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You searched for subject:(Aza peptide). Showing records 1 – 9 of 9 total matches.

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Vanderbilt University

1. Schwieter, Kenneth Edward. Toward On-Demand Peptide Synthesis: Development and Application of Enantioselective Syntheses of Unnatural α-Amino Amides.

Degree: PhD, Chemistry, 2016, Vanderbilt University

 Unnatural amino acid derived fragments are present in a multitude of pharmaceuticals and biologically relevant molecules including complex peptides. Current preparative methods focus almost entirely… (more)

Subjects/Keywords: peptide synthesis; umpolung; amide synthesis; amino acids; aza-Henry; organocatalysis

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

APA (6th Edition):

Schwieter, K. E. (2016). Toward On-Demand Peptide Synthesis: Development and Application of Enantioselective Syntheses of Unnatural α-Amino Amides. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14372

Chicago Manual of Style (16th Edition):

Schwieter, Kenneth Edward. “Toward On-Demand Peptide Synthesis: Development and Application of Enantioselective Syntheses of Unnatural α-Amino Amides.” 2016. Doctoral Dissertation, Vanderbilt University. Accessed January 26, 2021. http://hdl.handle.net/1803/14372.

MLA Handbook (7th Edition):

Schwieter, Kenneth Edward. “Toward On-Demand Peptide Synthesis: Development and Application of Enantioselective Syntheses of Unnatural α-Amino Amides.” 2016. Web. 26 Jan 2021.

Vancouver:

Schwieter KE. Toward On-Demand Peptide Synthesis: Development and Application of Enantioselective Syntheses of Unnatural α-Amino Amides. [Internet] [Doctoral dissertation]. Vanderbilt University; 2016. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/1803/14372.

Council of Science Editors:

Schwieter KE. Toward On-Demand Peptide Synthesis: Development and Application of Enantioselective Syntheses of Unnatural α-Amino Amides. [Doctoral Dissertation]. Vanderbilt University; 2016. Available from: http://hdl.handle.net/1803/14372


Georgia Tech

2. Campbell, Amy. Design, Synthesis, and Evaluation of Cysteine Protease Inhibitors.

Degree: PhD, Chemistry and Biochemistry, 2005, Georgia Tech

 Both clan CA and clan CD proteases have a variety of physiological and pathological roles. In particular, both clans have members who have been implicated… (more)

Subjects/Keywords: Epoxysuccinyl aza-peptides; Molecular modeling; Caspases; Irreversible kinetics; Aza-peptide epoxides

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APA (6th Edition):

Campbell, A. (2005). Design, Synthesis, and Evaluation of Cysteine Protease Inhibitors. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/14046

Chicago Manual of Style (16th Edition):

Campbell, Amy. “Design, Synthesis, and Evaluation of Cysteine Protease Inhibitors.” 2005. Doctoral Dissertation, Georgia Tech. Accessed January 26, 2021. http://hdl.handle.net/1853/14046.

MLA Handbook (7th Edition):

Campbell, Amy. “Design, Synthesis, and Evaluation of Cysteine Protease Inhibitors.” 2005. Web. 26 Jan 2021.

Vancouver:

Campbell A. Design, Synthesis, and Evaluation of Cysteine Protease Inhibitors. [Internet] [Doctoral dissertation]. Georgia Tech; 2005. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/1853/14046.

Council of Science Editors:

Campbell A. Design, Synthesis, and Evaluation of Cysteine Protease Inhibitors. [Doctoral Dissertation]. Georgia Tech; 2005. Available from: http://hdl.handle.net/1853/14046

3. Besret, Soizic. Ligations chimiques : synthèse d'inhibiteurs extracellulaires de la signalisation HGF/SF-MET : Chemical Ligation Synthesis of extracellular inhibitors of HGF/SF-MET signalling pathway.

Degree: Docteur es, Sciences du médicament, 2011, Université Lille II – Droit et Santé

Les peptides constituent une famille de biomolécules dont l’utilisation dans différents domaines thérapeutiques (cancer, diabète, sida) s’est fortement développée ces dernières années. Le défi pour… (more)

Subjects/Keywords: Ligations chimiques; Ligations peptidiques; Aza Glypeptide; Inhibiteurs de MET; Proto Oncogene Proteins c met; Peptide Library

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APA (6th Edition):

Besret, S. (2011). Ligations chimiques : synthèse d'inhibiteurs extracellulaires de la signalisation HGF/SF-MET : Chemical Ligation Synthesis of extracellular inhibitors of HGF/SF-MET signalling pathway. (Doctoral Dissertation). Université Lille II – Droit et Santé. Retrieved from http://www.theses.fr/2011LIL2S003

Chicago Manual of Style (16th Edition):

Besret, Soizic. “Ligations chimiques : synthèse d'inhibiteurs extracellulaires de la signalisation HGF/SF-MET : Chemical Ligation Synthesis of extracellular inhibitors of HGF/SF-MET signalling pathway.” 2011. Doctoral Dissertation, Université Lille II – Droit et Santé. Accessed January 26, 2021. http://www.theses.fr/2011LIL2S003.

MLA Handbook (7th Edition):

Besret, Soizic. “Ligations chimiques : synthèse d'inhibiteurs extracellulaires de la signalisation HGF/SF-MET : Chemical Ligation Synthesis of extracellular inhibitors of HGF/SF-MET signalling pathway.” 2011. Web. 26 Jan 2021.

Vancouver:

Besret S. Ligations chimiques : synthèse d'inhibiteurs extracellulaires de la signalisation HGF/SF-MET : Chemical Ligation Synthesis of extracellular inhibitors of HGF/SF-MET signalling pathway. [Internet] [Doctoral dissertation]. Université Lille II – Droit et Santé 2011. [cited 2021 Jan 26]. Available from: http://www.theses.fr/2011LIL2S003.

Council of Science Editors:

Besret S. Ligations chimiques : synthèse d'inhibiteurs extracellulaires de la signalisation HGF/SF-MET : Chemical Ligation Synthesis of extracellular inhibitors of HGF/SF-MET signalling pathway. [Doctoral Dissertation]. Université Lille II – Droit et Santé 2011. Available from: http://www.theses.fr/2011LIL2S003


Vanderbilt University

4. Makley, Dawn Marie. Umpolung amide synthesis: applications in enantioselective peptide synthesis.

Degree: PhD, Chemistry, 2012, Vanderbilt University

 UMPOLUNG AMIDE SYNTHESIS: APPLICATIONS IN ENANTIOSELECTIVE PEPTIDE SYNTHESISDAWN M. MAKLEYDissertation under the direction of Professor Jeffrey N. JohnstonThe development and application of the novel Umpolung… (more)

Subjects/Keywords: silyl imines; n-halo amines; natural product synthesis; peptide synthesis; amide synthesis; umpolung; methodology development; chemistry; aza-Henry; umpolung amide synthesis; UmAS

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

APA (6th Edition):

Makley, D. M. (2012). Umpolung amide synthesis: applications in enantioselective peptide synthesis. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14598

Chicago Manual of Style (16th Edition):

Makley, Dawn Marie. “Umpolung amide synthesis: applications in enantioselective peptide synthesis.” 2012. Doctoral Dissertation, Vanderbilt University. Accessed January 26, 2021. http://hdl.handle.net/1803/14598.

MLA Handbook (7th Edition):

Makley, Dawn Marie. “Umpolung amide synthesis: applications in enantioselective peptide synthesis.” 2012. Web. 26 Jan 2021.

Vancouver:

Makley DM. Umpolung amide synthesis: applications in enantioselective peptide synthesis. [Internet] [Doctoral dissertation]. Vanderbilt University; 2012. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/1803/14598.

Council of Science Editors:

Makley DM. Umpolung amide synthesis: applications in enantioselective peptide synthesis. [Doctoral Dissertation]. Vanderbilt University; 2012. Available from: http://hdl.handle.net/1803/14598


Vanderbilt University

5. Shen, Bo. New Enantioselective Approaches to the Synthesis of Amino Acid Derivatives and Peptides Using Chiral Proton Catalysis.

Degree: PhD, Chemistry, 2010, Vanderbilt University

 α,β-Diamino acids and β-amino acids are important constituents in countless natural products. These atypical amino acids often display interesting and useful biological properties and have… (more)

Subjects/Keywords: Chiral Proton Catalysis; Enantioselective; Amino Acid; Peptide synthesis; aza-Henry reaction

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APA (6th Edition):

Shen, B. (2010). New Enantioselective Approaches to the Synthesis of Amino Acid Derivatives and Peptides Using Chiral Proton Catalysis. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/11772

Chicago Manual of Style (16th Edition):

Shen, Bo. “New Enantioselective Approaches to the Synthesis of Amino Acid Derivatives and Peptides Using Chiral Proton Catalysis.” 2010. Doctoral Dissertation, Vanderbilt University. Accessed January 26, 2021. http://hdl.handle.net/1803/11772.

MLA Handbook (7th Edition):

Shen, Bo. “New Enantioselective Approaches to the Synthesis of Amino Acid Derivatives and Peptides Using Chiral Proton Catalysis.” 2010. Web. 26 Jan 2021.

Vancouver:

Shen B. New Enantioselective Approaches to the Synthesis of Amino Acid Derivatives and Peptides Using Chiral Proton Catalysis. [Internet] [Doctoral dissertation]. Vanderbilt University; 2010. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/1803/11772.

Council of Science Editors:

Shen B. New Enantioselective Approaches to the Synthesis of Amino Acid Derivatives and Peptides Using Chiral Proton Catalysis. [Doctoral Dissertation]. Vanderbilt University; 2010. Available from: http://hdl.handle.net/1803/11772


Georgia Tech

6. Gotz, Marion Gabriele. Design, synthesis, and evaluation of irreversible peptidyl inhibitors for clan CA and clan CD cysteine proteases.

Degree: PhD, Chemistry and Biochemistry, 2004, Georgia Tech

 Cysteine proteases are a class of proteolytic enzymes, which are involved in a series of metabolic and catabolic processes, such as protein turnover, digestion, blood… (more)

Subjects/Keywords: Allyl sulfone; Aza-peptide; Biosynthesis; Cysteine protease; Cysteine proteinases; Irreversible inhibitors; Protease inhibitors; Sulphones; Vinyl sulfone

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

APA (6th Edition):

Gotz, M. G. (2004). Design, synthesis, and evaluation of irreversible peptidyl inhibitors for clan CA and clan CD cysteine proteases. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/8072

Chicago Manual of Style (16th Edition):

Gotz, Marion Gabriele. “Design, synthesis, and evaluation of irreversible peptidyl inhibitors for clan CA and clan CD cysteine proteases.” 2004. Doctoral Dissertation, Georgia Tech. Accessed January 26, 2021. http://hdl.handle.net/1853/8072.

MLA Handbook (7th Edition):

Gotz, Marion Gabriele. “Design, synthesis, and evaluation of irreversible peptidyl inhibitors for clan CA and clan CD cysteine proteases.” 2004. Web. 26 Jan 2021.

Vancouver:

Gotz MG. Design, synthesis, and evaluation of irreversible peptidyl inhibitors for clan CA and clan CD cysteine proteases. [Internet] [Doctoral dissertation]. Georgia Tech; 2004. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/1853/8072.

Council of Science Editors:

Gotz MG. Design, synthesis, and evaluation of irreversible peptidyl inhibitors for clan CA and clan CD cysteine proteases. [Doctoral Dissertation]. Georgia Tech; 2004. Available from: http://hdl.handle.net/1853/8072

7. Chingle, Ramesh. Design, synthesis, pericyclic chemistry and biomedical applications of azopeptides.

Degree: 2018, Université de Montréal

Subjects/Keywords: Azapeptides; Peptidomimétique; Tour β; Semicarbazone; Aza-valine; Semicarbazide; Azopeptide; Aza-Diels Alder; Alder-ene; Péricyclique; GHRP-6; Récepteur GHS-R1a; Récepteur CD36; Peptide mimicry; β-turn; Pericyclic; Chemistry - Organic / Chimie organique (UMI : 0490)

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APA (6th Edition):

Chingle, R. (2018). Design, synthesis, pericyclic chemistry and biomedical applications of azopeptides. (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/20753

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):

Chingle, Ramesh. “Design, synthesis, pericyclic chemistry and biomedical applications of azopeptides.” 2018. Thesis, Université de Montréal. Accessed January 26, 2021. http://hdl.handle.net/1866/20753.

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

MLA Handbook (7th Edition):

Chingle, Ramesh. “Design, synthesis, pericyclic chemistry and biomedical applications of azopeptides.” 2018. Web. 26 Jan 2021.

Vancouver:

Chingle R. Design, synthesis, pericyclic chemistry and biomedical applications of azopeptides. [Internet] [Thesis]. Université de Montréal; 2018. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/1866/20753.

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

Council of Science Editors:

Chingle R. Design, synthesis, pericyclic chemistry and biomedical applications of azopeptides. [Thesis]. Université de Montréal; 2018. Available from: http://hdl.handle.net/1866/20753

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


Université de Montréal

8. Mohammadpourmir, Fatemeh. Synthesis of Aza- and α,α-disubstituted Glycinyl peptides and application of their electronic and steric interactions for controlling peptide folding, and for biomedical applications.

Degree: 2019, Université de Montréal

Subjects/Keywords: Peptidomimetic; Azapeptide; Prostaglandin F2alpha; Aza-propargylglycine; alpha-turn; gamma-turn; Cα-disubstituted glycine; peptide folding; 2-amino adamantane-2-carboxylic acid; torsion angle; Peptidomimétique; Prostaglandine F2alpha; Tour-alpha; Tour-beta; Tour-gamma; Acides aminés Calpha-di-substitués; Repliement peptidique; Acide-2-amino-2-adamantane; Angle de torsion; Chemistry - Organic / Chimie organique (UMI : 0490)

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APA (6th Edition):

Mohammadpourmir, F. (2019). Synthesis of Aza- and α,α-disubstituted Glycinyl peptides and application of their electronic and steric interactions for controlling peptide folding, and for biomedical applications. (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/21698

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):

Mohammadpourmir, Fatemeh. “Synthesis of Aza- and α,α-disubstituted Glycinyl peptides and application of their electronic and steric interactions for controlling peptide folding, and for biomedical applications.” 2019. Thesis, Université de Montréal. Accessed January 26, 2021. http://hdl.handle.net/1866/21698.

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

MLA Handbook (7th Edition):

Mohammadpourmir, Fatemeh. “Synthesis of Aza- and α,α-disubstituted Glycinyl peptides and application of their electronic and steric interactions for controlling peptide folding, and for biomedical applications.” 2019. Web. 26 Jan 2021.

Vancouver:

Mohammadpourmir F. Synthesis of Aza- and α,α-disubstituted Glycinyl peptides and application of their electronic and steric interactions for controlling peptide folding, and for biomedical applications. [Internet] [Thesis]. Université de Montréal; 2019. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/1866/21698.

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

Council of Science Editors:

Mohammadpourmir F. Synthesis of Aza- and α,α-disubstituted Glycinyl peptides and application of their electronic and steric interactions for controlling peptide folding, and for biomedical applications. [Thesis]. Université de Montréal; 2019. Available from: http://hdl.handle.net/1866/21698

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


Université de Montréal

9. Proulx, Caroline. Méthodologie pour la synthèse combinatoire d’azapeptides: application à la synthèse d’analogues aza-GHRP-6 en tant que ligands du récepteur CD36.

Degree: 2012, Université de Montréal

Subjects/Keywords: Azapeptides; Repliement beta; Mimes peptidiques; GHRP-6; Récepteur GHS-R1a; Récepteur CD36; Angiogénèse; Semicarbazone; N-Alkylation; N-Arylation; Aza-propargylglycine; Cycloaddition 1,3-dipolaire; Couplage A3; N-amino-imidazolin-2-ones; Beta turn; Peptide mimicry; GHS-R1a receptor; CD36 receptor; Angiogenesis; 1,3-Dipolar cycloaddition; A3 coupling; Chemistry - Organic / Chimie organique (UMI : 0490)

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APA (6th Edition):

Proulx, C. (2012). Méthodologie pour la synthèse combinatoire d’azapeptides: application à la synthèse d’analogues aza-GHRP-6 en tant que ligands du récepteur CD36. (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/8887

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):

Proulx, Caroline. “Méthodologie pour la synthèse combinatoire d’azapeptides: application à la synthèse d’analogues aza-GHRP-6 en tant que ligands du récepteur CD36.” 2012. Thesis, Université de Montréal. Accessed January 26, 2021. http://hdl.handle.net/1866/8887.

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

MLA Handbook (7th Edition):

Proulx, Caroline. “Méthodologie pour la synthèse combinatoire d’azapeptides: application à la synthèse d’analogues aza-GHRP-6 en tant que ligands du récepteur CD36.” 2012. Web. 26 Jan 2021.

Vancouver:

Proulx C. Méthodologie pour la synthèse combinatoire d’azapeptides: application à la synthèse d’analogues aza-GHRP-6 en tant que ligands du récepteur CD36. [Internet] [Thesis]. Université de Montréal; 2012. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/1866/8887.

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

Council of Science Editors:

Proulx C. Méthodologie pour la synthèse combinatoire d’azapeptides: application à la synthèse d’analogues aza-GHRP-6 en tant que ligands du récepteur CD36. [Thesis]. Université de Montréal; 2012. Available from: http://hdl.handle.net/1866/8887

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

.