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You searched for +publisher:"Texas A&M University" +contributor:("Burgess, Kevin"). Showing records 1 – 30 of 46 total matches.

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Texas A&M University

1. Zhou, Qian. The Observation and Study of ELP V5-120 Conformational Changes.

Degree: MS, Chemistry, 2012, Texas A&M University

 Elastin-like polypeptides (ELPs) consist of simple pentapeptide repeats which can be easily modified by substituting various amino acid residues to control its properties. This provides… (more)

Subjects/Keywords: Thermal transition; ELP

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APA (6th Edition):

Zhou, Q. (2012). The Observation and Study of ELP V5-120 Conformational Changes. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/148149

Chicago Manual of Style (16th Edition):

Zhou, Qian. “The Observation and Study of ELP V5-120 Conformational Changes.” 2012. Masters Thesis, Texas A&M University. Accessed December 05, 2020. http://hdl.handle.net/1969.1/148149.

MLA Handbook (7th Edition):

Zhou, Qian. “The Observation and Study of ELP V5-120 Conformational Changes.” 2012. Web. 05 Dec 2020.

Vancouver:

Zhou Q. The Observation and Study of ELP V5-120 Conformational Changes. [Internet] [Masters thesis]. Texas A&M University; 2012. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1969.1/148149.

Council of Science Editors:

Zhou Q. The Observation and Study of ELP V5-120 Conformational Changes. [Masters Thesis]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/148149


Texas A&M University

2. Liu, Zhen. Understanding and Targeting Lipid Metabolism of Mycobacterium tuberculosis.

Degree: PhD, Chemistry, 2013, Texas A&M University

 Mycobacterium tuberculosis (M. tuberculosis) contains a wide array of genes responsible for the synthesis and secretion of a variety of bioactive lipids. The genes represent… (more)

Subjects/Keywords: Structural biology; Enzymology; Drug discovery; Lipid metabolism

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APA (6th Edition):

Liu, Z. (2013). Understanding and Targeting Lipid Metabolism of Mycobacterium tuberculosis. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/151650

Chicago Manual of Style (16th Edition):

Liu, Zhen. “Understanding and Targeting Lipid Metabolism of Mycobacterium tuberculosis.” 2013. Doctoral Dissertation, Texas A&M University. Accessed December 05, 2020. http://hdl.handle.net/1969.1/151650.

MLA Handbook (7th Edition):

Liu, Zhen. “Understanding and Targeting Lipid Metabolism of Mycobacterium tuberculosis.” 2013. Web. 05 Dec 2020.

Vancouver:

Liu Z. Understanding and Targeting Lipid Metabolism of Mycobacterium tuberculosis. [Internet] [Doctoral dissertation]. Texas A&M University; 2013. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1969.1/151650.

Council of Science Editors:

Liu Z. Understanding and Targeting Lipid Metabolism of Mycobacterium tuberculosis. [Doctoral Dissertation]. Texas A&M University; 2013. Available from: http://hdl.handle.net/1969.1/151650


Texas A&M University

3. Kim, Eun Jin. New Strategies in the Localization of Natural Product Biosynthetic Pathways and Achieving Heterologous Expression.

Degree: PhD, Chemistry, 2011, Texas A&M University

 Natural products have long furnished medical science playing a significant role in drug discovery and development. Their importance notwithstanding, it is estimated that less than… (more)

Subjects/Keywords: cDNA library; Fosmid library; Genbetic selection; Heterologous Expression; Riboswitches; Biotin biosynthetic pathway; Natural product

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APA (6th Edition):

Kim, E. J. (2011). New Strategies in the Localization of Natural Product Biosynthetic Pathways and Achieving Heterologous Expression. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7427

Chicago Manual of Style (16th Edition):

Kim, Eun Jin. “New Strategies in the Localization of Natural Product Biosynthetic Pathways and Achieving Heterologous Expression.” 2011. Doctoral Dissertation, Texas A&M University. Accessed December 05, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7427.

MLA Handbook (7th Edition):

Kim, Eun Jin. “New Strategies in the Localization of Natural Product Biosynthetic Pathways and Achieving Heterologous Expression.” 2011. Web. 05 Dec 2020.

Vancouver:

Kim EJ. New Strategies in the Localization of Natural Product Biosynthetic Pathways and Achieving Heterologous Expression. [Internet] [Doctoral dissertation]. Texas A&M University; 2011. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7427.

Council of Science Editors:

Kim EJ. New Strategies in the Localization of Natural Product Biosynthetic Pathways and Achieving Heterologous Expression. [Doctoral Dissertation]. Texas A&M University; 2011. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7427


Texas A&M University

4. Kim, Haelee. Structure-guided Inhibitor Design of Mycobacterium Tuberculosis Drug Targets from Central Carbon Metabolism.

Degree: PhD, Chemistry, 2016, Texas A&M University

 A key determinant of the pathogenicity of M. tuberculosis (Mtb) is its ability to conserve energy and resources by altering its intermediate metabolism response to… (more)

Subjects/Keywords: CCM; PEPCK; TB drug; selective inhibitor; PykA; GTP-competitive inhibitor; X-ray crystallography; Structure-guided inhibitor design; Mycobacterium tuberculosis

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APA (6th Edition):

Kim, H. (2016). Structure-guided Inhibitor Design of Mycobacterium Tuberculosis Drug Targets from Central Carbon Metabolism. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/187362

Chicago Manual of Style (16th Edition):

Kim, Haelee. “Structure-guided Inhibitor Design of Mycobacterium Tuberculosis Drug Targets from Central Carbon Metabolism.” 2016. Doctoral Dissertation, Texas A&M University. Accessed December 05, 2020. http://hdl.handle.net/1969.1/187362.

MLA Handbook (7th Edition):

Kim, Haelee. “Structure-guided Inhibitor Design of Mycobacterium Tuberculosis Drug Targets from Central Carbon Metabolism.” 2016. Web. 05 Dec 2020.

Vancouver:

Kim H. Structure-guided Inhibitor Design of Mycobacterium Tuberculosis Drug Targets from Central Carbon Metabolism. [Internet] [Doctoral dissertation]. Texas A&M University; 2016. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1969.1/187362.

Council of Science Editors:

Kim H. Structure-guided Inhibitor Design of Mycobacterium Tuberculosis Drug Targets from Central Carbon Metabolism. [Doctoral Dissertation]. Texas A&M University; 2016. Available from: http://hdl.handle.net/1969.1/187362


Texas A&M University

5. Wang, Zhipeng. The Chemical Synthetic Investigation of Proteins with Sitespecific Lysine Post-Translational Modifications.

Degree: PhD, Chemistry, 2018, Texas A&M University

 In the recent decade, an increasing amount of protein post-translational modifications (PTMs) have been discovered, which are important epigenetic markers widespread on nucleic and cytoplasmic… (more)

Subjects/Keywords: Protein chemical biology; Post-translational modification; Lysine; noncanonical amino acids

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APA (6th Edition):

Wang, Z. (2018). The Chemical Synthetic Investigation of Proteins with Sitespecific Lysine Post-Translational Modifications. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/173444

Chicago Manual of Style (16th Edition):

Wang, Zhipeng. “The Chemical Synthetic Investigation of Proteins with Sitespecific Lysine Post-Translational Modifications.” 2018. Doctoral Dissertation, Texas A&M University. Accessed December 05, 2020. http://hdl.handle.net/1969.1/173444.

MLA Handbook (7th Edition):

Wang, Zhipeng. “The Chemical Synthetic Investigation of Proteins with Sitespecific Lysine Post-Translational Modifications.” 2018. Web. 05 Dec 2020.

Vancouver:

Wang Z. The Chemical Synthetic Investigation of Proteins with Sitespecific Lysine Post-Translational Modifications. [Internet] [Doctoral dissertation]. Texas A&M University; 2018. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1969.1/173444.

Council of Science Editors:

Wang Z. The Chemical Synthetic Investigation of Proteins with Sitespecific Lysine Post-Translational Modifications. [Doctoral Dissertation]. Texas A&M University; 2018. Available from: http://hdl.handle.net/1969.1/173444


Texas A&M University

6. Han, Junyan. Design, Syntheses and Biological Applications of Through-bond Energy Transfer Cassettes and Novel Non-covalently Cell Penetrating Peptides.

Degree: PhD, Chemistry, 2012, Texas A&M University

 A xanthene-BODIPY cassette is used as a ratiometric intracellular pH reporter for imaging protein-dye conjugates in living cells. A model was hypothesized to explain the… (more)

Subjects/Keywords: energy transfer; cell penetrating peptide; pH probes

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APA (6th Edition):

Han, J. (2012). Design, Syntheses and Biological Applications of Through-bond Energy Transfer Cassettes and Novel Non-covalently Cell Penetrating Peptides. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2009-08-7016

Chicago Manual of Style (16th Edition):

Han, Junyan. “Design, Syntheses and Biological Applications of Through-bond Energy Transfer Cassettes and Novel Non-covalently Cell Penetrating Peptides.” 2012. Doctoral Dissertation, Texas A&M University. Accessed December 05, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2009-08-7016.

MLA Handbook (7th Edition):

Han, Junyan. “Design, Syntheses and Biological Applications of Through-bond Energy Transfer Cassettes and Novel Non-covalently Cell Penetrating Peptides.” 2012. Web. 05 Dec 2020.

Vancouver:

Han J. Design, Syntheses and Biological Applications of Through-bond Energy Transfer Cassettes and Novel Non-covalently Cell Penetrating Peptides. [Internet] [Doctoral dissertation]. Texas A&M University; 2012. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-08-7016.

Council of Science Editors:

Han J. Design, Syntheses and Biological Applications of Through-bond Energy Transfer Cassettes and Novel Non-covalently Cell Penetrating Peptides. [Doctoral Dissertation]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-08-7016


Texas A&M University

7. Xin, Dongyue. Design and Synthesis of Small Molecules to Target Protein-Protein Interactions.

Degree: PhD, Chemistry, 2016, Texas A&M University

 Protein-protein interactions (PPIs) play key regulatory roles in biological systems, and some of these are interesting drug targets. Consequently, it is important to develop generally… (more)

Subjects/Keywords: Protein-Protein Interactions; Interface Mimicry; Conformational Studies; Oligo-Piperidine-Piperidinone; Cyclic Peptides; Antithrombin

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APA (6th Edition):

Xin, D. (2016). Design and Synthesis of Small Molecules to Target Protein-Protein Interactions. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/156879

Chicago Manual of Style (16th Edition):

Xin, Dongyue. “Design and Synthesis of Small Molecules to Target Protein-Protein Interactions.” 2016. Doctoral Dissertation, Texas A&M University. Accessed December 05, 2020. http://hdl.handle.net/1969.1/156879.

MLA Handbook (7th Edition):

Xin, Dongyue. “Design and Synthesis of Small Molecules to Target Protein-Protein Interactions.” 2016. Web. 05 Dec 2020.

Vancouver:

Xin D. Design and Synthesis of Small Molecules to Target Protein-Protein Interactions. [Internet] [Doctoral dissertation]. Texas A&M University; 2016. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1969.1/156879.

Council of Science Editors:

Xin D. Design and Synthesis of Small Molecules to Target Protein-Protein Interactions. [Doctoral Dissertation]. Texas A&M University; 2016. Available from: http://hdl.handle.net/1969.1/156879


Texas A&M University

8. Jung, Hunmin. Development of Potent and Selective Inhibitors of Mycobacterium Tuberculosis, Plasmodium Falciparum and Staphylococcus Aureus Dihydrofolate Reductase.

Degree: PhD, Chemistry, 2014, Texas A&M University

 The goal of this study was to develop drugs that exclusively affect pathogenic dihydrofolate reductase (DHFR) without causing harm to the human counterpart. To achieve… (more)

Subjects/Keywords: Dihydrofolate reductase; tuberculosis; malaria; selective inhibitor

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APA (6th Edition):

Jung, H. (2014). Development of Potent and Selective Inhibitors of Mycobacterium Tuberculosis, Plasmodium Falciparum and Staphylococcus Aureus Dihydrofolate Reductase. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/154132

Chicago Manual of Style (16th Edition):

Jung, Hunmin. “Development of Potent and Selective Inhibitors of Mycobacterium Tuberculosis, Plasmodium Falciparum and Staphylococcus Aureus Dihydrofolate Reductase.” 2014. Doctoral Dissertation, Texas A&M University. Accessed December 05, 2020. http://hdl.handle.net/1969.1/154132.

MLA Handbook (7th Edition):

Jung, Hunmin. “Development of Potent and Selective Inhibitors of Mycobacterium Tuberculosis, Plasmodium Falciparum and Staphylococcus Aureus Dihydrofolate Reductase.” 2014. Web. 05 Dec 2020.

Vancouver:

Jung H. Development of Potent and Selective Inhibitors of Mycobacterium Tuberculosis, Plasmodium Falciparum and Staphylococcus Aureus Dihydrofolate Reductase. [Internet] [Doctoral dissertation]. Texas A&M University; 2014. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1969.1/154132.

Council of Science Editors:

Jung H. Development of Potent and Selective Inhibitors of Mycobacterium Tuberculosis, Plasmodium Falciparum and Staphylococcus Aureus Dihydrofolate Reductase. [Doctoral Dissertation]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/154132


Texas A&M University

9. Shrestha, Ritu 1984-. Multi-functional Bio-synthetic Hybrid Nanostructures for Enhanced Cellular Uptake, Endosomal Escape and Targeted Delivery Toward Diagnostics and Therapeutics.

Degree: PhD, Chemistry, 2012, Texas A&M University

 Applications of nanotechnology in medicine, also known as nanomedicine, is a rapidly growing field as it holds great potential in the development of novel therapeutics… (more)

Subjects/Keywords: siRNA delivery; nanomedicine; endosomal escape; nanoparticles; Polymers

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APA (6th Edition):

Shrestha, R. 1. (2012). Multi-functional Bio-synthetic Hybrid Nanostructures for Enhanced Cellular Uptake, Endosomal Escape and Targeted Delivery Toward Diagnostics and Therapeutics. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/148332

Chicago Manual of Style (16th Edition):

Shrestha, Ritu 1984-. “Multi-functional Bio-synthetic Hybrid Nanostructures for Enhanced Cellular Uptake, Endosomal Escape and Targeted Delivery Toward Diagnostics and Therapeutics.” 2012. Doctoral Dissertation, Texas A&M University. Accessed December 05, 2020. http://hdl.handle.net/1969.1/148332.

MLA Handbook (7th Edition):

Shrestha, Ritu 1984-. “Multi-functional Bio-synthetic Hybrid Nanostructures for Enhanced Cellular Uptake, Endosomal Escape and Targeted Delivery Toward Diagnostics and Therapeutics.” 2012. Web. 05 Dec 2020.

Vancouver:

Shrestha R1. Multi-functional Bio-synthetic Hybrid Nanostructures for Enhanced Cellular Uptake, Endosomal Escape and Targeted Delivery Toward Diagnostics and Therapeutics. [Internet] [Doctoral dissertation]. Texas A&M University; 2012. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1969.1/148332.

Council of Science Editors:

Shrestha R1. Multi-functional Bio-synthetic Hybrid Nanostructures for Enhanced Cellular Uptake, Endosomal Escape and Targeted Delivery Toward Diagnostics and Therapeutics. [Doctoral Dissertation]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/148332


Texas A&M University

10. Ko, Eunhwa. Exploring Key Orientations of Small Molecules to Disrupt Protein-protein Interactions.

Degree: PhD, Chemistry, 2012, Texas A&M University

 Protein-protein interactions (PPIs) are attractive targets because of their therapeutic potential. One approach to design small molecules that can disrupt the PPIs is to use… (more)

Subjects/Keywords: Explores Key Orientation; Universal Peptidomimetics; minimalist mimics; protein-protein interactions; TrkC; targeted drug delivery; triazole-based beta-turn mimics; bivalent mimics

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APA (6th Edition):

Ko, E. (2012). Exploring Key Orientations of Small Molecules to Disrupt Protein-protein Interactions. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2012-05-10961

Chicago Manual of Style (16th Edition):

Ko, Eunhwa. “Exploring Key Orientations of Small Molecules to Disrupt Protein-protein Interactions.” 2012. Doctoral Dissertation, Texas A&M University. Accessed December 05, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2012-05-10961.

MLA Handbook (7th Edition):

Ko, Eunhwa. “Exploring Key Orientations of Small Molecules to Disrupt Protein-protein Interactions.” 2012. Web. 05 Dec 2020.

Vancouver:

Ko E. Exploring Key Orientations of Small Molecules to Disrupt Protein-protein Interactions. [Internet] [Doctoral dissertation]. Texas A&M University; 2012. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2012-05-10961.

Council of Science Editors:

Ko E. Exploring Key Orientations of Small Molecules to Disrupt Protein-protein Interactions. [Doctoral Dissertation]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2012-05-10961


Texas A&M University

11. Lin, Yun. Design and Development of Intricate Nanomedical Devices through Compositional, Dimensional and Structural Control.

Degree: PhD, Chemistry, 2012, Texas A&M University

 Nanomedicine, the medical application of nanotechnology, uses nanoscale objects that exist at the interface between small molecule and the macroscopic world for medical diagnosis and… (more)

Subjects/Keywords: polymer nanoparticles; nanomedicine; drug delivery

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APA (6th Edition):

Lin, Y. (2012). Design and Development of Intricate Nanomedical Devices through Compositional, Dimensional and Structural Control. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2012-05-10923

Chicago Manual of Style (16th Edition):

Lin, Yun. “Design and Development of Intricate Nanomedical Devices through Compositional, Dimensional and Structural Control.” 2012. Doctoral Dissertation, Texas A&M University. Accessed December 05, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2012-05-10923.

MLA Handbook (7th Edition):

Lin, Yun. “Design and Development of Intricate Nanomedical Devices through Compositional, Dimensional and Structural Control.” 2012. Web. 05 Dec 2020.

Vancouver:

Lin Y. Design and Development of Intricate Nanomedical Devices through Compositional, Dimensional and Structural Control. [Internet] [Doctoral dissertation]. Texas A&M University; 2012. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2012-05-10923.

Council of Science Editors:

Lin Y. Design and Development of Intricate Nanomedical Devices through Compositional, Dimensional and Structural Control. [Doctoral Dissertation]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2012-05-10923


Texas A&M University

12. Jose, Jiney. Synthesis of Through-bond Energy Transfer Cassettes and Their Encapsulation in Silica and Calcium Phosphate Nanoparticles.

Degree: PhD, Chemistry, 2011, Texas A&M University

 Water-soluble fluorescent probes with emission in the 600-800 nm region have significant potential in biological applications such as cell imaging. Most fluorescent probes however suffer… (more)

Subjects/Keywords: Fluorescent dyes; nanoparticles

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APA (6th Edition):

Jose, J. (2011). Synthesis of Through-bond Energy Transfer Cassettes and Their Encapsulation in Silica and Calcium Phosphate Nanoparticles. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7334

Chicago Manual of Style (16th Edition):

Jose, Jiney. “Synthesis of Through-bond Energy Transfer Cassettes and Their Encapsulation in Silica and Calcium Phosphate Nanoparticles.” 2011. Doctoral Dissertation, Texas A&M University. Accessed December 05, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7334.

MLA Handbook (7th Edition):

Jose, Jiney. “Synthesis of Through-bond Energy Transfer Cassettes and Their Encapsulation in Silica and Calcium Phosphate Nanoparticles.” 2011. Web. 05 Dec 2020.

Vancouver:

Jose J. Synthesis of Through-bond Energy Transfer Cassettes and Their Encapsulation in Silica and Calcium Phosphate Nanoparticles. [Internet] [Doctoral dissertation]. Texas A&M University; 2011. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7334.

Council of Science Editors:

Jose J. Synthesis of Through-bond Energy Transfer Cassettes and Their Encapsulation in Silica and Calcium Phosphate Nanoparticles. [Doctoral Dissertation]. Texas A&M University; 2011. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7334


Texas A&M University

13. Kamkaew, Anyanee. TrkC Targeted Probes for Cancer Diagnosis and Therapeutics.

Degree: PhD, Chemistry, 2015, Texas A&M University

 This dissertation features a small molecule, non-peptidic, ligand designed to bind a cell surface receptor called tropomyosin receptor kinase C (TrkC). TrkC is overexpressed on… (more)

Subjects/Keywords: TrkC; Theranosis; targeting

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APA (6th Edition):

Kamkaew, A. (2015). TrkC Targeted Probes for Cancer Diagnosis and Therapeutics. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/187448

Chicago Manual of Style (16th Edition):

Kamkaew, Anyanee. “TrkC Targeted Probes for Cancer Diagnosis and Therapeutics.” 2015. Doctoral Dissertation, Texas A&M University. Accessed December 05, 2020. http://hdl.handle.net/1969.1/187448.

MLA Handbook (7th Edition):

Kamkaew, Anyanee. “TrkC Targeted Probes for Cancer Diagnosis and Therapeutics.” 2015. Web. 05 Dec 2020.

Vancouver:

Kamkaew A. TrkC Targeted Probes for Cancer Diagnosis and Therapeutics. [Internet] [Doctoral dissertation]. Texas A&M University; 2015. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1969.1/187448.

Council of Science Editors:

Kamkaew A. TrkC Targeted Probes for Cancer Diagnosis and Therapeutics. [Doctoral Dissertation]. Texas A&M University; 2015. Available from: http://hdl.handle.net/1969.1/187448


Texas A&M University

14. Taechalertpaisarn, Jaru. Design, Optimization and Syntheses of Small Molecules to Disrupt Protein-Protein Interactions.

Degree: PhD, Chemistry, 2018, Texas A&M University

 Protein-protein interactions (PPIs) are one of the basic mechanisms in cellular biology, but also involve in diseases if they are dysregulation. Disrupting aberrant PPI activities… (more)

Subjects/Keywords: Protein-protein Interactions; Small molecules; EKO; PCSK9 protein; Nef protein; NEDD8 protein

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APA (6th Edition):

Taechalertpaisarn, J. (2018). Design, Optimization and Syntheses of Small Molecules to Disrupt Protein-Protein Interactions. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/173323

Chicago Manual of Style (16th Edition):

Taechalertpaisarn, Jaru. “Design, Optimization and Syntheses of Small Molecules to Disrupt Protein-Protein Interactions.” 2018. Doctoral Dissertation, Texas A&M University. Accessed December 05, 2020. http://hdl.handle.net/1969.1/173323.

MLA Handbook (7th Edition):

Taechalertpaisarn, Jaru. “Design, Optimization and Syntheses of Small Molecules to Disrupt Protein-Protein Interactions.” 2018. Web. 05 Dec 2020.

Vancouver:

Taechalertpaisarn J. Design, Optimization and Syntheses of Small Molecules to Disrupt Protein-Protein Interactions. [Internet] [Doctoral dissertation]. Texas A&M University; 2018. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1969.1/173323.

Council of Science Editors:

Taechalertpaisarn J. Design, Optimization and Syntheses of Small Molecules to Disrupt Protein-Protein Interactions. [Doctoral Dissertation]. Texas A&M University; 2018. Available from: http://hdl.handle.net/1969.1/173323

15. Kang, Jun. Chromium-Catalyzed Homoaldol Equivalent Reaction, Indium-Mediated Cycloisomerization, and Palladium-Catalyzed Cross-Coupling Reaction.

Degree: PhD, Chemistry, 2011, Texas A&M University

 The homoaldol reaction is one of the most powerful methods for the construction of C–C bonds as well as 1,4-oxygenated compounds yet this reaction remains… (more)

Subjects/Keywords: homoaldol reaction; Chromium; Cr(III)-Mn(0) redox condition; homoenolates; 1,4-oxygenated compounds; diols; lactols; stereoselective epoxidation; stereoselective cyclopropanation; Furans; indium; acetylenic α,β-epoxides; cycloisomerization; palladium; Cross-coupling reactions; α-alkynyl carbonyl compounds

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APA (6th Edition):

Kang, J. (2011). Chromium-Catalyzed Homoaldol Equivalent Reaction, Indium-Mediated Cycloisomerization, and Palladium-Catalyzed Cross-Coupling Reaction. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2011-08-77

Chicago Manual of Style (16th Edition):

Kang, Jun. “Chromium-Catalyzed Homoaldol Equivalent Reaction, Indium-Mediated Cycloisomerization, and Palladium-Catalyzed Cross-Coupling Reaction.” 2011. Doctoral Dissertation, Texas A&M University. Accessed December 05, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2011-08-77.

MLA Handbook (7th Edition):

Kang, Jun. “Chromium-Catalyzed Homoaldol Equivalent Reaction, Indium-Mediated Cycloisomerization, and Palladium-Catalyzed Cross-Coupling Reaction.” 2011. Web. 05 Dec 2020.

Vancouver:

Kang J. Chromium-Catalyzed Homoaldol Equivalent Reaction, Indium-Mediated Cycloisomerization, and Palladium-Catalyzed Cross-Coupling Reaction. [Internet] [Doctoral dissertation]. Texas A&M University; 2011. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2011-08-77.

Council of Science Editors:

Kang J. Chromium-Catalyzed Homoaldol Equivalent Reaction, Indium-Mediated Cycloisomerization, and Palladium-Catalyzed Cross-Coupling Reaction. [Doctoral Dissertation]. Texas A&M University; 2011. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2011-08-77

16. Thivierge, Cliferson. Design and Syntheses of Dyes for Biological Applications.

Degree: PhD, Chemistry, 2012, Texas A&M University

 The challenges in modern biological imaging applications are two-fold: (i) to develop better methods of imaging, and (ii) develop dyes that are suitable for these… (more)

Subjects/Keywords: Fluorescent Dyes; PDT Agents; BODIPY Dyes

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APA (6th Edition):

Thivierge, C. (2012). Design and Syntheses of Dyes for Biological Applications. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2011-05-9374

Chicago Manual of Style (16th Edition):

Thivierge, Cliferson. “Design and Syntheses of Dyes for Biological Applications.” 2012. Doctoral Dissertation, Texas A&M University. Accessed December 05, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2011-05-9374.

MLA Handbook (7th Edition):

Thivierge, Cliferson. “Design and Syntheses of Dyes for Biological Applications.” 2012. Web. 05 Dec 2020.

Vancouver:

Thivierge C. Design and Syntheses of Dyes for Biological Applications. [Internet] [Doctoral dissertation]. Texas A&M University; 2012. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2011-05-9374.

Council of Science Editors:

Thivierge C. Design and Syntheses of Dyes for Biological Applications. [Doctoral Dissertation]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2011-05-9374

17. Zhu, Ye. Asymmetric Hydrogenations of Chiral Acyclic Alkenes for Important Chiron Syntheses.

Degree: PhD, Chemistry, 2012, Texas A&M University

 Hydrogenation of "largely unfunctionalized" alkenes has been an active area of research for about a decade. Many catalysts have been prepared but we noticed that… (more)

Subjects/Keywords: N,carbene-Iridium; diastereoselective; hydrogenation; alkene; chiron

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APA (6th Edition):

Zhu, Y. (2012). Asymmetric Hydrogenations of Chiral Acyclic Alkenes for Important Chiron Syntheses. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2011-05-9231

Chicago Manual of Style (16th Edition):

Zhu, Ye. “Asymmetric Hydrogenations of Chiral Acyclic Alkenes for Important Chiron Syntheses.” 2012. Doctoral Dissertation, Texas A&M University. Accessed December 05, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2011-05-9231.

MLA Handbook (7th Edition):

Zhu, Ye. “Asymmetric Hydrogenations of Chiral Acyclic Alkenes for Important Chiron Syntheses.” 2012. Web. 05 Dec 2020.

Vancouver:

Zhu Y. Asymmetric Hydrogenations of Chiral Acyclic Alkenes for Important Chiron Syntheses. [Internet] [Doctoral dissertation]. Texas A&M University; 2012. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2011-05-9231.

Council of Science Editors:

Zhu Y. Asymmetric Hydrogenations of Chiral Acyclic Alkenes for Important Chiron Syntheses. [Doctoral Dissertation]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2011-05-9231

18. Zhou, Hua. Synthesis and Application of Useful Organic Building Blocks and Cyclic Tetrapeptide.

Degree: MS, Chemistry, 2014, Texas A&M University

 Drug designing usually encounters two major difficulties: construction of small molecules and target finding for the molecules. This is frustrating because either one requires tremendous… (more)

Subjects/Keywords: cyclic tetrapeptide; conformational analysis; vinyl; homo-Roche ester; asymmetric hydrogenation; organocatalysis

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APA (6th Edition):

Zhou, H. (2014). Synthesis and Application of Useful Organic Building Blocks and Cyclic Tetrapeptide. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/154016

Chicago Manual of Style (16th Edition):

Zhou, Hua. “Synthesis and Application of Useful Organic Building Blocks and Cyclic Tetrapeptide.” 2014. Masters Thesis, Texas A&M University. Accessed December 05, 2020. http://hdl.handle.net/1969.1/154016.

MLA Handbook (7th Edition):

Zhou, Hua. “Synthesis and Application of Useful Organic Building Blocks and Cyclic Tetrapeptide.” 2014. Web. 05 Dec 2020.

Vancouver:

Zhou H. Synthesis and Application of Useful Organic Building Blocks and Cyclic Tetrapeptide. [Internet] [Masters thesis]. Texas A&M University; 2014. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1969.1/154016.

Council of Science Editors:

Zhou H. Synthesis and Application of Useful Organic Building Blocks and Cyclic Tetrapeptide. [Masters Thesis]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/154016

19. Khumsubdee, Sakunchai. Synthesis and Application of New Ligands Derived from N-Heterocyclic Carbenes, Phosphines and Phosphites for Asymmetric Hydrogenations.

Degree: PhD, Chemistry, 2013, Texas A&M University

 N-Heterocyclic carbene and phosphorus ligands have been synthesized and used for many catalytic reactions including chiral analogs of Crabtree’s catalyst for asymmetric hydrogenation. These catalysts… (more)

Subjects/Keywords: Asymmetric Hydrogenation; carbenes; iridium

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APA (6th Edition):

Khumsubdee, S. (2013). Synthesis and Application of New Ligands Derived from N-Heterocyclic Carbenes, Phosphines and Phosphites for Asymmetric Hydrogenations. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/151725

Chicago Manual of Style (16th Edition):

Khumsubdee, Sakunchai. “Synthesis and Application of New Ligands Derived from N-Heterocyclic Carbenes, Phosphines and Phosphites for Asymmetric Hydrogenations.” 2013. Doctoral Dissertation, Texas A&M University. Accessed December 05, 2020. http://hdl.handle.net/1969.1/151725.

MLA Handbook (7th Edition):

Khumsubdee, Sakunchai. “Synthesis and Application of New Ligands Derived from N-Heterocyclic Carbenes, Phosphines and Phosphites for Asymmetric Hydrogenations.” 2013. Web. 05 Dec 2020.

Vancouver:

Khumsubdee S. Synthesis and Application of New Ligands Derived from N-Heterocyclic Carbenes, Phosphines and Phosphites for Asymmetric Hydrogenations. [Internet] [Doctoral dissertation]. Texas A&M University; 2013. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1969.1/151725.

Council of Science Editors:

Khumsubdee S. Synthesis and Application of New Ligands Derived from N-Heterocyclic Carbenes, Phosphines and Phosphites for Asymmetric Hydrogenations. [Doctoral Dissertation]. Texas A&M University; 2013. Available from: http://hdl.handle.net/1969.1/151725

20. Reyes, Samuel Onofre J. Expanding beta-turn analogs for mimicking protein-protein hot spots.

Degree: PhD, Chemistry, 2009, Texas A&M University

 Solid-phase syntheses of two 14-membered ring peptidomimetics were done to determine whether or not a beta-turn structure can facilitate macrocyclization. NMR methods, together with CD… (more)

Subjects/Keywords: peptidomimetics; solid-phase synthesis; solution phase synthesis; medicinal chemistry

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APA (6th Edition):

Reyes, S. O. J. (2009). Expanding beta-turn analogs for mimicking protein-protein hot spots. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-1748

Chicago Manual of Style (16th Edition):

Reyes, Samuel Onofre J. “Expanding beta-turn analogs for mimicking protein-protein hot spots.” 2009. Doctoral Dissertation, Texas A&M University. Accessed December 05, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-1748.

MLA Handbook (7th Edition):

Reyes, Samuel Onofre J. “Expanding beta-turn analogs for mimicking protein-protein hot spots.” 2009. Web. 05 Dec 2020.

Vancouver:

Reyes SOJ. Expanding beta-turn analogs for mimicking protein-protein hot spots. [Internet] [Doctoral dissertation]. Texas A&M University; 2009. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-1748.

Council of Science Editors:

Reyes SOJ. Expanding beta-turn analogs for mimicking protein-protein hot spots. [Doctoral Dissertation]. Texas A&M University; 2009. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-1748

21. Angell, Yu Li. Triazole based peptidomimetics for mimicking protein-protein hot spots.

Degree: PhD, Chemistry, 2009, Texas A&M University

 Copper-mediated alkyne-azide cycloadditions yield 1,4-disubstituted triazoles with high chemoselectivity that can be used in many ways. For instance, when alkyne or azido peptide units combine… (more)

Subjects/Keywords: Triazole; peptidomimetics

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APA (6th Edition):

Angell, Y. L. (2009). Triazole based peptidomimetics for mimicking protein-protein hot spots. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-1432

Chicago Manual of Style (16th Edition):

Angell, Yu Li. “Triazole based peptidomimetics for mimicking protein-protein hot spots.” 2009. Doctoral Dissertation, Texas A&M University. Accessed December 05, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-1432.

MLA Handbook (7th Edition):

Angell, Yu Li. “Triazole based peptidomimetics for mimicking protein-protein hot spots.” 2009. Web. 05 Dec 2020.

Vancouver:

Angell YL. Triazole based peptidomimetics for mimicking protein-protein hot spots. [Internet] [Doctoral dissertation]. Texas A&M University; 2009. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-1432.

Council of Science Editors:

Angell YL. Triazole based peptidomimetics for mimicking protein-protein hot spots. [Doctoral Dissertation]. Texas A&M University; 2009. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-1432

22. He, Xun. Development of Stimuli-responsive Polypeptide-based Gelators for Bioapplications and Photo-patterning Technologies.

Degree: PhD, Chemistry, 2017, Texas A&M University

 The past decade has witnessed significantly increased interest in the development of smart polypeptide based organo- and hydrogel systems with stimuli responsiveness, especially those that… (more)

Subjects/Keywords: Polypeptide; hydrogel; assembly; stimuli; sol-gel transition

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APA (6th Edition):

He, X. (2017). Development of Stimuli-responsive Polypeptide-based Gelators for Bioapplications and Photo-patterning Technologies. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/161429

Chicago Manual of Style (16th Edition):

He, Xun. “Development of Stimuli-responsive Polypeptide-based Gelators for Bioapplications and Photo-patterning Technologies.” 2017. Doctoral Dissertation, Texas A&M University. Accessed December 05, 2020. http://hdl.handle.net/1969.1/161429.

MLA Handbook (7th Edition):

He, Xun. “Development of Stimuli-responsive Polypeptide-based Gelators for Bioapplications and Photo-patterning Technologies.” 2017. Web. 05 Dec 2020.

Vancouver:

He X. Development of Stimuli-responsive Polypeptide-based Gelators for Bioapplications and Photo-patterning Technologies. [Internet] [Doctoral dissertation]. Texas A&M University; 2017. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1969.1/161429.

Council of Science Editors:

He X. Development of Stimuli-responsive Polypeptide-based Gelators for Bioapplications and Photo-patterning Technologies. [Doctoral Dissertation]. Texas A&M University; 2017. Available from: http://hdl.handle.net/1969.1/161429

23. Demott, Jessica Carman. Unsaturated Pt Pincer Complexes and Attempts toward the Isolation of a Methane σ-Complex.

Degree: PhD, Chemistry, 2015, Texas A&M University

 Alkane σ-complexes have been identified as key intermediates in C-H bond activation and subsequent functionalization of alkanes. Methane and larger saturated alkanes, however, are sterically… (more)

Subjects/Keywords: PNP pincer ligand; oxidative addition; alkane complexes; coordination; platinum(II); metal-complexes; C-H activation

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APA (6th Edition):

Demott, J. C. (2015). Unsaturated Pt Pincer Complexes and Attempts toward the Isolation of a Methane σ-Complex. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/156372

Chicago Manual of Style (16th Edition):

Demott, Jessica Carman. “Unsaturated Pt Pincer Complexes and Attempts toward the Isolation of a Methane σ-Complex.” 2015. Doctoral Dissertation, Texas A&M University. Accessed December 05, 2020. http://hdl.handle.net/1969.1/156372.

MLA Handbook (7th Edition):

Demott, Jessica Carman. “Unsaturated Pt Pincer Complexes and Attempts toward the Isolation of a Methane σ-Complex.” 2015. Web. 05 Dec 2020.

Vancouver:

Demott JC. Unsaturated Pt Pincer Complexes and Attempts toward the Isolation of a Methane σ-Complex. [Internet] [Doctoral dissertation]. Texas A&M University; 2015. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1969.1/156372.

Council of Science Editors:

Demott JC. Unsaturated Pt Pincer Complexes and Attempts toward the Isolation of a Methane σ-Complex. [Doctoral Dissertation]. Texas A&M University; 2015. Available from: http://hdl.handle.net/1969.1/156372

24. Wang, Shaohui. Synthetic studies toward palau򡭩ne and enantioselective total synthesis of biogenetically related (+)-phakellin and (+)-monobromophakellin.

Degree: PhD, Chemistry, 2009, Texas A&M University

 Oroidin alkaloids, also known as pyrrole-imidazole alkaloids, have become a hot area of chemical and biological research due to their diverse and intriguing structural features… (more)

Subjects/Keywords: alkaloid; palau'amine; phakellin; synthesis

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APA (6th Edition):

Wang, S. (2009). Synthetic studies toward palau򡭩ne and enantioselective total synthesis of biogenetically related (+)-phakellin and (+)-monobromophakellin. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2680

Chicago Manual of Style (16th Edition):

Wang, Shaohui. “Synthetic studies toward palau򡭩ne and enantioselective total synthesis of biogenetically related (+)-phakellin and (+)-monobromophakellin.” 2009. Doctoral Dissertation, Texas A&M University. Accessed December 05, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2680.

MLA Handbook (7th Edition):

Wang, Shaohui. “Synthetic studies toward palau򡭩ne and enantioselective total synthesis of biogenetically related (+)-phakellin and (+)-monobromophakellin.” 2009. Web. 05 Dec 2020.

Vancouver:

Wang S. Synthetic studies toward palau򡭩ne and enantioselective total synthesis of biogenetically related (+)-phakellin and (+)-monobromophakellin. [Internet] [Doctoral dissertation]. Texas A&M University; 2009. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2680.

Council of Science Editors:

Wang S. Synthetic studies toward palau򡭩ne and enantioselective total synthesis of biogenetically related (+)-phakellin and (+)-monobromophakellin. [Doctoral Dissertation]. Texas A&M University; 2009. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2680

25. Steffensen, Mackay Bagley. Methods for the syntheses of compositionally diverse dendrimers.

Degree: PhD, Chemistry, 2005, Texas A&M University

 Dendrimers are a unique class of macromolecules that present perfect branching on a molecular scale. The pattern of branching at the atomic scale is compared… (more)

Subjects/Keywords: Dendrimer; synthesis; multifunctional; chemoselective; triazine; polymer chemistry

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APA (6th Edition):

Steffensen, M. B. (2005). Methods for the syntheses of compositionally diverse dendrimers. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/2724

Chicago Manual of Style (16th Edition):

Steffensen, Mackay Bagley. “Methods for the syntheses of compositionally diverse dendrimers.” 2005. Doctoral Dissertation, Texas A&M University. Accessed December 05, 2020. http://hdl.handle.net/1969.1/2724.

MLA Handbook (7th Edition):

Steffensen, Mackay Bagley. “Methods for the syntheses of compositionally diverse dendrimers.” 2005. Web. 05 Dec 2020.

Vancouver:

Steffensen MB. Methods for the syntheses of compositionally diverse dendrimers. [Internet] [Doctoral dissertation]. Texas A&M University; 2005. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1969.1/2724.

Council of Science Editors:

Steffensen MB. Methods for the syntheses of compositionally diverse dendrimers. [Doctoral Dissertation]. Texas A&M University; 2005. Available from: http://hdl.handle.net/1969.1/2724

26. Green, Kayla Nalynn. Immobilized metallodithiolate ligand supports for construction of bioinorganic model complexes.

Degree: PhD, Chemistry, 2009, Texas A&M University

 The A-cluster active site in acetyl coA synthase exploits a Ni(CGC)2- metallopeptide as a bidentate ligand to chelate the catalytically active square-planar nickel center used… (more)

Subjects/Keywords: Heterogeneous; immobilized; Ni; Fe; Cu; Enzymes; bioinorganic

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APA (6th Edition):

Green, K. N. (2009). Immobilized metallodithiolate ligand supports for construction of bioinorganic model complexes. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2445

Chicago Manual of Style (16th Edition):

Green, Kayla Nalynn. “Immobilized metallodithiolate ligand supports for construction of bioinorganic model complexes.” 2009. Doctoral Dissertation, Texas A&M University. Accessed December 05, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2445.

MLA Handbook (7th Edition):

Green, Kayla Nalynn. “Immobilized metallodithiolate ligand supports for construction of bioinorganic model complexes.” 2009. Web. 05 Dec 2020.

Vancouver:

Green KN. Immobilized metallodithiolate ligand supports for construction of bioinorganic model complexes. [Internet] [Doctoral dissertation]. Texas A&M University; 2009. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2445.

Council of Science Editors:

Green KN. Immobilized metallodithiolate ligand supports for construction of bioinorganic model complexes. [Doctoral Dissertation]. Texas A&M University; 2009. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2445

27. Liu, Jing. Heterocyclic small molecule peptidomimetics.

Degree: PhD, Chemistry, 2009, Texas A&M University

 Polymer-supported synthesis of a close analog (i.e. A) of an early lead, a 14- membered ring peptidomimetic D3, was described. The monovalent molecule was attached… (more)

Subjects/Keywords: Heterocyclic; Peptidomimetics

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APA (6th Edition):

Liu, J. (2009). Heterocyclic small molecule peptidomimetics. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-3125

Chicago Manual of Style (16th Edition):

Liu, Jing. “Heterocyclic small molecule peptidomimetics.” 2009. Doctoral Dissertation, Texas A&M University. Accessed December 05, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-3125.

MLA Handbook (7th Edition):

Liu, Jing. “Heterocyclic small molecule peptidomimetics.” 2009. Web. 05 Dec 2020.

Vancouver:

Liu J. Heterocyclic small molecule peptidomimetics. [Internet] [Doctoral dissertation]. Texas A&M University; 2009. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-3125.

Council of Science Editors:

Liu J. Heterocyclic small molecule peptidomimetics. [Doctoral Dissertation]. Texas A&M University; 2009. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-3125

28. Ogle, James William. N-heterocyclic carbene catalysis: expansion of.

Degree: PhD, Chemistry, 2009, Texas A&M University

 Asymmetric hydrogenation as a general route to polypropionates has been explored for allylic alcohols, acids, and derivatives, which has led to the generation of 2,4-dimethylated… (more)

Subjects/Keywords: catalysis; carbenes; imidazolium; iridium; hydrogenation; asymmetric; electronic

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APA (6th Edition):

Ogle, J. W. (2009). N-heterocyclic carbene catalysis: expansion of. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-3126

Chicago Manual of Style (16th Edition):

Ogle, James William. “N-heterocyclic carbene catalysis: expansion of.” 2009. Doctoral Dissertation, Texas A&M University. Accessed December 05, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-3126.

MLA Handbook (7th Edition):

Ogle, James William. “N-heterocyclic carbene catalysis: expansion of.” 2009. Web. 05 Dec 2020.

Vancouver:

Ogle JW. N-heterocyclic carbene catalysis: expansion of. [Internet] [Doctoral dissertation]. Texas A&M University; 2009. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-3126.

Council of Science Editors:

Ogle JW. N-heterocyclic carbene catalysis: expansion of. [Doctoral Dissertation]. Texas A&M University; 2009. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-3126

29. Estrada, Roy Tonacao, III. Fluorescent Labeling Reagents Optimized for Capillary Electrophoretic Separations.

Degree: PhD, Chemistry, 2012, Texas A&M University

 Fluorescent labeling can improve the detection sensitivity in capillary electrophoretic (CE) separations down to attomolar concentrations. However, most fluorescent labels are not compatible with CE… (more)

Subjects/Keywords: capillary electrophoresis; liquid chromatography; fluorescence labeling; fluorophore; solid phase reagent; acid-cleavable tether; proteins; acridine; pyrene

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APA (6th Edition):

Estrada, Roy Tonacao, I. (2012). Fluorescent Labeling Reagents Optimized for Capillary Electrophoretic Separations. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2010-05-7929

Chicago Manual of Style (16th Edition):

Estrada, Roy Tonacao, III. “Fluorescent Labeling Reagents Optimized for Capillary Electrophoretic Separations.” 2012. Doctoral Dissertation, Texas A&M University. Accessed December 05, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2010-05-7929.

MLA Handbook (7th Edition):

Estrada, Roy Tonacao, III. “Fluorescent Labeling Reagents Optimized for Capillary Electrophoretic Separations.” 2012. Web. 05 Dec 2020.

Vancouver:

Estrada, Roy Tonacao I. Fluorescent Labeling Reagents Optimized for Capillary Electrophoretic Separations. [Internet] [Doctoral dissertation]. Texas A&M University; 2012. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-05-7929.

Council of Science Editors:

Estrada, Roy Tonacao I. Fluorescent Labeling Reagents Optimized for Capillary Electrophoretic Separations. [Doctoral Dissertation]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-05-7929


Texas A&M University

30. Li, Lingling. Water-soluble bodipys: syntheses, derivatization and photophysical studies.

Degree: MS, Chemistry, 2009, Texas A&M University

 A set of water-soluble 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) derivatives, has been prepared and their spectroscopic properties examined. These dyes can be used as either donor or acceptor… (more)

Subjects/Keywords: water-soluble; BODIPY

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APA (6th Edition):

Li, L. (2009). Water-soluble bodipys: syntheses, derivatization and photophysical studies. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2448

Chicago Manual of Style (16th Edition):

Li, Lingling. “Water-soluble bodipys: syntheses, derivatization and photophysical studies.” 2009. Masters Thesis, Texas A&M University. Accessed December 05, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2448.

MLA Handbook (7th Edition):

Li, Lingling. “Water-soluble bodipys: syntheses, derivatization and photophysical studies.” 2009. Web. 05 Dec 2020.

Vancouver:

Li L. Water-soluble bodipys: syntheses, derivatization and photophysical studies. [Internet] [Masters thesis]. Texas A&M University; 2009. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2448.

Council of Science Editors:

Li L. Water-soluble bodipys: syntheses, derivatization and photophysical studies. [Masters Thesis]. Texas A&M University; 2009. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2448

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