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You searched for subject:(Azetidines). Showing records 1 – 10 of 10 total matches.

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University of Alberta

1. Bott, Tina Marie. The construction of diverse nitrogen-containing heterocycles via the reaction of amines of azides with metallocarbenes.

Degree: PhD, Department of Chemistry, 2012, University of Alberta

 A fundamental goal in organic chemistry is the development of new and innovative ways of transforming simple building blocks into complex structures. The formation of… (more)

Subjects/Keywords: heterocycles; azetidines; azides; Stevens

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APA (6th Edition):

Bott, T. M. (2012). The construction of diverse nitrogen-containing heterocycles via the reaction of amines of azides with metallocarbenes. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/zc77sr37k

Chicago Manual of Style (16th Edition):

Bott, Tina Marie. “The construction of diverse nitrogen-containing heterocycles via the reaction of amines of azides with metallocarbenes.” 2012. Doctoral Dissertation, University of Alberta. Accessed December 03, 2020. https://era.library.ualberta.ca/files/zc77sr37k.

MLA Handbook (7th Edition):

Bott, Tina Marie. “The construction of diverse nitrogen-containing heterocycles via the reaction of amines of azides with metallocarbenes.” 2012. Web. 03 Dec 2020.

Vancouver:

Bott TM. The construction of diverse nitrogen-containing heterocycles via the reaction of amines of azides with metallocarbenes. [Internet] [Doctoral dissertation]. University of Alberta; 2012. [cited 2020 Dec 03]. Available from: https://era.library.ualberta.ca/files/zc77sr37k.

Council of Science Editors:

Bott TM. The construction of diverse nitrogen-containing heterocycles via the reaction of amines of azides with metallocarbenes. [Doctoral Dissertation]. University of Alberta; 2012. Available from: https://era.library.ualberta.ca/files/zc77sr37k


Vanderbilt University

2. O'Reilly, Matthew Charles. Application of Organocatalysis to the Synthesis of Chiral Morpholines, Piperazines, Aziridines, Azetidines, beta-fluoroamines, and gamma-fluoroamines; Discovery of Selective Phospholipase D Inhibitors with Optimized in vivo Properties.

Degree: PhD, Chemistry, 2014, Vanderbilt University

 My doctoral research has focused on (i) using organocatalysis to prepare enantioenriched pharmaceutically relevant scaffolds and (ii) preparing isoenzyme selective inhibitors of phospholipase D. (i)… (more)

Subjects/Keywords: piperazines; morpholines; Phospholipase D; organocatalysis; fluoroamines; aziridines; azetidines

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APA (6th Edition):

O'Reilly, M. C. (2014). Application of Organocatalysis to the Synthesis of Chiral Morpholines, Piperazines, Aziridines, Azetidines, beta-fluoroamines, and gamma-fluoroamines; Discovery of Selective Phospholipase D Inhibitors with Optimized in vivo Properties. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/12701

Chicago Manual of Style (16th Edition):

O'Reilly, Matthew Charles. “Application of Organocatalysis to the Synthesis of Chiral Morpholines, Piperazines, Aziridines, Azetidines, beta-fluoroamines, and gamma-fluoroamines; Discovery of Selective Phospholipase D Inhibitors with Optimized in vivo Properties.” 2014. Doctoral Dissertation, Vanderbilt University. Accessed December 03, 2020. http://hdl.handle.net/1803/12701.

MLA Handbook (7th Edition):

O'Reilly, Matthew Charles. “Application of Organocatalysis to the Synthesis of Chiral Morpholines, Piperazines, Aziridines, Azetidines, beta-fluoroamines, and gamma-fluoroamines; Discovery of Selective Phospholipase D Inhibitors with Optimized in vivo Properties.” 2014. Web. 03 Dec 2020.

Vancouver:

O'Reilly MC. Application of Organocatalysis to the Synthesis of Chiral Morpholines, Piperazines, Aziridines, Azetidines, beta-fluoroamines, and gamma-fluoroamines; Discovery of Selective Phospholipase D Inhibitors with Optimized in vivo Properties. [Internet] [Doctoral dissertation]. Vanderbilt University; 2014. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/1803/12701.

Council of Science Editors:

O'Reilly MC. Application of Organocatalysis to the Synthesis of Chiral Morpholines, Piperazines, Aziridines, Azetidines, beta-fluoroamines, and gamma-fluoroamines; Discovery of Selective Phospholipase D Inhibitors with Optimized in vivo Properties. [Doctoral Dissertation]. Vanderbilt University; 2014. Available from: http://hdl.handle.net/1803/12701


University of Adelaide

3. Williams, Evan Hale. Some aspects of the conformation and stereochemistry of four-membered ring heterocycles / by Evan Hale Williams.

Degree: 1980, University of Adelaide

Subjects/Keywords: Heterocyclic compounds.; Azetidines.; Stereochemistry.; Conformational analysis.

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APA (6th Edition):

Williams, E. H. (1980). Some aspects of the conformation and stereochemistry of four-membered ring heterocycles / by Evan Hale Williams. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/21391

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):

Williams, Evan Hale. “Some aspects of the conformation and stereochemistry of four-membered ring heterocycles / by Evan Hale Williams.” 1980. Thesis, University of Adelaide. Accessed December 03, 2020. http://hdl.handle.net/2440/21391.

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

MLA Handbook (7th Edition):

Williams, Evan Hale. “Some aspects of the conformation and stereochemistry of four-membered ring heterocycles / by Evan Hale Williams.” 1980. Web. 03 Dec 2020.

Vancouver:

Williams EH. Some aspects of the conformation and stereochemistry of four-membered ring heterocycles / by Evan Hale Williams. [Internet] [Thesis]. University of Adelaide; 1980. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/2440/21391.

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

Council of Science Editors:

Williams EH. Some aspects of the conformation and stereochemistry of four-membered ring heterocycles / by Evan Hale Williams. [Thesis]. University of Adelaide; 1980. Available from: http://hdl.handle.net/2440/21391

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

4. Semina, Elena. Synthesis of new cyclic and acyclic biologically relevant amino acid derivatives.

Degree: 2016, Ghent University

 The discovery of non-proteinogenic amino acids among natural products has significantly increased interest in this class of compounds as they may possess interesting biological activity… (more)

Subjects/Keywords: Chemistry; Azetidines; Aziridines; Piperidines; Non-proteinogenic amino acids; Diversity oriented synthesis; Epoxides

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APA (6th Edition):

Semina, E. (2016). Synthesis of new cyclic and acyclic biologically relevant amino acid derivatives. (Thesis). Ghent University. Retrieved from http://hdl.handle.net/1854/LU-7041917

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):

Semina, Elena. “Synthesis of new cyclic and acyclic biologically relevant amino acid derivatives.” 2016. Thesis, Ghent University. Accessed December 03, 2020. http://hdl.handle.net/1854/LU-7041917.

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

MLA Handbook (7th Edition):

Semina, Elena. “Synthesis of new cyclic and acyclic biologically relevant amino acid derivatives.” 2016. Web. 03 Dec 2020.

Vancouver:

Semina E. Synthesis of new cyclic and acyclic biologically relevant amino acid derivatives. [Internet] [Thesis]. Ghent University; 2016. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/1854/LU-7041917.

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

Council of Science Editors:

Semina E. Synthesis of new cyclic and acyclic biologically relevant amino acid derivatives. [Thesis]. Ghent University; 2016. Available from: http://hdl.handle.net/1854/LU-7041917

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

5. Barré, Baptiste. Fonctionnalisation d'hétérocycles par des réactions métallo-catalysées : Heterocycles functionalization by metal-catalysed reactions.

Degree: Docteur es, Chimie Organique, 2016, Université Pierre et Marie Curie – Paris VI

Les réactions de couplage croisé ont révolutionné la chimie organique. Par exemple, dans le domaine de la chimie médicinale, les réactions de couplage sont de… (more)

Subjects/Keywords: Couplage croisé; Cobalt; Fer; Réactif de Grignard; Études mécanistiques; Voltampérométrie cyclique; Cobalt-Iron catalysed cross-coupling; Mechanistic study; Azetidines; 547

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APA (6th Edition):

Barré, B. (2016). Fonctionnalisation d'hétérocycles par des réactions métallo-catalysées : Heterocycles functionalization by metal-catalysed reactions. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2016PA066461

Chicago Manual of Style (16th Edition):

Barré, Baptiste. “Fonctionnalisation d'hétérocycles par des réactions métallo-catalysées : Heterocycles functionalization by metal-catalysed reactions.” 2016. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed December 03, 2020. http://www.theses.fr/2016PA066461.

MLA Handbook (7th Edition):

Barré, Baptiste. “Fonctionnalisation d'hétérocycles par des réactions métallo-catalysées : Heterocycles functionalization by metal-catalysed reactions.” 2016. Web. 03 Dec 2020.

Vancouver:

Barré B. Fonctionnalisation d'hétérocycles par des réactions métallo-catalysées : Heterocycles functionalization by metal-catalysed reactions. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2016. [cited 2020 Dec 03]. Available from: http://www.theses.fr/2016PA066461.

Council of Science Editors:

Barré B. Fonctionnalisation d'hétérocycles par des réactions métallo-catalysées : Heterocycles functionalization by metal-catalysed reactions. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2016. Available from: http://www.theses.fr/2016PA066461


University of New Orleans

6. Das, Madhurima. Synthesis and Evaluation of Novel Biologically Active Compounds.

Degree: PhD, Chemistry, 2020, University of New Orleans

  SCP-1, a potent derivative of acetaminophen, exhibits significantly diminished hepatotoxicity and nephrotoxicity relative to acetaminophen and nitrate ester derivatives of acetaminophen. It was therefore… (more)

Subjects/Keywords: NO donor; SCP-1; azetidines; Friedel-Crafts arylation; pyruvate esters; ozonolysis; Chemistry; Medicinal-Pharmaceutical Chemistry; Organic Chemistry

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APA (6th Edition):

Das, M. (2020). Synthesis and Evaluation of Novel Biologically Active Compounds. (Doctoral Dissertation). University of New Orleans. Retrieved from https://scholarworks.uno.edu/td/2736

Chicago Manual of Style (16th Edition):

Das, Madhurima. “Synthesis and Evaluation of Novel Biologically Active Compounds.” 2020. Doctoral Dissertation, University of New Orleans. Accessed December 03, 2020. https://scholarworks.uno.edu/td/2736.

MLA Handbook (7th Edition):

Das, Madhurima. “Synthesis and Evaluation of Novel Biologically Active Compounds.” 2020. Web. 03 Dec 2020.

Vancouver:

Das M. Synthesis and Evaluation of Novel Biologically Active Compounds. [Internet] [Doctoral dissertation]. University of New Orleans; 2020. [cited 2020 Dec 03]. Available from: https://scholarworks.uno.edu/td/2736.

Council of Science Editors:

Das M. Synthesis and Evaluation of Novel Biologically Active Compounds. [Doctoral Dissertation]. University of New Orleans; 2020. Available from: https://scholarworks.uno.edu/td/2736


University of New Orleans

7. Thaxton, Amber. Synthesis of Novel Azetidines.

Degree: PhD, Chemistry, 2013, University of New Orleans

  Azetidine is a four-membered nitrogen-containing heterocyclic ring that has recently received a great deal of attention as a molecular scaffold for the design and… (more)

Subjects/Keywords: Azetidines, Methamphetamine addiction, Monoamine re-uptake inhibitor, diarylheterocycles, Friedel-Crafts alkylation; Medicinal and Pharmaceutical Chemistry; Organic Chemistry

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APA (6th Edition):

Thaxton, A. (2013). Synthesis of Novel Azetidines. (Doctoral Dissertation). University of New Orleans. Retrieved from https://scholarworks.uno.edu/td/1764

Chicago Manual of Style (16th Edition):

Thaxton, Amber. “Synthesis of Novel Azetidines.” 2013. Doctoral Dissertation, University of New Orleans. Accessed December 03, 2020. https://scholarworks.uno.edu/td/1764.

MLA Handbook (7th Edition):

Thaxton, Amber. “Synthesis of Novel Azetidines.” 2013. Web. 03 Dec 2020.

Vancouver:

Thaxton A. Synthesis of Novel Azetidines. [Internet] [Doctoral dissertation]. University of New Orleans; 2013. [cited 2020 Dec 03]. Available from: https://scholarworks.uno.edu/td/1764.

Council of Science Editors:

Thaxton A. Synthesis of Novel Azetidines. [Doctoral Dissertation]. University of New Orleans; 2013. Available from: https://scholarworks.uno.edu/td/1764

8. Nocquet, Pierre-Antoine. Vers la synthèse d'une nouvelle classe d'iminosucres conformationnellement contraints : ouverture d'azétidines, cyclisation 4-exo-trig et C-H amination catalytique : Toward the synthesis of a new class of conformationally strained iminosugars : azetidine ring-opening, 4-exo-trig cyclization and catalytic C-H amination.

Degree: Docteur es, Chimie, 2013, Université de Strasbourg

De précédentes études dans notre groupe ont montré que l'α-1-C-nonyl-1,5-didésoxy-1,5-imino-D-xylitol était un inhibiteur puissant de la β-glucocérébrosidase, enzyme impliquée dans la maladie de Gaucher. Il… (more)

Subjects/Keywords: Iminosucres; Spirocycles; Azétidines; Réaction domino; Cyclisation radicalaire; 4-exo-trig; Carbasucres; C-H amination; Iminosugars; Spirocycles; Azetidines; Domino reaction; Radical cyclisation; 4-exo-trig; Carbasugars; C-H amination; 547.2

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APA (6th Edition):

Nocquet, P. (2013). Vers la synthèse d'une nouvelle classe d'iminosucres conformationnellement contraints : ouverture d'azétidines, cyclisation 4-exo-trig et C-H amination catalytique : Toward the synthesis of a new class of conformationally strained iminosugars : azetidine ring-opening, 4-exo-trig cyclization and catalytic C-H amination. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2013STRAF047

Chicago Manual of Style (16th Edition):

Nocquet, Pierre-Antoine. “Vers la synthèse d'une nouvelle classe d'iminosucres conformationnellement contraints : ouverture d'azétidines, cyclisation 4-exo-trig et C-H amination catalytique : Toward the synthesis of a new class of conformationally strained iminosugars : azetidine ring-opening, 4-exo-trig cyclization and catalytic C-H amination.” 2013. Doctoral Dissertation, Université de Strasbourg. Accessed December 03, 2020. http://www.theses.fr/2013STRAF047.

MLA Handbook (7th Edition):

Nocquet, Pierre-Antoine. “Vers la synthèse d'une nouvelle classe d'iminosucres conformationnellement contraints : ouverture d'azétidines, cyclisation 4-exo-trig et C-H amination catalytique : Toward the synthesis of a new class of conformationally strained iminosugars : azetidine ring-opening, 4-exo-trig cyclization and catalytic C-H amination.” 2013. Web. 03 Dec 2020.

Vancouver:

Nocquet P. Vers la synthèse d'une nouvelle classe d'iminosucres conformationnellement contraints : ouverture d'azétidines, cyclisation 4-exo-trig et C-H amination catalytique : Toward the synthesis of a new class of conformationally strained iminosugars : azetidine ring-opening, 4-exo-trig cyclization and catalytic C-H amination. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2013. [cited 2020 Dec 03]. Available from: http://www.theses.fr/2013STRAF047.

Council of Science Editors:

Nocquet P. Vers la synthèse d'une nouvelle classe d'iminosucres conformationnellement contraints : ouverture d'azétidines, cyclisation 4-exo-trig et C-H amination catalytique : Toward the synthesis of a new class of conformationally strained iminosugars : azetidine ring-opening, 4-exo-trig cyclization and catalytic C-H amination. [Doctoral Dissertation]. Université de Strasbourg; 2013. Available from: http://www.theses.fr/2013STRAF047

9. Kern, Nicolas. Réactivité d'azacycles en catalyse à l'or : Reactivities of N-heterocycles in gold catalysis.

Degree: Docteur es, Chimie organique, 2014, Université de Strasbourg

La catalyse organométallique est l'un des piliers de la synthèse chimique moderne. Elle permet notamment la formation rapide de liaisons carbone-carbone et carbone-hétéroatome, processus les… (more)

Subjects/Keywords: Catalyse homogène; Complexes d'or et d'argent; Hétérocycles acétyléniques; Aziridines; Azétidines; Spirocycles; Mitosènes; Groupements protecteurs; Homogenous catalysis; Gold complexes; Silver complexes; Aziridines; Azetidines; Spiro compounds; Mitosenes; Protectiong groups; 547.2

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APA (6th Edition):

Kern, N. (2014). Réactivité d'azacycles en catalyse à l'or : Reactivities of N-heterocycles in gold catalysis. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2014STRAF012

Chicago Manual of Style (16th Edition):

Kern, Nicolas. “Réactivité d'azacycles en catalyse à l'or : Reactivities of N-heterocycles in gold catalysis.” 2014. Doctoral Dissertation, Université de Strasbourg. Accessed December 03, 2020. http://www.theses.fr/2014STRAF012.

MLA Handbook (7th Edition):

Kern, Nicolas. “Réactivité d'azacycles en catalyse à l'or : Reactivities of N-heterocycles in gold catalysis.” 2014. Web. 03 Dec 2020.

Vancouver:

Kern N. Réactivité d'azacycles en catalyse à l'or : Reactivities of N-heterocycles in gold catalysis. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2014. [cited 2020 Dec 03]. Available from: http://www.theses.fr/2014STRAF012.

Council of Science Editors:

Kern N. Réactivité d'azacycles en catalyse à l'or : Reactivities of N-heterocycles in gold catalysis. [Doctoral Dissertation]. Université de Strasbourg; 2014. Available from: http://www.theses.fr/2014STRAF012

10. Slaughter, Kimari. Synthesis and Development of Potential CB1 Receptor Neutral Antagonists.

Degree: MS, Chemistry, 2012, University of New Orleans

  Cannabis and its derivatives have been used for both medicinal and recreational purposes. The study of this plant led to the discovery of over… (more)

Subjects/Keywords: Cannabinoids, Cannabinoid receptors, Dopamine, Benzhydryl Azetidines, Diols, Oximes, Amines; Medicinal-Pharmaceutical Chemistry; Organic Chemistry

…12 Table 2. N-Benzhydryl Azetidines… …Azetidines, Diols, Oximes, Amines viii receptors, Dopamine, Benzhydryl Introduction Cannabis… …Rationale The patent literature has reported that N-benzhydryl azetidines exhibit CB1 antagonist… …Benzhydrylazetidine 3 There is no reported structural-activity data for the series of azetidines represented… …patterns for the N-Ar region and S region of the azetidine targets. Synthesis of Azetidines… 

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

APA (6th Edition):

Slaughter, K. (2012). Synthesis and Development of Potential CB1 Receptor Neutral Antagonists. (Thesis). University of New Orleans. Retrieved from https://scholarworks.uno.edu/td/1483

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):

Slaughter, Kimari. “Synthesis and Development of Potential CB1 Receptor Neutral Antagonists.” 2012. Thesis, University of New Orleans. Accessed December 03, 2020. https://scholarworks.uno.edu/td/1483.

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

MLA Handbook (7th Edition):

Slaughter, Kimari. “Synthesis and Development of Potential CB1 Receptor Neutral Antagonists.” 2012. Web. 03 Dec 2020.

Vancouver:

Slaughter K. Synthesis and Development of Potential CB1 Receptor Neutral Antagonists. [Internet] [Thesis]. University of New Orleans; 2012. [cited 2020 Dec 03]. Available from: https://scholarworks.uno.edu/td/1483.

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

Council of Science Editors:

Slaughter K. Synthesis and Development of Potential CB1 Receptor Neutral Antagonists. [Thesis]. University of New Orleans; 2012. Available from: https://scholarworks.uno.edu/td/1483

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

.