using RuHCl(CO)(PCy₃)₂ as the precatalyst, AgOTf or… (more)

Subjects/Keywords: C-C coupling; Transfer hydrogenation

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APA (6th Edition):

-4843-2158. (2018). Transition metal-catalyzed redox-triggered C-C couplings of alcohols via transfer hydrogenation. (Masters Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/63545

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-4843-2158. “Transition metal-catalyzed redox-triggered C-C couplings of alcohols via transfer hydrogenation.” 2018. Masters Thesis, University of Texas – Austin. Accessed October 14, 2019. http://hdl.handle.net/2152/63545.

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

MLA Handbook (7th Edition):

-4843-2158. “Transition metal-catalyzed redox-triggered C-C couplings of alcohols via transfer hydrogenation.” 2018. Web. 14 Oct 2019.

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

Vancouver:

-4843-2158. Transition metal-catalyzed redox-triggered C-C couplings of alcohols via transfer hydrogenation. [Internet] [Masters thesis]. University of Texas – Austin; 2018. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/2152/63545.

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

Council of Science Editors:

-4843-2158. Transition metal-catalyzed redox-triggered C-C couplings of alcohols via transfer hydrogenation. [Masters Thesis]. University of Texas – Austin; 2018. Available from: http://hdl.handle.net/2152/63545

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


University of Texas – Austin

2. Zhang, Wandi. Transition-metal catalyzed redox triggered C-C bond forming reactions via carbonyl addition.

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

 Carbon-carbon (C–C) bonds construct the skeleton of all organic molecules. Hence, the development of new efficient methods of C–C bond formation is of great significance… (more)

Subjects/Keywords: Transition metal catalysis; Carbonyl addition; C-C bond forming reaction

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APA (6th Edition):

Zhang, W. (2019). Transition-metal catalyzed redox triggered C-C bond forming reactions via carbonyl addition. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/2273

Chicago Manual of Style (16th Edition):

Zhang, Wandi. “Transition-metal catalyzed redox triggered C-C bond forming reactions via carbonyl addition.” 2019. Doctoral Dissertation, University of Texas – Austin. Accessed October 14, 2019. http://dx.doi.org/10.26153/tsw/2273.

MLA Handbook (7th Edition):

Zhang, Wandi. “Transition-metal catalyzed redox triggered C-C bond forming reactions via carbonyl addition.” 2019. Web. 14 Oct 2019.

Vancouver:

Zhang W. Transition-metal catalyzed redox triggered C-C bond forming reactions via carbonyl addition. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2019. [cited 2019 Oct 14]. Available from: http://dx.doi.org/10.26153/tsw/2273.

Council of Science Editors:

Zhang W. Transition-metal catalyzed redox triggered C-C bond forming reactions via carbonyl addition. [Doctoral Dissertation]. University of Texas – Austin; 2019. Available from: http://dx.doi.org/10.26153/tsw/2273


University of Texas – Austin

3. Kim, Mary M. Towards the synthesis of notoamide C.

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

 Members of the prenylated indole alkaloid family have attracted much attention from synthetic chemists and drug developers for their distinct structural complexity and diverse bioactivity.… (more)

Subjects/Keywords: Reverse prenylation; Notoamide C

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APA (6th Edition):

Kim, M. M. (2013). Towards the synthesis of notoamide C. (Masters Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/41447

Chicago Manual of Style (16th Edition):

Kim, Mary M. “Towards the synthesis of notoamide C.” 2013. Masters Thesis, University of Texas – Austin. Accessed October 14, 2019. http://hdl.handle.net/2152/41447.

MLA Handbook (7th Edition):

Kim, Mary M. “Towards the synthesis of notoamide C.” 2013. Web. 14 Oct 2019.

Vancouver:

Kim MM. Towards the synthesis of notoamide C. [Internet] [Masters thesis]. University of Texas – Austin; 2013. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/2152/41447.

Council of Science Editors:

Kim MM. Towards the synthesis of notoamide C. [Masters Thesis]. University of Texas – Austin; 2013. Available from: http://hdl.handle.net/2152/41447

4. Leung, Joyce Chi Ching. Transition metal catalyzed C-C bond formation under transfer hydrogenation conditions.

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

 Carbon-carbon bond forming reactions are fundamental transformations for constructing structurally complex organic building blocks, especially in the realm of natural products synthesis. Classical protocols for… (more)

Subjects/Keywords: Organometallic; Transition metal; Catalysis; Hydrogenation; Hydrogenative; Carbonyl additions; Stereoselective

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APA (6th Edition):

Leung, J. C. C. (2013). Transition metal catalyzed C-C bond formation under transfer hydrogenation conditions. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/21527

Chicago Manual of Style (16th Edition):

Leung, Joyce Chi Ching. “Transition metal catalyzed C-C bond formation under transfer hydrogenation conditions.” 2013. Doctoral Dissertation, University of Texas – Austin. Accessed October 14, 2019. http://hdl.handle.net/2152/21527.

MLA Handbook (7th Edition):

Leung, Joyce Chi Ching. “Transition metal catalyzed C-C bond formation under transfer hydrogenation conditions.” 2013. Web. 14 Oct 2019.

Vancouver:

Leung JCC. Transition metal catalyzed C-C bond formation under transfer hydrogenation conditions. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2013. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/2152/21527.

Council of Science Editors:

Leung JCC. Transition metal catalyzed C-C bond formation under transfer hydrogenation conditions. [Doctoral Dissertation]. University of Texas – Austin; 2013. Available from: http://hdl.handle.net/2152/21527

5. Lu, Yu, active 2012. Carbon-carbon bond formation via catalytic hydrogenation and transfer hydrogenation : application in the total synthesis of bryostatin 7.

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

 Under the conditions of transfer hydrogenation employing ortho-cyclometallated iridium C,O-benzoate catalysts, two protocols of iterative chain elongation of 1,3-diols to furnish 1,3-polyols were developed. First,… (more)

Subjects/Keywords: Catalytic; Carbon-carbon bond formation; Allylation; Hydrogenation; Transfer hydrogenation; 1,3-polyols; Polyketides; Bryostatin; Total synthesis

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APA (6th Edition):

Lu, Yu, a. 2. (2012). Carbon-carbon bond formation via catalytic hydrogenation and transfer hydrogenation : application in the total synthesis of bryostatin 7. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/22149

Chicago Manual of Style (16th Edition):

Lu, Yu, active 2012. “Carbon-carbon bond formation via catalytic hydrogenation and transfer hydrogenation : application in the total synthesis of bryostatin 7.” 2012. Doctoral Dissertation, University of Texas – Austin. Accessed October 14, 2019. http://hdl.handle.net/2152/22149.

MLA Handbook (7th Edition):

Lu, Yu, active 2012. “Carbon-carbon bond formation via catalytic hydrogenation and transfer hydrogenation : application in the total synthesis of bryostatin 7.” 2012. Web. 14 Oct 2019.

Vancouver:

Lu, Yu a2. Carbon-carbon bond formation via catalytic hydrogenation and transfer hydrogenation : application in the total synthesis of bryostatin 7. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2012. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/2152/22149.

Council of Science Editors:

Lu, Yu a2. Carbon-carbon bond formation via catalytic hydrogenation and transfer hydrogenation : application in the total synthesis of bryostatin 7. [Doctoral Dissertation]. University of Texas – Austin; 2012. Available from: http://hdl.handle.net/2152/22149


University of Texas – Austin

6. -1902-3184. Transition metal catalyzed redox triggered C–C bond forming reactions of alcohols via transfer hydrogenation.

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

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

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

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

-1902-3184. “Transition metal catalyzed redox triggered C–C bond forming reactions of alcohols via transfer hydrogenation.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed October 14, 2019. http://hdl.handle.net/2152/46996.

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

MLA Handbook (7th Edition):

-1902-3184. “Transition metal catalyzed redox triggered C–C bond forming reactions of alcohols via transfer hydrogenation.” 2016. Web. 14 Oct 2019.

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

Vancouver:

-1902-3184. Transition metal catalyzed redox triggered C–C bond forming reactions of alcohols via transfer hydrogenation. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/2152/46996.

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

Council of Science Editors:

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

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


University of Texas – Austin

7. -2419-9854. Development of neutral redox carbon-carbon bond forming reactions via transition metal-catalyzed transfer hydrogenation.

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

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

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

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APA (6th Edition):

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

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-2419-9854. “Development of neutral redox carbon-carbon bond forming reactions via transition metal-catalyzed transfer hydrogenation.” 2018. Doctoral Dissertation, University of Texas – Austin. Accessed October 14, 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. 14 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 14]. 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

8. -7981-5709. Rhodium(I)-catalyzed C–C bond activation : decarbonylation of α,β-acetylenic ketones: Rhodium(I)-catalyzed C–C bond activation : decarbonylation of [alpha], [beta]-acetylenic ketones.

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

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

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

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

-7981-5709. “Rhodium(I)-catalyzed C–C bond activation : decarbonylation of α,β-acetylenic ketones: Rhodium(I)-catalyzed C–C bond activation : decarbonylation of [alpha], [beta]-acetylenic ketones.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed October 14, 2019. http://hdl.handle.net/2152/40932.

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

MLA Handbook (7th Edition):

-7981-5709. “Rhodium(I)-catalyzed C–C bond activation : decarbonylation of α,β-acetylenic ketones: Rhodium(I)-catalyzed C–C bond activation : decarbonylation of [alpha], [beta]-acetylenic ketones.” 2016. Web. 14 Oct 2019.

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

Vancouver:

-7981-5709. Rhodium(I)-catalyzed C–C bond activation : decarbonylation of α,β-acetylenic ketones: Rhodium(I)-catalyzed C–C bond activation : decarbonylation of [alpha], [beta]-acetylenic ketones. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/2152/40932.

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

Council of Science Editors:

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

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Author name may be incomplete


University of Texas – Austin

9. 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 October 14, 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. 14 Oct 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 Oct 14]. 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

10. Davis, Christina Marie. Electron transfer within tetrathiafulvalene calix[4]pyrrole supramolecular ensembles.

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

 Over the last decade, the ecological need for clean and renewable energy sources has resulted in considerable resources being directed toward the development of systems… (more)

Subjects/Keywords: Tetrathiafulvalene Calix[4]pyrrole; Electron transfer; Supramolecular chemistry

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APA (6th Edition):

Davis, C. M. (2014). Electron transfer within tetrathiafulvalene calix[4]pyrrole supramolecular ensembles. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/46525

Chicago Manual of Style (16th Edition):

Davis, Christina Marie. “Electron transfer within tetrathiafulvalene calix[4]pyrrole supramolecular ensembles.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed October 14, 2019. http://hdl.handle.net/2152/46525.

MLA Handbook (7th Edition):

Davis, Christina Marie. “Electron transfer within tetrathiafulvalene calix[4]pyrrole supramolecular ensembles.” 2014. Web. 14 Oct 2019.

Vancouver:

Davis CM. Electron transfer within tetrathiafulvalene calix[4]pyrrole supramolecular ensembles. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/2152/46525.

Council of Science Editors:

Davis CM. Electron transfer within tetrathiafulvalene calix[4]pyrrole supramolecular ensembles. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/46525


University of Texas – Austin

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

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

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Ren, Zhi. “Palladium-catalyzed carbon-hydrogen bond functionalization utilizing an exo-directing strategy.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed October 14, 2019. http://hdl.handle.net/2152/39758.

MLA Handbook (7th Edition):

Ren, Zhi. “Palladium-catalyzed carbon-hydrogen bond functionalization utilizing an exo-directing strategy.” 2016. Web. 14 Oct 2019.

Vancouver:

Ren Z. Palladium-catalyzed carbon-hydrogen bond functionalization utilizing an exo-directing strategy. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/2152/39758.

Council of Science Editors:

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


University of Texas – Austin

12. -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

Note: this citation may be lacking information needed for this citation format:
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 October 14, 2019. 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. 14 Oct 2019.

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 2019 Oct 14]. 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

13. -6179-7645. Transition metal catalyzed C-C bond formation via transfer hydrogenation : from methodology development to polycyclic aromatic hydrocarbon syntheses.

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

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

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

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APA (6th Edition):

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

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-6179-7645. “Transition metal catalyzed C-C bond formation via transfer hydrogenation : from methodology development to polycyclic aromatic hydrocarbon syntheses.” 2019. Doctoral Dissertation, University of Texas – Austin. Accessed October 14, 2019. http://dx.doi.org/10.26153/tsw/2170.

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

MLA Handbook (7th Edition):

-6179-7645. “Transition metal catalyzed C-C bond formation via transfer hydrogenation : from methodology development to polycyclic aromatic hydrocarbon syntheses.” 2019. Web. 14 Oct 2019.

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

Vancouver:

-6179-7645. Transition metal catalyzed C-C bond formation via transfer hydrogenation : from methodology development to polycyclic aromatic hydrocarbon syntheses. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2019. [cited 2019 Oct 14]. Available from: http://dx.doi.org/10.26153/tsw/2170.

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

Council of Science Editors:

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

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


University of Texas – Austin

14. 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 14, 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. 14 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 14]. 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

15. 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 14, 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. 14 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 14]. 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

16. -6302-5569. Novel multifunctional porous coordination polymers from pre-synthetically modified organophosphorus ligands.

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

 Phosphine-based Porous Coordination Polymers (PCPs) have shown promising results as gas storage, gas separations, and molecular sensing materials due the versatility of the P(III)/P(V) chemistry,… (more)

Subjects/Keywords: Porous coordination polymers; Metal-organic frameworks; Phosphine coordination materials

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APA (6th Edition):

-6302-5569. (2015). Novel multifunctional porous coordination polymers from pre-synthetically modified organophosphorus ligands. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/46714

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-6302-5569. “Novel multifunctional porous coordination polymers from pre-synthetically modified organophosphorus ligands.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed October 14, 2019. http://hdl.handle.net/2152/46714.

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

MLA Handbook (7th Edition):

-6302-5569. “Novel multifunctional porous coordination polymers from pre-synthetically modified organophosphorus ligands.” 2015. Web. 14 Oct 2019.

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

Vancouver:

-6302-5569. Novel multifunctional porous coordination polymers from pre-synthetically modified organophosphorus ligands. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/2152/46714.

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

Council of Science Editors:

-6302-5569. Novel multifunctional porous coordination polymers from pre-synthetically modified organophosphorus ligands. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/46714

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


University of Texas – Austin

17. Silver, Eric Scott. Studies in anion-responsive polymers and 6-shogaol as a chemopreventive of prostate cancer.

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

 The study of the binding and recognition of anions has emerged as a significant branch of supramolecular chemistry over the past 20 years. Of particular… (more)

Subjects/Keywords: Anion binding; Polymers; 6-shogaol; Prostate cancer; Calix[4]pyrrole; Quinoxaline; Fluoride sensing; Chemopreventive

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APA (6th Edition):

Silver, E. S. (2014). Studies in anion-responsive polymers and 6-shogaol as a chemopreventive of prostate cancer. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/31326

Chicago Manual of Style (16th Edition):

Silver, Eric Scott. “Studies in anion-responsive polymers and 6-shogaol as a chemopreventive of prostate cancer.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed October 14, 2019. http://hdl.handle.net/2152/31326.

MLA Handbook (7th Edition):

Silver, Eric Scott. “Studies in anion-responsive polymers and 6-shogaol as a chemopreventive of prostate cancer.” 2014. Web. 14 Oct 2019.

Vancouver:

Silver ES. Studies in anion-responsive polymers and 6-shogaol as a chemopreventive of prostate cancer. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/2152/31326.

Council of Science Editors:

Silver ES. Studies in anion-responsive polymers and 6-shogaol as a chemopreventive of prostate cancer. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/31326


University of Texas – Austin

18. 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 14, 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. 14 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 14]. 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

19. Luis, Ana Liza. Transition metal- and organo-catalyzed cycloreductions, cycloadditions and cycloisomerizations.

Degree: PhD, Chemistry, 2005, University of Texas – Austin

 The catalytic activation of enones in C-C bond forming processes represents a promising alternative to the prefabrication of chemically labile enols and enolates. Through the… (more)

Subjects/Keywords: Transition metals; Organo-catalyzed cycloreductions; Organo-catalyzed cycloadditions; Organo-catalyzed cycloisomerizations; C-C bond; Enones; Cycloisomerization of bis-enones

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APA (6th Edition):

Luis, A. L. (2005). Transition metal- and organo-catalyzed cycloreductions, cycloadditions and cycloisomerizations. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/29634

Chicago Manual of Style (16th Edition):

Luis, Ana Liza. “Transition metal- and organo-catalyzed cycloreductions, cycloadditions and cycloisomerizations.” 2005. Doctoral Dissertation, University of Texas – Austin. Accessed October 14, 2019. http://hdl.handle.net/2152/29634.

MLA Handbook (7th Edition):

Luis, Ana Liza. “Transition metal- and organo-catalyzed cycloreductions, cycloadditions and cycloisomerizations.” 2005. Web. 14 Oct 2019.

Vancouver:

Luis AL. Transition metal- and organo-catalyzed cycloreductions, cycloadditions and cycloisomerizations. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2005. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/2152/29634.

Council of Science Editors:

Luis AL. Transition metal- and organo-catalyzed cycloreductions, cycloadditions and cycloisomerizations. [Doctoral Dissertation]. University of Texas – Austin; 2005. Available from: http://hdl.handle.net/2152/29634


University of Texas – Austin

20. Jung, Cheol-Kyu. Phosphine-mediated furan formations and hydrogen-mediated reductive aldol reactions.

Degree: PhD, Chemistry, 2008, University of Texas – Austin

 Aldol reactions are widely used in forming new carbon-carbon bonds. Since the discovery of the aldol condensation, controlling the relative and absolute stereochemistry in aldol… (more)

Subjects/Keywords: Furan formations; Phosphine-mediated; Reductive aldol reactions; Hydrogen-mediated; Carbon-carbon bonds; Diastereoselectivity

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APA (6th Edition):

Jung, C. (2008). Phosphine-mediated furan formations and hydrogen-mediated reductive aldol reactions. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/29613

Chicago Manual of Style (16th Edition):

Jung, Cheol-Kyu. “Phosphine-mediated furan formations and hydrogen-mediated reductive aldol reactions.” 2008. Doctoral Dissertation, University of Texas – Austin. Accessed October 14, 2019. http://hdl.handle.net/2152/29613.

MLA Handbook (7th Edition):

Jung, Cheol-Kyu. “Phosphine-mediated furan formations and hydrogen-mediated reductive aldol reactions.” 2008. Web. 14 Oct 2019.

Vancouver:

Jung C. Phosphine-mediated furan formations and hydrogen-mediated reductive aldol reactions. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2008. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/2152/29613.

Council of Science Editors:

Jung C. Phosphine-mediated furan formations and hydrogen-mediated reductive aldol reactions. [Doctoral Dissertation]. University of Texas – Austin; 2008. Available from: http://hdl.handle.net/2152/29613

21. -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

Note: this citation may be lacking information needed for this citation format:
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 14, 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. 14 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 14]. 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

22. 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 October 14, 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. 14 Oct 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 Oct 14]. 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

23. -0975-088X. Transition metal-catalyzed carbon-carbon bond formation utilizing transfer hydrogenation.

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

 A central tenant of organic synthesis is the construction of carbon-carbon bonds. One of the traditional methods for carrying out such transformations is that of… (more)

Subjects/Keywords: Transfer hydrogenation; Iridium; Ruthenium; Carbonyl addition; Pyrrolidine; Imine

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APA (6th Edition):

-0975-088X. (2015). Transition metal-catalyzed carbon-carbon bond formation utilizing transfer hydrogenation. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/30513

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

Chicago Manual of Style (16th Edition):

-0975-088X. “Transition metal-catalyzed carbon-carbon bond formation utilizing transfer hydrogenation.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed October 14, 2019. http://hdl.handle.net/2152/30513.

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

MLA Handbook (7th Edition):

-0975-088X. “Transition metal-catalyzed carbon-carbon bond formation utilizing transfer hydrogenation.” 2015. Web. 14 Oct 2019.

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

Vancouver:

-0975-088X. Transition metal-catalyzed carbon-carbon bond formation utilizing transfer hydrogenation. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/2152/30513.

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

Council of Science Editors:

-0975-088X. Transition metal-catalyzed carbon-carbon bond formation utilizing transfer hydrogenation. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/30513

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

.