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You searched for +publisher:"Florida International University" +contributor:("Kathleen S. Rein"). Showing records 1 – 5 of 5 total matches.

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Florida International University

1. Di, Mingping. Syntheses of aza analogs of kainoids.

Degree: PhD, Chemistry, 2006, Florida International University

  The kainoids are a class of non-proteinogenic pyrrolidine dicarboxylates that exhibit both excitatory and excitotoxic activities. These activities are a result of the ability… (more)

Subjects/Keywords: Chemistry

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APA (6th Edition):

Di, M. (2006). Syntheses of aza analogs of kainoids. (Doctoral Dissertation). Florida International University. Retrieved from https://digitalcommons.fiu.edu/etd/2795 ; 10.25148/etd.FI14062265 ; FI14062265

Chicago Manual of Style (16th Edition):

Di, Mingping. “Syntheses of aza analogs of kainoids.” 2006. Doctoral Dissertation, Florida International University. Accessed April 15, 2021. https://digitalcommons.fiu.edu/etd/2795 ; 10.25148/etd.FI14062265 ; FI14062265.

MLA Handbook (7th Edition):

Di, Mingping. “Syntheses of aza analogs of kainoids.” 2006. Web. 15 Apr 2021.

Vancouver:

Di M. Syntheses of aza analogs of kainoids. [Internet] [Doctoral dissertation]. Florida International University; 2006. [cited 2021 Apr 15]. Available from: https://digitalcommons.fiu.edu/etd/2795 ; 10.25148/etd.FI14062265 ; FI14062265.

Council of Science Editors:

Di M. Syntheses of aza analogs of kainoids. [Doctoral Dissertation]. Florida International University; 2006. Available from: https://digitalcommons.fiu.edu/etd/2795 ; 10.25148/etd.FI14062265 ; FI14062265


Florida International University

2. Liu, Li. Absolute Configuration and Biosynthesis of Pahayokolide A from Lyngbya sp. Strain 15-2 of the Florida Everglades.

Degree: Chemistry, 2009, Florida International University

  Pahayokolides A-D are cytotoxic cyclic polypeptides produced by the freshwater cyanobacterium Lyngbya sp. strain 15-2 that possess an unusual β-amino acid, 3-amino-2,5,7,8-tetrahydroxy-10-methylundecanoic acid (Athmu).… (more)

Subjects/Keywords: Lyngbya; Peptide; Pahayokolide A; Absolute configuration; Biosynthesis; NRPS; Stable isotope incprporation; Analytical Chemistry; Biochemistry; Medicinal-Pharmaceutical Chemistry

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APA (6th Edition):

Liu, L. (2009). Absolute Configuration and Biosynthesis of Pahayokolide A from Lyngbya sp. Strain 15-2 of the Florida Everglades. (Thesis). Florida International University. Retrieved from https://digitalcommons.fiu.edu/etd/134 ; 10.25148/etd.FI09120808 ; FI09120808

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, Li. “Absolute Configuration and Biosynthesis of Pahayokolide A from Lyngbya sp. Strain 15-2 of the Florida Everglades.” 2009. Thesis, Florida International University. Accessed April 15, 2021. https://digitalcommons.fiu.edu/etd/134 ; 10.25148/etd.FI09120808 ; FI09120808.

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

MLA Handbook (7th Edition):

Liu, Li. “Absolute Configuration and Biosynthesis of Pahayokolide A from Lyngbya sp. Strain 15-2 of the Florida Everglades.” 2009. Web. 15 Apr 2021.

Vancouver:

Liu L. Absolute Configuration and Biosynthesis of Pahayokolide A from Lyngbya sp. Strain 15-2 of the Florida Everglades. [Internet] [Thesis]. Florida International University; 2009. [cited 2021 Apr 15]. Available from: https://digitalcommons.fiu.edu/etd/134 ; 10.25148/etd.FI09120808 ; FI09120808.

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

Council of Science Editors:

Liu L. Absolute Configuration and Biosynthesis of Pahayokolide A from Lyngbya sp. Strain 15-2 of the Florida Everglades. [Thesis]. Florida International University; 2009. Available from: https://digitalcommons.fiu.edu/etd/134 ; 10.25148/etd.FI09120808 ; FI09120808

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


Florida International University

3. Rayala, Ramanjaneyulu. Design and Synthesis of Novel Nucleoside Analogues: Oxidative and Reductive Approaches toward Synthesis of 2'-Fluoro Pyrimidine Nucleosides.

Degree: PhD, Chemistry, 2015, Florida International University

  Fluorinated nucleosides, especially the analogues with fluorine atom(s) in the ribose ring, have been known to exert potent biological activities. The first part of… (more)

Subjects/Keywords: Fluorination; Desulfurization; Desulfonylation; Pyrimidines; Purines; 7-Deazapurines; DBH; Click Chemistry; C-H Functionalization; One Electron Oxidation; Carbohydrates; Heterocyclic Compounds; Nucleic Acids, Nucleotides, and Nucleosides

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APA (6th Edition):

Rayala, R. (2015). Design and Synthesis of Novel Nucleoside Analogues: Oxidative and Reductive Approaches toward Synthesis of 2'-Fluoro Pyrimidine Nucleosides. (Doctoral Dissertation). Florida International University. Retrieved from https://digitalcommons.fiu.edu/etd/2172 ; 10.25148/etd.FIDC000129 ; FIDC000129

Chicago Manual of Style (16th Edition):

Rayala, Ramanjaneyulu. “Design and Synthesis of Novel Nucleoside Analogues: Oxidative and Reductive Approaches toward Synthesis of 2'-Fluoro Pyrimidine Nucleosides.” 2015. Doctoral Dissertation, Florida International University. Accessed April 15, 2021. https://digitalcommons.fiu.edu/etd/2172 ; 10.25148/etd.FIDC000129 ; FIDC000129.

MLA Handbook (7th Edition):

Rayala, Ramanjaneyulu. “Design and Synthesis of Novel Nucleoside Analogues: Oxidative and Reductive Approaches toward Synthesis of 2'-Fluoro Pyrimidine Nucleosides.” 2015. Web. 15 Apr 2021.

Vancouver:

Rayala R. Design and Synthesis of Novel Nucleoside Analogues: Oxidative and Reductive Approaches toward Synthesis of 2'-Fluoro Pyrimidine Nucleosides. [Internet] [Doctoral dissertation]. Florida International University; 2015. [cited 2021 Apr 15]. Available from: https://digitalcommons.fiu.edu/etd/2172 ; 10.25148/etd.FIDC000129 ; FIDC000129.

Council of Science Editors:

Rayala R. Design and Synthesis of Novel Nucleoside Analogues: Oxidative and Reductive Approaches toward Synthesis of 2'-Fluoro Pyrimidine Nucleosides. [Doctoral Dissertation]. Florida International University; 2015. Available from: https://digitalcommons.fiu.edu/etd/2172 ; 10.25148/etd.FIDC000129 ; FIDC000129

4. sun, pengfei. Characterization of an Epoxide Hydrolase from the Florida Red Tide Dinoflagellate, Karenia brevis.

Degree: PhD, Chemistry, 2015, Florida International University

  Polyether compounds are a subgroup of natural products with regular occurrence of multiple C-O-C motifs. The biosynthetic origin of polycylic polethers has been studied… (more)

Subjects/Keywords: Karenia brevis; dinoflagellate; brevetoxin; epoxide hydrolase; Biochemistry; Molecular Biology

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APA (6th Edition):

sun, p. (2015). Characterization of an Epoxide Hydrolase from the Florida Red Tide Dinoflagellate, Karenia brevis. (Doctoral Dissertation). Florida International University. Retrieved from https://digitalcommons.fiu.edu/etd/2066 ; 10.25148/etd.FIDC000133 ; FIDC000133

Chicago Manual of Style (16th Edition):

sun, pengfei. “Characterization of an Epoxide Hydrolase from the Florida Red Tide Dinoflagellate, Karenia brevis.” 2015. Doctoral Dissertation, Florida International University. Accessed April 15, 2021. https://digitalcommons.fiu.edu/etd/2066 ; 10.25148/etd.FIDC000133 ; FIDC000133.

MLA Handbook (7th Edition):

sun, pengfei. “Characterization of an Epoxide Hydrolase from the Florida Red Tide Dinoflagellate, Karenia brevis.” 2015. Web. 15 Apr 2021.

Vancouver:

sun p. Characterization of an Epoxide Hydrolase from the Florida Red Tide Dinoflagellate, Karenia brevis. [Internet] [Doctoral dissertation]. Florida International University; 2015. [cited 2021 Apr 15]. Available from: https://digitalcommons.fiu.edu/etd/2066 ; 10.25148/etd.FIDC000133 ; FIDC000133.

Council of Science Editors:

sun p. Characterization of an Epoxide Hydrolase from the Florida Red Tide Dinoflagellate, Karenia brevis. [Doctoral Dissertation]. Florida International University; 2015. Available from: https://digitalcommons.fiu.edu/etd/2066 ; 10.25148/etd.FIDC000133 ; FIDC000133

5. Wang, Wentian. Asymmetric Syntheses of Analogs of Kainic Acid.

Degree: PhD, Chemistry, 2012, Florida International University

  Kainic acid has been used for nearly 50 years as a tool in neuroscience due to its pronounced neuroexcitatory properties. However, the significant price… (more)

Subjects/Keywords: Kainic Acid; Pyrrolidine; Dipolar cycloaddition; Asymmetric; Exo/Endo; Isoxazolidine; Mosher method

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Wang, W. (2012). Asymmetric Syntheses of Analogs of Kainic Acid. (Doctoral Dissertation). Florida International University. Retrieved from https://digitalcommons.fiu.edu/etd/756 ; 10.25148/etd.FI12113007 ; FI12113007

Chicago Manual of Style (16th Edition):

Wang, Wentian. “Asymmetric Syntheses of Analogs of Kainic Acid.” 2012. Doctoral Dissertation, Florida International University. Accessed April 15, 2021. https://digitalcommons.fiu.edu/etd/756 ; 10.25148/etd.FI12113007 ; FI12113007.

MLA Handbook (7th Edition):

Wang, Wentian. “Asymmetric Syntheses of Analogs of Kainic Acid.” 2012. Web. 15 Apr 2021.

Vancouver:

Wang W. Asymmetric Syntheses of Analogs of Kainic Acid. [Internet] [Doctoral dissertation]. Florida International University; 2012. [cited 2021 Apr 15]. Available from: https://digitalcommons.fiu.edu/etd/756 ; 10.25148/etd.FI12113007 ; FI12113007.

Council of Science Editors:

Wang W. Asymmetric Syntheses of Analogs of Kainic Acid. [Doctoral Dissertation]. Florida International University; 2012. Available from: https://digitalcommons.fiu.edu/etd/756 ; 10.25148/etd.FI12113007 ; FI12113007

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