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

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1. Johnson, Christopher Robert. New methods towards the synthesis of graphene nanoribbons and study of the polymerization of acetylnaphthalene.

Degree: Chemistry, 2013, University of Texas – Austin

 Chapter 1 describes work towards the synthesis of graphene nanoribbons with varying widths and edge structures. Interest in graphene comes from the high electron mobility… (more)

Subjects/Keywords: Graphene; Nanoribbon; Polymer

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APA (6th Edition):

Johnson, C. R. (2013). New methods towards the synthesis of graphene nanoribbons and study of the polymerization of acetylnaphthalene. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/26458

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Johnson, Christopher Robert. “New methods towards the synthesis of graphene nanoribbons and study of the polymerization of acetylnaphthalene.” 2013. Thesis, University of Texas – Austin. Accessed August 23, 2019. http://hdl.handle.net/2152/26458.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Johnson, Christopher Robert. “New methods towards the synthesis of graphene nanoribbons and study of the polymerization of acetylnaphthalene.” 2013. Web. 23 Aug 2019.

Vancouver:

Johnson CR. New methods towards the synthesis of graphene nanoribbons and study of the polymerization of acetylnaphthalene. [Internet] [Thesis]. University of Texas – Austin; 2013. [cited 2019 Aug 23]. Available from: http://hdl.handle.net/2152/26458.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Johnson CR. New methods towards the synthesis of graphene nanoribbons and study of the polymerization of acetylnaphthalene. [Thesis]. University of Texas – Austin; 2013. Available from: http://hdl.handle.net/2152/26458

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

2. Savage, Nikolas Alexander. Accessing fused and spirocyclic ring formations via carbon - carbon bond activation.

Degree: Chemistry, 2013, University of Texas – Austin

 Carbon-carbon bonds are ubiquitous in synthetic chemistry and constitute the skeletal backbone of a significant number of compounds. Utilizing transition metal mediated catalysis, a wide… (more)

Subjects/Keywords: C-C activation; Rhodium; Spirocycle

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

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APA (6th Edition):

Savage, N. A. (2013). Accessing fused and spirocyclic ring formations via carbon - carbon bond activation. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/23647

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Savage, Nikolas Alexander. “Accessing fused and spirocyclic ring formations via carbon - carbon bond activation.” 2013. Thesis, University of Texas – Austin. Accessed August 23, 2019. http://hdl.handle.net/2152/23647.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Savage, Nikolas Alexander. “Accessing fused and spirocyclic ring formations via carbon - carbon bond activation.” 2013. Web. 23 Aug 2019.

Vancouver:

Savage NA. Accessing fused and spirocyclic ring formations via carbon - carbon bond activation. [Internet] [Thesis]. University of Texas – Austin; 2013. [cited 2019 Aug 23]. Available from: http://hdl.handle.net/2152/23647.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Savage NA. Accessing fused and spirocyclic ring formations via carbon - carbon bond activation. [Thesis]. University of Texas – Austin; 2013. Available from: http://hdl.handle.net/2152/23647

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Texas – Austin

3. -6646-8034. Synthesis and characterization of functional polymeric materials for use in organic photovoltaics.

Degree: Chemistry, 2016, University of Texas – Austin

 Norbornene-type monomers with pendant oligothiophene donor and perylene diimide acceptor groups were synthesized and polymerized using ring-opening metathesis polymerization (ROMP) to yield donor and acceptor… (more)

Subjects/Keywords: Functional block copolymers; Donor-acceptor block copolymers; Coil-coil d-a block copolymers; Functional polymeric materials; Functional polymers for organic photovoltaic applications; Organic photovoltaic materials; Hybrid solar cell materials; Block copolymers for hybrid solar cells

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APA (6th Edition):

-6646-8034. (2016). Synthesis and characterization of functional polymeric materials for use in organic photovoltaics. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/68378

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

-6646-8034. “Synthesis and characterization of functional polymeric materials for use in organic photovoltaics.” 2016. Thesis, University of Texas – Austin. Accessed August 23, 2019. http://hdl.handle.net/2152/68378.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

-6646-8034. “Synthesis and characterization of functional polymeric materials for use in organic photovoltaics.” 2016. Web. 23 Aug 2019.

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

Vancouver:

-6646-8034. Synthesis and characterization of functional polymeric materials for use in organic photovoltaics. [Internet] [Thesis]. University of Texas – Austin; 2016. [cited 2019 Aug 23]. Available from: http://hdl.handle.net/2152/68378.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

-6646-8034. Synthesis and characterization of functional polymeric materials for use in organic photovoltaics. [Thesis]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/68378

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation


University of Texas – Austin

4. -8299-3023. Formylated dipyrromethane based phosphate derivatives receptors.

Degree: Chemistry, 2016, University of Texas – Austin

 Anions are key components in many biological and industrial processes. They play crucial roles in both health and the environment. In many cases, it is… (more)

Subjects/Keywords: Dipyrromethane; Phosphate

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APA (6th Edition):

-8299-3023. (2016). Formylated dipyrromethane based phosphate derivatives receptors. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/68388

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

-8299-3023. “Formylated dipyrromethane based phosphate derivatives receptors.” 2016. Thesis, University of Texas – Austin. Accessed August 23, 2019. http://hdl.handle.net/2152/68388.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

-8299-3023. “Formylated dipyrromethane based phosphate derivatives receptors.” 2016. Web. 23 Aug 2019.

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

Vancouver:

-8299-3023. Formylated dipyrromethane based phosphate derivatives receptors. [Internet] [Thesis]. University of Texas – Austin; 2016. [cited 2019 Aug 23]. Available from: http://hdl.handle.net/2152/68388.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

-8299-3023. Formylated dipyrromethane based phosphate derivatives receptors. [Thesis]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/68388

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation


University of Texas – Austin

5. -3473-3494. Total syntheses of the regenerative natural products vinaxanthone, xanthofulvin, and eupalinilide E.

Degree: Chemistry, 2015, University of Texas – Austin

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

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

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APA (6th Edition):

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

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

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

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

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

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

Vancouver:

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

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

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

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation


University of Texas – Austin

6. -7712-308X. Total synthesis of (–)-dihydroprotolichesterinic acid via a diastereoselective conjugate addition, development of enantioselective halocyclization reactions, and progress towards the total synthesis of jiadifenolide.

Degree: Chemistry, 2015, University of Texas – Austin

 In an effort to develop a unified route to functionalized succinic acid derivatives, a new diastereoselective conjugate addition of monoorganocuprates, Li[RCuI], to a chiral fumarate… (more)

Subjects/Keywords: Conjugate Addition; Total Synthesis; Halocyclization; Halolactonization

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APA (6th Edition):

-7712-308X. (2015). Total synthesis of (–)-dihydroprotolichesterinic acid via a diastereoselective conjugate addition, development of enantioselective halocyclization reactions, and progress towards the total synthesis of jiadifenolide. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/32938

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

-7712-308X. “Total synthesis of (–)-dihydroprotolichesterinic acid via a diastereoselective conjugate addition, development of enantioselective halocyclization reactions, and progress towards the total synthesis of jiadifenolide.” 2015. Thesis, University of Texas – Austin. Accessed August 23, 2019. http://hdl.handle.net/2152/32938.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

-7712-308X. “Total synthesis of (–)-dihydroprotolichesterinic acid via a diastereoselective conjugate addition, development of enantioselective halocyclization reactions, and progress towards the total synthesis of jiadifenolide.” 2015. Web. 23 Aug 2019.

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

Vancouver:

-7712-308X. Total synthesis of (–)-dihydroprotolichesterinic acid via a diastereoselective conjugate addition, development of enantioselective halocyclization reactions, and progress towards the total synthesis of jiadifenolide. [Internet] [Thesis]. University of Texas – Austin; 2015. [cited 2019 Aug 23]. Available from: http://hdl.handle.net/2152/32938.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

-7712-308X. Total synthesis of (–)-dihydroprotolichesterinic acid via a diastereoselective conjugate addition, development of enantioselective halocyclization reactions, and progress towards the total synthesis of jiadifenolide. [Thesis]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/32938

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation


University of Texas – Austin

7. -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: 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. (Thesis). 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
Not specified: Masters Thesis or Doctoral Dissertation

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. Thesis, University of Texas – Austin. Accessed August 23, 2019. http://hdl.handle.net/2152/40932.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

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

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

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. [Thesis]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/40932

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation


University of Texas – Austin

8. -1902-3184. Transition metal catalyzed redox triggered C–C bond forming reactions of alcohols via transfer hydrogenation.

Degree: 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. (Thesis). 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
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

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

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

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

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

-1902-3184. Transition metal catalyzed redox triggered C–C bond forming reactions of alcohols via transfer hydrogenation. [Thesis]. 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
Not specified: Masters Thesis or Doctoral Dissertation


University of Texas – Austin

9. Waldeck, Andrew Robert. Development and application of metal catalyzed transfer hydrogenative C-C bond forming reactions.

Degree: Chemistry, 2016, University of Texas – Austin

 While polyketides display a diverse range of biological properties and are used extensively in human medicine, a lack of methods for the concise preparation of… (more)

Subjects/Keywords: Catalysis; Spirolactone; Total synthesis; Cyanolide; Cryptocaryol

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APA (6th Edition):

Waldeck, A. R. (2016). Development and application of metal catalyzed transfer hydrogenative C-C bond forming reactions. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/39609

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Waldeck, Andrew Robert. “Development and application of metal catalyzed transfer hydrogenative C-C bond forming reactions.” 2016. Thesis, University of Texas – Austin. Accessed August 23, 2019. http://hdl.handle.net/2152/39609.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Waldeck, Andrew Robert. “Development and application of metal catalyzed transfer hydrogenative C-C bond forming reactions.” 2016. Web. 23 Aug 2019.

Vancouver:

Waldeck AR. Development and application of metal catalyzed transfer hydrogenative C-C bond forming reactions. [Internet] [Thesis]. University of Texas – Austin; 2016. [cited 2019 Aug 23]. Available from: http://hdl.handle.net/2152/39609.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Waldeck AR. Development and application of metal catalyzed transfer hydrogenative C-C bond forming reactions. [Thesis]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/39609

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Texas – Austin

10. -8750-5428. Rhodium porphyrin alkylations with ammonium and quinolinium salts and cyclic ether formation via a palladium catalyzed dehydrogenative annulation.

Degree: Chemistry, 2016, University of Texas – Austin

 The formation and study of metal–carbon σ-bonds can help unveil unique reactivities of organometallic complexes and provide support for further catalytic transformations. Rhodium porphyrins have… (more)

Subjects/Keywords: Palladium; Directing group; Catalysis; Rhodium porphyrin; Alkylation; Cyclic ether synthesis

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APA (6th Edition):

-8750-5428. (2016). Rhodium porphyrin alkylations with ammonium and quinolinium salts and cyclic ether formation via a palladium catalyzed dehydrogenative annulation. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/39652

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

-8750-5428. “Rhodium porphyrin alkylations with ammonium and quinolinium salts and cyclic ether formation via a palladium catalyzed dehydrogenative annulation.” 2016. Thesis, University of Texas – Austin. Accessed August 23, 2019. http://hdl.handle.net/2152/39652.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

-8750-5428. “Rhodium porphyrin alkylations with ammonium and quinolinium salts and cyclic ether formation via a palladium catalyzed dehydrogenative annulation.” 2016. Web. 23 Aug 2019.

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

Vancouver:

-8750-5428. Rhodium porphyrin alkylations with ammonium and quinolinium salts and cyclic ether formation via a palladium catalyzed dehydrogenative annulation. [Internet] [Thesis]. University of Texas – Austin; 2016. [cited 2019 Aug 23]. Available from: http://hdl.handle.net/2152/39652.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

-8750-5428. Rhodium porphyrin alkylations with ammonium and quinolinium salts and cyclic ether formation via a palladium catalyzed dehydrogenative annulation. [Thesis]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/39652

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation


University of Texas – Austin

11. Yeon, Yerim. Calix[4]arene-based ion or ion-pair receptors.

Degree: Chemistry, 2018, University of Texas – Austin

 Calix[4]arene derivatives are one of the most important supramolecular scaffolds. They have been extensively exploited to build more elaborate systems. Calix[4]arene derivatives can stabilize host-guest… (more)

Subjects/Keywords: Calix[4]arene; Sensor; Colorimetric; Chromogenic; Cesium; Lithium; Graphene; Ion-pair receptor; Anion receptor

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APA (6th Edition):

Yeon, Y. (2018). Calix[4]arene-based ion or ion-pair receptors. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/71510

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Yeon, Yerim. “Calix[4]arene-based ion or ion-pair receptors.” 2018. Thesis, University of Texas – Austin. Accessed August 23, 2019. http://hdl.handle.net/2152/71510.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Yeon, Yerim. “Calix[4]arene-based ion or ion-pair receptors.” 2018. Web. 23 Aug 2019.

Vancouver:

Yeon Y. Calix[4]arene-based ion or ion-pair receptors. [Internet] [Thesis]. University of Texas – Austin; 2018. [cited 2019 Aug 23]. Available from: http://hdl.handle.net/2152/71510.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Yeon Y. Calix[4]arene-based ion or ion-pair receptors. [Thesis]. University of Texas – Austin; 2018. Available from: http://hdl.handle.net/2152/71510

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Texas – Austin

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

Degree: 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. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/68215

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Hayes, Colin O'Mara. “Directly-patternable benzocyclobutene dielectric materials.” 2016. Thesis, University of Texas – Austin. Accessed August 23, 2019. http://hdl.handle.net/2152/68215.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Hayes, Colin O'Mara. “Directly-patternable benzocyclobutene dielectric materials.” 2016. Web. 23 Aug 2019.

Vancouver:

Hayes CO. Directly-patternable benzocyclobutene dielectric materials. [Internet] [Thesis]. University of Texas – Austin; 2016. [cited 2019 Aug 23]. Available from: http://hdl.handle.net/2152/68215.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

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

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Texas – Austin

13. Liu, Di, Ph. D. Post-polymerization modification by direct C-H functionalization.

Degree: Chemistry, 2016, University of Texas – Austin

 Post-polymerization modification of polymers is an important tool for accessing macromolecular materials with desired functional groups and tailored properties. Such strategy may become the only… (more)

Subjects/Keywords: Post-polymerization modification; C-H functionalization

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APA (6th Edition):

Liu, Di, P. D. (2016). Post-polymerization modification by direct C-H functionalization. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/68263

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Liu, Di, Ph D. “Post-polymerization modification by direct C-H functionalization.” 2016. Thesis, University of Texas – Austin. Accessed August 23, 2019. http://hdl.handle.net/2152/68263.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Liu, Di, Ph D. “Post-polymerization modification by direct C-H functionalization.” 2016. Web. 23 Aug 2019.

Vancouver:

Liu, Di PD. Post-polymerization modification by direct C-H functionalization. [Internet] [Thesis]. University of Texas – Austin; 2016. [cited 2019 Aug 23]. Available from: http://hdl.handle.net/2152/68263.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Liu, Di PD. Post-polymerization modification by direct C-H functionalization. [Thesis]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/68263

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Texas – Austin

14. -9265-9181. Characterization of two radical S-adenosyl-L-methionine enzymes in the biosynthesis of aminoglycosides.

Degree: Chemistry, 2016, University of Texas – Austin

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

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

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APA (6th Edition):

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

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

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

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

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

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

Vancouver:

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

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

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

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation


University of Texas – Austin

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

Degree: 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. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/31326

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Silver, Eric Scott. “Studies in anion-responsive polymers and 6-shogaol as a chemopreventive of prostate cancer.” 2014. Thesis, University of Texas – Austin. Accessed August 23, 2019. http://hdl.handle.net/2152/31326.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Silver, Eric Scott. “Studies in anion-responsive polymers and 6-shogaol as a chemopreventive of prostate cancer.” 2014. Web. 23 Aug 2019.

Vancouver:

Silver ES. Studies in anion-responsive polymers and 6-shogaol as a chemopreventive of prostate cancer. [Internet] [Thesis]. University of Texas – Austin; 2014. [cited 2019 Aug 23]. Available from: http://hdl.handle.net/2152/31326.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

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

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Texas – Austin

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

Degree: 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. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/39758

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

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

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

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

Vancouver:

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

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

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

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Texas – Austin

17. -0166-1890. Transition metal-catalyzed transfer hydrogenative C-C bond formation : from methodology development to bryostatin analogue synthesis: Transition metal-catalyzed transfer hydrogenative carbon-carbon bond formation : from methodology development to bryostatin analogue synthesis.

Degree: Chemistry, 2016, University of Texas – Austin

 One of the more formidable challenges of organic synthesis remains the efficient construction of C-C bonds. A generally used strategy for carrying out such transformations… (more)

Subjects/Keywords: Transition-metal catalysis; Bryostatin analogue synthesis

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APA (6th Edition):

-0166-1890. (2016). Transition metal-catalyzed transfer hydrogenative C-C bond formation : from methodology development to bryostatin analogue synthesis: Transition metal-catalyzed transfer hydrogenative carbon-carbon bond formation : from methodology development to bryostatin analogue synthesis. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/41729

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

-0166-1890. “Transition metal-catalyzed transfer hydrogenative C-C bond formation : from methodology development to bryostatin analogue synthesis: Transition metal-catalyzed transfer hydrogenative carbon-carbon bond formation : from methodology development to bryostatin analogue synthesis.” 2016. Thesis, University of Texas – Austin. Accessed August 23, 2019. http://hdl.handle.net/2152/41729.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

-0166-1890. “Transition metal-catalyzed transfer hydrogenative C-C bond formation : from methodology development to bryostatin analogue synthesis: Transition metal-catalyzed transfer hydrogenative carbon-carbon bond formation : from methodology development to bryostatin analogue synthesis.” 2016. Web. 23 Aug 2019.

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

Vancouver:

-0166-1890. Transition metal-catalyzed transfer hydrogenative C-C bond formation : from methodology development to bryostatin analogue synthesis: Transition metal-catalyzed transfer hydrogenative carbon-carbon bond formation : from methodology development to bryostatin analogue synthesis. [Internet] [Thesis]. University of Texas – Austin; 2016. [cited 2019 Aug 23]. Available from: http://hdl.handle.net/2152/41729.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

-0166-1890. Transition metal-catalyzed transfer hydrogenative C-C bond formation : from methodology development to bryostatin analogue synthesis: Transition metal-catalyzed transfer hydrogenative carbon-carbon bond formation : from methodology development to bryostatin analogue synthesis. [Thesis]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/41729

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation


University of Texas – Austin

18. -5840-9966. Calix[4]pyrrole-based molecular self-assembly.

Degree: 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. (Thesis). 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
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

-5840-9966. “Calix[4]pyrrole-based molecular self-assembly.” 2015. Thesis, University of Texas – Austin. Accessed August 23, 2019. http://hdl.handle.net/2152/46715.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

-5840-9966. “Calix[4]pyrrole-based molecular self-assembly.” 2015. Web. 23 Aug 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] [Thesis]. University of Texas – Austin; 2015. [cited 2019 Aug 23]. 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
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

-5840-9966. Calix[4]pyrrole-based molecular self-assembly. [Thesis]. 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
Not specified: Masters Thesis or Doctoral Dissertation


University of Texas – Austin

19. 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: 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. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/47159

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

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. Thesis, University of Texas – Austin. Accessed August 23, 2019. http://hdl.handle.net/2152/47159.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

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

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

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. [Thesis]. University of Texas – Austin; 2017. Available from: http://hdl.handle.net/2152/47159

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

20. Mitra, Aurpon W. Synthesis of caryolanemagnolol and clovanemagnolol derivatives for molecular pull-down experiments.

Degree: Chemistry, 2011, University of Texas – Austin

 Caryolanemagnolol and clovanemagnolol promote neuronal regeneration in various cell and animal based assays. The protein targets of these natural products are not currently known. Derivatives… (more)

Subjects/Keywords: Caryolanemagnolol; Clovanemagnolol; Affinity chromatography

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APA (6th Edition):

Mitra, A. W. (2011). Synthesis of caryolanemagnolol and clovanemagnolol derivatives for molecular pull-down experiments. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/ETD-UT-2011-12-4680

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Mitra, Aurpon W. “Synthesis of caryolanemagnolol and clovanemagnolol derivatives for molecular pull-down experiments.” 2011. Thesis, University of Texas – Austin. Accessed August 23, 2019. http://hdl.handle.net/2152/ETD-UT-2011-12-4680.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Mitra, Aurpon W. “Synthesis of caryolanemagnolol and clovanemagnolol derivatives for molecular pull-down experiments.” 2011. Web. 23 Aug 2019.

Vancouver:

Mitra AW. Synthesis of caryolanemagnolol and clovanemagnolol derivatives for molecular pull-down experiments. [Internet] [Thesis]. University of Texas – Austin; 2011. [cited 2019 Aug 23]. Available from: http://hdl.handle.net/2152/ETD-UT-2011-12-4680.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Mitra AW. Synthesis of caryolanemagnolol and clovanemagnolol derivatives for molecular pull-down experiments. [Thesis]. University of Texas – Austin; 2011. Available from: http://hdl.handle.net/2152/ETD-UT-2011-12-4680

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

21. Zlotkowski, Katherine Hannah. Chemical biology studies of neuroregenerative small molecules using Caenorhabditis elegans.

Degree: Chemistry, 2015, University of Texas – Austin

 The debilitating effects of spinal cord injury can be attributed to a lack of regeneration in the central nervous system. Identification of growth-promoting pathways, particularly… (more)

Subjects/Keywords: Chemical biology; C. elegans; Small molecules; Spinal cord injury; Regeneration; Clovanemagnolol; Vinaxanthone; Neuronal growth; In vivo assay; Mechanism of action; Laser axotomy; Structure-activity relationship

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APA (6th Edition):

Zlotkowski, K. H. (2015). Chemical biology studies of neuroregenerative small molecules using Caenorhabditis elegans. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/30511

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Zlotkowski, Katherine Hannah. “Chemical biology studies of neuroregenerative small molecules using Caenorhabditis elegans.” 2015. Thesis, University of Texas – Austin. Accessed August 23, 2019. http://hdl.handle.net/2152/30511.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Zlotkowski, Katherine Hannah. “Chemical biology studies of neuroregenerative small molecules using Caenorhabditis elegans.” 2015. Web. 23 Aug 2019.

Vancouver:

Zlotkowski KH. Chemical biology studies of neuroregenerative small molecules using Caenorhabditis elegans. [Internet] [Thesis]. University of Texas – Austin; 2015. [cited 2019 Aug 23]. Available from: http://hdl.handle.net/2152/30511.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Zlotkowski KH. Chemical biology studies of neuroregenerative small molecules using Caenorhabditis elegans. [Thesis]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/30511

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

22. -5628-4490. Transition metal catalyzed regioselective carbon-carbon bond formation mediated by transfer hydrogenation.

Degree: 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. (Thesis). 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
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

-5628-4490. “Transition metal catalyzed regioselective carbon-carbon bond formation mediated by transfer hydrogenation.” 2015. Thesis, University of Texas – Austin. Accessed August 23, 2019. http://hdl.handle.net/2152/30512.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

-5628-4490. “Transition metal catalyzed regioselective carbon-carbon bond formation mediated by transfer hydrogenation.” 2015. Web. 23 Aug 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] [Thesis]. University of Texas – Austin; 2015. [cited 2019 Aug 23]. 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
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

-5628-4490. Transition metal catalyzed regioselective carbon-carbon bond formation mediated by transfer hydrogenation. [Thesis]. 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
Not specified: Masters Thesis or Doctoral Dissertation

23. -6556-6417. Catalytic and polymer composite applications of graphite oxide and the controlled synthesis of donor-acceptor conjugated polymers.

Degree: Chemistry, 2015, University of Texas – Austin

 While much of the recent work regarding carbon materials has centered on monolayer graphene, we have focused on the relatively inexpensive, and readily accessible graphite… (more)

Subjects/Keywords: Graphite oxide; Polymer composites; Conjugated polymers

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APA (6th Edition):

-6556-6417. (2015). Catalytic and polymer composite applications of graphite oxide and the controlled synthesis of donor-acceptor conjugated polymers. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/46545

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

-6556-6417. “Catalytic and polymer composite applications of graphite oxide and the controlled synthesis of donor-acceptor conjugated polymers.” 2015. Thesis, University of Texas – Austin. Accessed August 23, 2019. http://hdl.handle.net/2152/46545.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

-6556-6417. “Catalytic and polymer composite applications of graphite oxide and the controlled synthesis of donor-acceptor conjugated polymers.” 2015. Web. 23 Aug 2019.

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

Vancouver:

-6556-6417. Catalytic and polymer composite applications of graphite oxide and the controlled synthesis of donor-acceptor conjugated polymers. [Internet] [Thesis]. University of Texas – Austin; 2015. [cited 2019 Aug 23]. Available from: http://hdl.handle.net/2152/46545.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

-6556-6417. Catalytic and polymer composite applications of graphite oxide and the controlled synthesis of donor-acceptor conjugated polymers. [Thesis]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/46545

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

.