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You searched for subject:(Aziridines). Showing records 1 – 30 of 40 total matches.

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Texas Tech University

1. Xue, Zheng. Catalytic aziridinations and daisy chain polymer syntheses.

Degree: Chemistry, 2009, Texas Tech University

 Methodological development toward the synthesis of useful molecular building blocks serves as a powerful toolbox for complex molecule syntheses and is essential in scientific fields… (more)

Subjects/Keywords: Aziridines

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APA (6th Edition):

Xue, Z. (2009). Catalytic aziridinations and daisy chain polymer syntheses. (Thesis). Texas Tech University. Retrieved from http://hdl.handle.net/2346/22097

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):

Xue, Zheng. “Catalytic aziridinations and daisy chain polymer syntheses.” 2009. Thesis, Texas Tech University. Accessed December 04, 2020. http://hdl.handle.net/2346/22097.

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

MLA Handbook (7th Edition):

Xue, Zheng. “Catalytic aziridinations and daisy chain polymer syntheses.” 2009. Web. 04 Dec 2020.

Vancouver:

Xue Z. Catalytic aziridinations and daisy chain polymer syntheses. [Internet] [Thesis]. Texas Tech University; 2009. [cited 2020 Dec 04]. Available from: http://hdl.handle.net/2346/22097.

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

Council of Science Editors:

Xue Z. Catalytic aziridinations and daisy chain polymer syntheses. [Thesis]. Texas Tech University; 2009. Available from: http://hdl.handle.net/2346/22097

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


Michigan State University

2. Lu, Zhenjie. Studies on the optimization of catalytic asymmetric aziridination reaction : tactics and mechanism.

Degree: PhD, Department of Chemistry, 2008, Michigan State University

Subjects/Keywords: Aziridines; Asymmetric synthesis

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APA (6th Edition):

Lu, Z. (2008). Studies on the optimization of catalytic asymmetric aziridination reaction : tactics and mechanism. (Doctoral Dissertation). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:47475

Chicago Manual of Style (16th Edition):

Lu, Zhenjie. “Studies on the optimization of catalytic asymmetric aziridination reaction : tactics and mechanism.” 2008. Doctoral Dissertation, Michigan State University. Accessed December 04, 2020. http://etd.lib.msu.edu/islandora/object/etd:47475.

MLA Handbook (7th Edition):

Lu, Zhenjie. “Studies on the optimization of catalytic asymmetric aziridination reaction : tactics and mechanism.” 2008. Web. 04 Dec 2020.

Vancouver:

Lu Z. Studies on the optimization of catalytic asymmetric aziridination reaction : tactics and mechanism. [Internet] [Doctoral dissertation]. Michigan State University; 2008. [cited 2020 Dec 04]. Available from: http://etd.lib.msu.edu/islandora/object/etd:47475.

Council of Science Editors:

Lu Z. Studies on the optimization of catalytic asymmetric aziridination reaction : tactics and mechanism. [Doctoral Dissertation]. Michigan State University; 2008. Available from: http://etd.lib.msu.edu/islandora/object/etd:47475

3. Gayon, Eric. Stratégies pour l'accès rapide à des hétérocycles azotés à partir d'alcools propargyliques : Rapid strategies to nitrogen heterocycles from propargylic alcohols.

Degree: Docteur es, Chimie organique, 2012, Montpellier, Ecole nationale supérieure de chimie; Ecole nationale supérieure de chimie (Montpellier)

La partie principale de ce manuscrit traite du développement de nouvelles méthodologies utilisant la substitution propargylique catalysée par des sels de fer(III), pour la formation… (more)

Subjects/Keywords: Substitutions propargyliques; Cyclisation; Catalyse; Isoxazoles; Aziridines; Pyrimidines; Propargylic substitution; Cyclization; Catalysis; Isoxazoles; Aziridines; Pyrimidines

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APA (6th Edition):

Gayon, E. (2012). Stratégies pour l'accès rapide à des hétérocycles azotés à partir d'alcools propargyliques : Rapid strategies to nitrogen heterocycles from propargylic alcohols. (Doctoral Dissertation). Montpellier, Ecole nationale supérieure de chimie; Ecole nationale supérieure de chimie (Montpellier). Retrieved from http://www.theses.fr/2012ENCM0017

Chicago Manual of Style (16th Edition):

Gayon, Eric. “Stratégies pour l'accès rapide à des hétérocycles azotés à partir d'alcools propargyliques : Rapid strategies to nitrogen heterocycles from propargylic alcohols.” 2012. Doctoral Dissertation, Montpellier, Ecole nationale supérieure de chimie; Ecole nationale supérieure de chimie (Montpellier). Accessed December 04, 2020. http://www.theses.fr/2012ENCM0017.

MLA Handbook (7th Edition):

Gayon, Eric. “Stratégies pour l'accès rapide à des hétérocycles azotés à partir d'alcools propargyliques : Rapid strategies to nitrogen heterocycles from propargylic alcohols.” 2012. Web. 04 Dec 2020.

Vancouver:

Gayon E. Stratégies pour l'accès rapide à des hétérocycles azotés à partir d'alcools propargyliques : Rapid strategies to nitrogen heterocycles from propargylic alcohols. [Internet] [Doctoral dissertation]. Montpellier, Ecole nationale supérieure de chimie; Ecole nationale supérieure de chimie (Montpellier); 2012. [cited 2020 Dec 04]. Available from: http://www.theses.fr/2012ENCM0017.

Council of Science Editors:

Gayon E. Stratégies pour l'accès rapide à des hétérocycles azotés à partir d'alcools propargyliques : Rapid strategies to nitrogen heterocycles from propargylic alcohols. [Doctoral Dissertation]. Montpellier, Ecole nationale supérieure de chimie; Ecole nationale supérieure de chimie (Montpellier); 2012. Available from: http://www.theses.fr/2012ENCM0017

4. Ouerfelli, Oussema. Aziridine-2-carboxylates et leurs dérivées : Nouvelles perspectives en synthèse hétérocycliques et chimie des peptides. : Aziridine-2-carboxylate and their derivatives : New perspectives heterocyclic synthesis.

Degree: Docteur es, Chimie - Cergy, 2018, Cergy-Pontoise; Université de Tunis El Manar

L’objectif de cette thèse est d’élargir la gamme des composés issus des aziridine-2-carboxylates, obtenues par leur utilisation comme matière première pour la synthèse d’azahétérocycles ciblés… (more)

Subjects/Keywords: Chimie de fluor; Chimie hétérocyclique; Aziridines; Chimie de fluor; Chimie de fluor; Ring expansion; Aziridines; Ring expansion; Ring expansion; Aminoacids

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APA (6th Edition):

Ouerfelli, O. (2018). Aziridine-2-carboxylates et leurs dérivées : Nouvelles perspectives en synthèse hétérocycliques et chimie des peptides. : Aziridine-2-carboxylate and their derivatives : New perspectives heterocyclic synthesis. (Doctoral Dissertation). Cergy-Pontoise; Université de Tunis El Manar. Retrieved from http://www.theses.fr/2018CERG0973

Chicago Manual of Style (16th Edition):

Ouerfelli, Oussema. “Aziridine-2-carboxylates et leurs dérivées : Nouvelles perspectives en synthèse hétérocycliques et chimie des peptides. : Aziridine-2-carboxylate and their derivatives : New perspectives heterocyclic synthesis.” 2018. Doctoral Dissertation, Cergy-Pontoise; Université de Tunis El Manar. Accessed December 04, 2020. http://www.theses.fr/2018CERG0973.

MLA Handbook (7th Edition):

Ouerfelli, Oussema. “Aziridine-2-carboxylates et leurs dérivées : Nouvelles perspectives en synthèse hétérocycliques et chimie des peptides. : Aziridine-2-carboxylate and their derivatives : New perspectives heterocyclic synthesis.” 2018. Web. 04 Dec 2020.

Vancouver:

Ouerfelli O. Aziridine-2-carboxylates et leurs dérivées : Nouvelles perspectives en synthèse hétérocycliques et chimie des peptides. : Aziridine-2-carboxylate and their derivatives : New perspectives heterocyclic synthesis. [Internet] [Doctoral dissertation]. Cergy-Pontoise; Université de Tunis El Manar; 2018. [cited 2020 Dec 04]. Available from: http://www.theses.fr/2018CERG0973.

Council of Science Editors:

Ouerfelli O. Aziridine-2-carboxylates et leurs dérivées : Nouvelles perspectives en synthèse hétérocycliques et chimie des peptides. : Aziridine-2-carboxylate and their derivatives : New perspectives heterocyclic synthesis. [Doctoral Dissertation]. Cergy-Pontoise; Université de Tunis El Manar; 2018. Available from: http://www.theses.fr/2018CERG0973


Vanderbilt University

5. 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 04, 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. 04 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 04]. 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


Vanderbilt University

6. Schulte, Michael Lawrence. Application of Organocatalysis to the Synthesis of Pharmaceutically Relevant Scaffolds: Chiral Aziridines and β-Fluoroamines; Total Synthesis of Stemaphylline; and Discovery of Selective PAR4 Antagonists.

Degree: PhD, Chemistry, 2013, Vanderbilt University

Aziridines represent an important class of nitrogen-containing heterocycles with a wide range of synthetic utility. Despite their value, synthetic approaches are limited in terms of… (more)

Subjects/Keywords: organocatalysis; aziridines; fluoroamines; stemaphylline; stemaphylline N-oxide; protease activated receptor

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APA (6th Edition):

Schulte, M. L. (2013). Application of Organocatalysis to the Synthesis of Pharmaceutically Relevant Scaffolds: Chiral Aziridines and β-Fluoroamines; Total Synthesis of Stemaphylline; and Discovery of Selective PAR4 Antagonists. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/13263

Chicago Manual of Style (16th Edition):

Schulte, Michael Lawrence. “Application of Organocatalysis to the Synthesis of Pharmaceutically Relevant Scaffolds: Chiral Aziridines and β-Fluoroamines; Total Synthesis of Stemaphylline; and Discovery of Selective PAR4 Antagonists.” 2013. Doctoral Dissertation, Vanderbilt University. Accessed December 04, 2020. http://hdl.handle.net/1803/13263.

MLA Handbook (7th Edition):

Schulte, Michael Lawrence. “Application of Organocatalysis to the Synthesis of Pharmaceutically Relevant Scaffolds: Chiral Aziridines and β-Fluoroamines; Total Synthesis of Stemaphylline; and Discovery of Selective PAR4 Antagonists.” 2013. Web. 04 Dec 2020.

Vancouver:

Schulte ML. Application of Organocatalysis to the Synthesis of Pharmaceutically Relevant Scaffolds: Chiral Aziridines and β-Fluoroamines; Total Synthesis of Stemaphylline; and Discovery of Selective PAR4 Antagonists. [Internet] [Doctoral dissertation]. Vanderbilt University; 2013. [cited 2020 Dec 04]. Available from: http://hdl.handle.net/1803/13263.

Council of Science Editors:

Schulte ML. Application of Organocatalysis to the Synthesis of Pharmaceutically Relevant Scaffolds: Chiral Aziridines and β-Fluoroamines; Total Synthesis of Stemaphylline; and Discovery of Selective PAR4 Antagonists. [Doctoral Dissertation]. Vanderbilt University; 2013. Available from: http://hdl.handle.net/1803/13263


University of Oxford

7. Frost, Aileen Bernadette. Aziridines and aziridinium intermediates in the asymmetric synthesis of beta-substituted-alpha-amino acids and 1,2,3,4-tetrahydroisoquinolines.

Degree: PhD, 2015, University of Oxford

 This thesis is concerned with the development of methodology for the regioselective ring-opening of aziridines and aziridinium intermediates and its subsequent application to the asymmetric… (more)

Subjects/Keywords: 547; Organic chemistry; Aziridines; Aziridiniums; Amino Acids; Tetrahydroisoquinolines; Lithium Amide

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APA (6th Edition):

Frost, A. B. (2015). Aziridines and aziridinium intermediates in the asymmetric synthesis of beta-substituted-alpha-amino acids and 1,2,3,4-tetrahydroisoquinolines. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:ab3aa702-caab-4d20-9057-028258be5fdb ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.658517

Chicago Manual of Style (16th Edition):

Frost, Aileen Bernadette. “Aziridines and aziridinium intermediates in the asymmetric synthesis of beta-substituted-alpha-amino acids and 1,2,3,4-tetrahydroisoquinolines.” 2015. Doctoral Dissertation, University of Oxford. Accessed December 04, 2020. http://ora.ox.ac.uk/objects/uuid:ab3aa702-caab-4d20-9057-028258be5fdb ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.658517.

MLA Handbook (7th Edition):

Frost, Aileen Bernadette. “Aziridines and aziridinium intermediates in the asymmetric synthesis of beta-substituted-alpha-amino acids and 1,2,3,4-tetrahydroisoquinolines.” 2015. Web. 04 Dec 2020.

Vancouver:

Frost AB. Aziridines and aziridinium intermediates in the asymmetric synthesis of beta-substituted-alpha-amino acids and 1,2,3,4-tetrahydroisoquinolines. [Internet] [Doctoral dissertation]. University of Oxford; 2015. [cited 2020 Dec 04]. Available from: http://ora.ox.ac.uk/objects/uuid:ab3aa702-caab-4d20-9057-028258be5fdb ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.658517.

Council of Science Editors:

Frost AB. Aziridines and aziridinium intermediates in the asymmetric synthesis of beta-substituted-alpha-amino acids and 1,2,3,4-tetrahydroisoquinolines. [Doctoral Dissertation]. University of Oxford; 2015. Available from: http://ora.ox.ac.uk/objects/uuid:ab3aa702-caab-4d20-9057-028258be5fdb ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.658517


University of Edinburgh

8. Thomson, Dian Elizabeth. Approaches to chiral aziridination : formation and thermal rearrangements of N-ethoxycarbonylaziridines.

Degree: PhD, 1988, University of Edinburgh

Subjects/Keywords: 547; Synthesis of aziridines

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APA (6th Edition):

Thomson, D. E. (1988). Approaches to chiral aziridination : formation and thermal rearrangements of N-ethoxycarbonylaziridines. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/13121

Chicago Manual of Style (16th Edition):

Thomson, Dian Elizabeth. “Approaches to chiral aziridination : formation and thermal rearrangements of N-ethoxycarbonylaziridines.” 1988. Doctoral Dissertation, University of Edinburgh. Accessed December 04, 2020. http://hdl.handle.net/1842/13121.

MLA Handbook (7th Edition):

Thomson, Dian Elizabeth. “Approaches to chiral aziridination : formation and thermal rearrangements of N-ethoxycarbonylaziridines.” 1988. Web. 04 Dec 2020.

Vancouver:

Thomson DE. Approaches to chiral aziridination : formation and thermal rearrangements of N-ethoxycarbonylaziridines. [Internet] [Doctoral dissertation]. University of Edinburgh; 1988. [cited 2020 Dec 04]. Available from: http://hdl.handle.net/1842/13121.

Council of Science Editors:

Thomson DE. Approaches to chiral aziridination : formation and thermal rearrangements of N-ethoxycarbonylaziridines. [Doctoral Dissertation]. University of Edinburgh; 1988. Available from: http://hdl.handle.net/1842/13121


Loughborough University

9. Toon, Richard Clive. A study of directed cleavage of aziridinylcarbinyl radicals.

Degree: PhD, 1998, Loughborough University

 The work described in this thesis is an investigation into the reactivity and possible synthetic applications of aziridinylcarbinyl radicals. These radicals rapidly rearrange via β… (more)

Subjects/Keywords: 547; Free radicals; Aziridines; Aminyl

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APA (6th Edition):

Toon, R. C. (1998). A study of directed cleavage of aziridinylcarbinyl radicals. (Doctoral Dissertation). Loughborough University. Retrieved from http://hdl.handle.net/2134/13710

Chicago Manual of Style (16th Edition):

Toon, Richard Clive. “A study of directed cleavage of aziridinylcarbinyl radicals.” 1998. Doctoral Dissertation, Loughborough University. Accessed December 04, 2020. http://hdl.handle.net/2134/13710.

MLA Handbook (7th Edition):

Toon, Richard Clive. “A study of directed cleavage of aziridinylcarbinyl radicals.” 1998. Web. 04 Dec 2020.

Vancouver:

Toon RC. A study of directed cleavage of aziridinylcarbinyl radicals. [Internet] [Doctoral dissertation]. Loughborough University; 1998. [cited 2020 Dec 04]. Available from: http://hdl.handle.net/2134/13710.

Council of Science Editors:

Toon RC. A study of directed cleavage of aziridinylcarbinyl radicals. [Doctoral Dissertation]. Loughborough University; 1998. Available from: http://hdl.handle.net/2134/13710

10. Katampe, Ibrahim. The synthesis and reactions of silylaziridines.

Degree: PhD, 2000, Open University

 The reaction of an α-trialkylsilylvinyl carbanion and carboxylic acid derivatives gives α,β-unsaturated carbonyl compounds which, under the conditions of the reaction undergo further conjugate additiorn.… (more)

Subjects/Keywords: 547; Silicon-containing aziridines

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APA (6th Edition):

Katampe, I. (2000). The synthesis and reactions of silylaziridines. (Doctoral Dissertation). Open University. Retrieved from http://oro.open.ac.uk/63836/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.323273

Chicago Manual of Style (16th Edition):

Katampe, Ibrahim. “The synthesis and reactions of silylaziridines.” 2000. Doctoral Dissertation, Open University. Accessed December 04, 2020. http://oro.open.ac.uk/63836/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.323273.

MLA Handbook (7th Edition):

Katampe, Ibrahim. “The synthesis and reactions of silylaziridines.” 2000. Web. 04 Dec 2020.

Vancouver:

Katampe I. The synthesis and reactions of silylaziridines. [Internet] [Doctoral dissertation]. Open University; 2000. [cited 2020 Dec 04]. Available from: http://oro.open.ac.uk/63836/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.323273.

Council of Science Editors:

Katampe I. The synthesis and reactions of silylaziridines. [Doctoral Dissertation]. Open University; 2000. Available from: http://oro.open.ac.uk/63836/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.323273

11. 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 04, 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. 04 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 04]. 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


Université Paris-Sud – Paris XI

12. Malik, Guillaume. Développements méthodologiques pour la préparation de composés à visée anticancéreuse. : accès à des analogues du TMC-95A et synthèse totale de la Spisulosine et de son analogue fluoré : Synthetic methods for the preparation of new anti-cancer compounds : acces to new TMC-95A analogs and total synthesis of Spisulosine and its fluoro analog.

Degree: Docteur es, Chimie organique, 2011, Université Paris-Sud – Paris XI

Ce manuscrit expose différents développements méthodolgiques et leurs applications pour la synthèse de composés à visée anticancéreuse.Le premier chapitre décrit les travaux ciblant l’obtention d’analogues… (more)

Subjects/Keywords: TMC-95A; Fluoration; Insertion C-H; Aziridines; Sulfamates; Asymétrique; Spisulosine; Monanchorine; TMC-95A; Fluoration; C-H insertion; Aziridines; Sulfamates; Asymetrique; Spisulosine; Monanchorine

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APA (6th Edition):

Malik, G. (2011). Développements méthodologiques pour la préparation de composés à visée anticancéreuse. : accès à des analogues du TMC-95A et synthèse totale de la Spisulosine et de son analogue fluoré : Synthetic methods for the preparation of new anti-cancer compounds : acces to new TMC-95A analogs and total synthesis of Spisulosine and its fluoro analog. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2011PA112250

Chicago Manual of Style (16th Edition):

Malik, Guillaume. “Développements méthodologiques pour la préparation de composés à visée anticancéreuse. : accès à des analogues du TMC-95A et synthèse totale de la Spisulosine et de son analogue fluoré : Synthetic methods for the preparation of new anti-cancer compounds : acces to new TMC-95A analogs and total synthesis of Spisulosine and its fluoro analog.” 2011. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed December 04, 2020. http://www.theses.fr/2011PA112250.

MLA Handbook (7th Edition):

Malik, Guillaume. “Développements méthodologiques pour la préparation de composés à visée anticancéreuse. : accès à des analogues du TMC-95A et synthèse totale de la Spisulosine et de son analogue fluoré : Synthetic methods for the preparation of new anti-cancer compounds : acces to new TMC-95A analogs and total synthesis of Spisulosine and its fluoro analog.” 2011. Web. 04 Dec 2020.

Vancouver:

Malik G. Développements méthodologiques pour la préparation de composés à visée anticancéreuse. : accès à des analogues du TMC-95A et synthèse totale de la Spisulosine et de son analogue fluoré : Synthetic methods for the preparation of new anti-cancer compounds : acces to new TMC-95A analogs and total synthesis of Spisulosine and its fluoro analog. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2011. [cited 2020 Dec 04]. Available from: http://www.theses.fr/2011PA112250.

Council of Science Editors:

Malik G. Développements méthodologiques pour la préparation de composés à visée anticancéreuse. : accès à des analogues du TMC-95A et synthèse totale de la Spisulosine et de son analogue fluoré : Synthetic methods for the preparation of new anti-cancer compounds : acces to new TMC-95A analogs and total synthesis of Spisulosine and its fluoro analog. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2011. Available from: http://www.theses.fr/2011PA112250

13. Cheviet, Thomas. Ciblage d'enzymes du métabolisme purique chez Plasmodium falciparum : Conception et étude de molécules bioactives : Targeting purine metabolizing enzymes from Plasmodium falciparum : Design and Study of bio-actives derivatives.

Degree: Docteur es, Ingénierie Biomoléculaire, 2019, Montpellier

Le paludisme, problème de santé publique mondial, est dû à plusieurs parasites possédant la caractéristique de n'avoir qu'une voie de biosynthèse nucléotidique : la voie… (more)

Subjects/Keywords: Chimie médicinale; Chimie du phosphore; Analogues nucléotidiques; Plasmodium falciparum; Analyses de biomolécules; Aziridines; Medicinal chemistry; Phosphorus chemistry; Nucleotides derivatives; Plasmodium falciparum; Biomolecules analysis; Aziridines

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

APA (6th Edition):

Cheviet, T. (2019). Ciblage d'enzymes du métabolisme purique chez Plasmodium falciparum : Conception et étude de molécules bioactives : Targeting purine metabolizing enzymes from Plasmodium falciparum : Design and Study of bio-actives derivatives. (Doctoral Dissertation). Montpellier. Retrieved from http://www.theses.fr/2019MONTS121

Chicago Manual of Style (16th Edition):

Cheviet, Thomas. “Ciblage d'enzymes du métabolisme purique chez Plasmodium falciparum : Conception et étude de molécules bioactives : Targeting purine metabolizing enzymes from Plasmodium falciparum : Design and Study of bio-actives derivatives.” 2019. Doctoral Dissertation, Montpellier. Accessed December 04, 2020. http://www.theses.fr/2019MONTS121.

MLA Handbook (7th Edition):

Cheviet, Thomas. “Ciblage d'enzymes du métabolisme purique chez Plasmodium falciparum : Conception et étude de molécules bioactives : Targeting purine metabolizing enzymes from Plasmodium falciparum : Design and Study of bio-actives derivatives.” 2019. Web. 04 Dec 2020.

Vancouver:

Cheviet T. Ciblage d'enzymes du métabolisme purique chez Plasmodium falciparum : Conception et étude de molécules bioactives : Targeting purine metabolizing enzymes from Plasmodium falciparum : Design and Study of bio-actives derivatives. [Internet] [Doctoral dissertation]. Montpellier; 2019. [cited 2020 Dec 04]. Available from: http://www.theses.fr/2019MONTS121.

Council of Science Editors:

Cheviet T. Ciblage d'enzymes du métabolisme purique chez Plasmodium falciparum : Conception et étude de molécules bioactives : Targeting purine metabolizing enzymes from Plasmodium falciparum : Design and Study of bio-actives derivatives. [Doctoral Dissertation]. Montpellier; 2019. Available from: http://www.theses.fr/2019MONTS121

14. Bochatay, Valentin. Allénylsilanes, allénylzincs et allénylboranes : préparation stéréosélective à partir d'électrophiles propargyliques et étude de réactivité : Allenylsilanes, allenylzincs and allenylboranes : stereoselective synthesis from propargylic electrophiles and study of their reactivity.

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

Cette thèse a été consacrée à la formation et l'utilisation de 4-amino- et 4-hydroxy-1-allénylmétaux. Deux méthodes de préparation stéréosélective et stéréospécifique des 4-sulfinamido- et 4-acétamido-1-allénylsilanes… (more)

Subjects/Keywords: Allénylzincs; Allénylsilanes; Allénylboranes; Silylzincation; Fluorodésilylation électrophile; Borylcupration; Acetylenic aziridines; Acetylenic epoxides; Borylcupration; 547

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APA (6th Edition):

Bochatay, V. (2016). Allénylsilanes, allénylzincs et allénylboranes : préparation stéréosélective à partir d'électrophiles propargyliques et étude de réactivité : Allenylsilanes, allenylzincs and allenylboranes : stereoselective synthesis from propargylic electrophiles and study of their reactivity. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2016PA066288

Chicago Manual of Style (16th Edition):

Bochatay, Valentin. “Allénylsilanes, allénylzincs et allénylboranes : préparation stéréosélective à partir d'électrophiles propargyliques et étude de réactivité : Allenylsilanes, allenylzincs and allenylboranes : stereoselective synthesis from propargylic electrophiles and study of their reactivity.” 2016. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed December 04, 2020. http://www.theses.fr/2016PA066288.

MLA Handbook (7th Edition):

Bochatay, Valentin. “Allénylsilanes, allénylzincs et allénylboranes : préparation stéréosélective à partir d'électrophiles propargyliques et étude de réactivité : Allenylsilanes, allenylzincs and allenylboranes : stereoselective synthesis from propargylic electrophiles and study of their reactivity.” 2016. Web. 04 Dec 2020.

Vancouver:

Bochatay V. Allénylsilanes, allénylzincs et allénylboranes : préparation stéréosélective à partir d'électrophiles propargyliques et étude de réactivité : Allenylsilanes, allenylzincs and allenylboranes : stereoselective synthesis from propargylic electrophiles and study of their reactivity. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2016. [cited 2020 Dec 04]. Available from: http://www.theses.fr/2016PA066288.

Council of Science Editors:

Bochatay V. Allénylsilanes, allénylzincs et allénylboranes : préparation stéréosélective à partir d'électrophiles propargyliques et étude de réactivité : Allenylsilanes, allenylzincs and allenylboranes : stereoselective synthesis from propargylic electrophiles and study of their reactivity. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2016. Available from: http://www.theses.fr/2016PA066288

15. A. Tamburrini. ONE-POT SYNTHESIS OF THIO-GLYCOMIMETICS THROUGH RING OPENING REACTIONS.

Degree: 2019, Università degli Studi di Milano

 Glycomimetics are compounds able to mimic structural and functional aspects of the corresponding natural carbohydrates. The main goal of using these mimetics, e.g. as therapeutic… (more)

Subjects/Keywords: Glycomimetics; DC-SIGN; one-pot reaction; carbohydrates; aziridines; Settore CHIM/06 - Chimica Organica

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APA (6th Edition):

Tamburrini, A. (2019). ONE-POT SYNTHESIS OF THIO-GLYCOMIMETICS THROUGH RING OPENING REACTIONS. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/607912

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):

Tamburrini, A.. “ONE-POT SYNTHESIS OF THIO-GLYCOMIMETICS THROUGH RING OPENING REACTIONS.” 2019. Thesis, Università degli Studi di Milano. Accessed December 04, 2020. http://hdl.handle.net/2434/607912.

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

MLA Handbook (7th Edition):

Tamburrini, A.. “ONE-POT SYNTHESIS OF THIO-GLYCOMIMETICS THROUGH RING OPENING REACTIONS.” 2019. Web. 04 Dec 2020.

Vancouver:

Tamburrini A. ONE-POT SYNTHESIS OF THIO-GLYCOMIMETICS THROUGH RING OPENING REACTIONS. [Internet] [Thesis]. Università degli Studi di Milano; 2019. [cited 2020 Dec 04]. Available from: http://hdl.handle.net/2434/607912.

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

Council of Science Editors:

Tamburrini A. ONE-POT SYNTHESIS OF THIO-GLYCOMIMETICS THROUGH RING OPENING REACTIONS. [Thesis]. Università degli Studi di Milano; 2019. Available from: http://hdl.handle.net/2434/607912

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


Michigan State University

16. Salehi Marzijarani, Nastaran. I. Catalytic asymmetric halofunctionalization of olefins : reaction discovery and mechanistic studies ; II. Development of new transformations for further modification of aziridines.

Degree: 2016, Michigan State University

Thesis Ph. D. Michigan State University. Chemistry 2016

My doctorate research work with Professor Borhan has focused on various aspects of synthetic, mechanistic and physical… (more)

Subjects/Keywords: Alkenes; Aziridines; Piperidine; Chemistry; Halenium affinity scale; Pyrrolidine; Chlorocyclization; Diastereoselective halofunctionalization reactions; Enantioselective halofunctionalization reactions

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APA (6th Edition):

Salehi Marzijarani, N. (2016). I. Catalytic asymmetric halofunctionalization of olefins : reaction discovery and mechanistic studies ; II. Development of new transformations for further modification of aziridines. (Thesis). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:4043

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):

Salehi Marzijarani, Nastaran. “I. Catalytic asymmetric halofunctionalization of olefins : reaction discovery and mechanistic studies ; II. Development of new transformations for further modification of aziridines.” 2016. Thesis, Michigan State University. Accessed December 04, 2020. http://etd.lib.msu.edu/islandora/object/etd:4043.

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

MLA Handbook (7th Edition):

Salehi Marzijarani, Nastaran. “I. Catalytic asymmetric halofunctionalization of olefins : reaction discovery and mechanistic studies ; II. Development of new transformations for further modification of aziridines.” 2016. Web. 04 Dec 2020.

Vancouver:

Salehi Marzijarani N. I. Catalytic asymmetric halofunctionalization of olefins : reaction discovery and mechanistic studies ; II. Development of new transformations for further modification of aziridines. [Internet] [Thesis]. Michigan State University; 2016. [cited 2020 Dec 04]. Available from: http://etd.lib.msu.edu/islandora/object/etd:4043.

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

Council of Science Editors:

Salehi Marzijarani N. I. Catalytic asymmetric halofunctionalization of olefins : reaction discovery and mechanistic studies ; II. Development of new transformations for further modification of aziridines. [Thesis]. Michigan State University; 2016. Available from: http://etd.lib.msu.edu/islandora/object/etd:4043

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

17. 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 04, 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. 04 Dec 2020.

Vancouver:

Semina E. Synthesis of new cyclic and acyclic biologically relevant amino acid derivatives. [Internet] [Thesis]. Ghent University; 2016. [cited 2020 Dec 04]. 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

18. Toledo, Fabiano Travanca. Síntese e aplicação sintética de compostos orgânicos de selênio e telúrio.

Degree: PhD, Química Orgânica, 2010, University of São Paulo

Nesta tese foram desenvolvidas metodologias sintéticas para a abertura de N-tosilaziridinas, provenientes de aminoácidos, via arilcianocupratos de ordem superior, os quais foram gerados pela reação… (more)

Subjects/Keywords: Arinos; Aryl tellurides; Arynes; Aziridinas; Aziridines; Cianocupratos de ordem superior; High order cyanocuprates; Tellurium amines; Teluretos arílicos; Teluretos nitrogenados

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APA (6th Edition):

Toledo, F. T. (2010). Síntese e aplicação sintética de compostos orgânicos de selênio e telúrio. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/46/46135/tde-10112010-101057/ ;

Chicago Manual of Style (16th Edition):

Toledo, Fabiano Travanca. “Síntese e aplicação sintética de compostos orgânicos de selênio e telúrio.” 2010. Doctoral Dissertation, University of São Paulo. Accessed December 04, 2020. http://www.teses.usp.br/teses/disponiveis/46/46135/tde-10112010-101057/ ;.

MLA Handbook (7th Edition):

Toledo, Fabiano Travanca. “Síntese e aplicação sintética de compostos orgânicos de selênio e telúrio.” 2010. Web. 04 Dec 2020.

Vancouver:

Toledo FT. Síntese e aplicação sintética de compostos orgânicos de selênio e telúrio. [Internet] [Doctoral dissertation]. University of São Paulo; 2010. [cited 2020 Dec 04]. Available from: http://www.teses.usp.br/teses/disponiveis/46/46135/tde-10112010-101057/ ;.

Council of Science Editors:

Toledo FT. Síntese e aplicação sintética de compostos orgânicos de selênio e telúrio. [Doctoral Dissertation]. University of São Paulo; 2010. Available from: http://www.teses.usp.br/teses/disponiveis/46/46135/tde-10112010-101057/ ;


Indian Institute of Science

19. Gopinath, P. Synthesis Of Novel Chalcogenides Using Acyloxyphosphonium Intermediates And Doubly Activated Cyclopropanes.

Degree: PhD, Faculty of Science, 2013, Indian Institute of Science

 The thesis entitled "Synthesis of Novel Chalcogenides using Acyloxyphosphonium Intermediates and Doubly Activated Cyclopropanes" is divided into six chapters. Chapter 1: Part 1: Synthesis of… (more)

Subjects/Keywords: Cyclopropanes; Chalcogenides - Synthesis; Acyloxyphosphonium; Thioesters; Bromo Esters; Bromo Thioesters; Benzyltriethylammonium Tetrathiomolybdate; Dihydrothiophenes; Thiophenes; Selenolates; Aziridines; Epoxides; Thioaroylate; Organic Chemistry

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APA (6th Edition):

Gopinath, P. (2013). Synthesis Of Novel Chalcogenides Using Acyloxyphosphonium Intermediates And Doubly Activated Cyclopropanes. (Doctoral Dissertation). Indian Institute of Science. Retrieved from http://etd.iisc.ac.in/handle/2005/2157

Chicago Manual of Style (16th Edition):

Gopinath, P. “Synthesis Of Novel Chalcogenides Using Acyloxyphosphonium Intermediates And Doubly Activated Cyclopropanes.” 2013. Doctoral Dissertation, Indian Institute of Science. Accessed December 04, 2020. http://etd.iisc.ac.in/handle/2005/2157.

MLA Handbook (7th Edition):

Gopinath, P. “Synthesis Of Novel Chalcogenides Using Acyloxyphosphonium Intermediates And Doubly Activated Cyclopropanes.” 2013. Web. 04 Dec 2020.

Vancouver:

Gopinath P. Synthesis Of Novel Chalcogenides Using Acyloxyphosphonium Intermediates And Doubly Activated Cyclopropanes. [Internet] [Doctoral dissertation]. Indian Institute of Science; 2013. [cited 2020 Dec 04]. Available from: http://etd.iisc.ac.in/handle/2005/2157.

Council of Science Editors:

Gopinath P. Synthesis Of Novel Chalcogenides Using Acyloxyphosphonium Intermediates And Doubly Activated Cyclopropanes. [Doctoral Dissertation]. Indian Institute of Science; 2013. Available from: http://etd.iisc.ac.in/handle/2005/2157

20. D.M. Carminati. METAL PORPHYRIN COMPLEXES: SMART CATALYSTS TO PROMOTE ECO-FRIENDLY C-C AND C-N BOND FORMATIONS.

Degree: 2018, Università degli Studi di Milano

 Cyclopropanes and nitrogen-containing compounds, such as aziridines, indoles and amines, are interesting molecules from a synthetic point of view because they are often used as… (more)

Subjects/Keywords: porphyrin; metal porphyrin complexes; catalysis; cyclopropanes; aziridines; oxazolidinones; indoles; amines; Settore CHIM/03 - Chimica Generale e Inorganica

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APA (6th Edition):

Carminati, D. (2018). METAL PORPHYRIN COMPLEXES: SMART CATALYSTS TO PROMOTE ECO-FRIENDLY C-C AND C-N BOND FORMATIONS. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/541869

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):

Carminati, D.M.. “METAL PORPHYRIN COMPLEXES: SMART CATALYSTS TO PROMOTE ECO-FRIENDLY C-C AND C-N BOND FORMATIONS.” 2018. Thesis, Università degli Studi di Milano. Accessed December 04, 2020. http://hdl.handle.net/2434/541869.

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

MLA Handbook (7th Edition):

Carminati, D.M.. “METAL PORPHYRIN COMPLEXES: SMART CATALYSTS TO PROMOTE ECO-FRIENDLY C-C AND C-N BOND FORMATIONS.” 2018. Web. 04 Dec 2020.

Vancouver:

Carminati D. METAL PORPHYRIN COMPLEXES: SMART CATALYSTS TO PROMOTE ECO-FRIENDLY C-C AND C-N BOND FORMATIONS. [Internet] [Thesis]. Università degli Studi di Milano; 2018. [cited 2020 Dec 04]. Available from: http://hdl.handle.net/2434/541869.

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

Council of Science Editors:

Carminati D. METAL PORPHYRIN COMPLEXES: SMART CATALYSTS TO PROMOTE ECO-FRIENDLY C-C AND C-N BOND FORMATIONS. [Thesis]. Università degli Studi di Milano; 2018. Available from: http://hdl.handle.net/2434/541869

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


Universitat de Barcelona

21. Alcaide López, Anna. A modular approach to sphingolipid analogs mediated by aziridines: Synthesis and biological studies.

Degree: Departament de Farmacologia i Química Terapèutica, 2012, Universitat de Barcelona

 Los esfingolípidos (SL) son biomoléculas esenciales para las funciones fisiológicas de las células. El metabolismo anómalo o la expresión de SL específicos o glicoesfingolípidos (GSL)… (more)

Subjects/Keywords: Síntesi de fàrmacs; Síntesis de fármacos; Drug synthesis; Sphingolipids; Esfingolípidos (SL); Esfingolípids; Aziridinas; Aziridines; Ciències de la Salut; 615

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APA (6th Edition):

Alcaide López, A. (2012). A modular approach to sphingolipid analogs mediated by aziridines: Synthesis and biological studies. (Thesis). Universitat de Barcelona. Retrieved from http://hdl.handle.net/10803/96979

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):

Alcaide López, Anna. “A modular approach to sphingolipid analogs mediated by aziridines: Synthesis and biological studies.” 2012. Thesis, Universitat de Barcelona. Accessed December 04, 2020. http://hdl.handle.net/10803/96979.

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

MLA Handbook (7th Edition):

Alcaide López, Anna. “A modular approach to sphingolipid analogs mediated by aziridines: Synthesis and biological studies.” 2012. Web. 04 Dec 2020.

Vancouver:

Alcaide López A. A modular approach to sphingolipid analogs mediated by aziridines: Synthesis and biological studies. [Internet] [Thesis]. Universitat de Barcelona; 2012. [cited 2020 Dec 04]. Available from: http://hdl.handle.net/10803/96979.

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

Council of Science Editors:

Alcaide López A. A modular approach to sphingolipid analogs mediated by aziridines: Synthesis and biological studies. [Thesis]. Universitat de Barcelona; 2012. Available from: http://hdl.handle.net/10803/96979

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


University of Oxford

22. Feast, George C. Aziridinations of tethered allenes.

Degree: PhD, 2011, University of Oxford

 This thesis describes the synthesis and reactivity of previously unprecedented bicyclic methylene aziridines via rhodium(II) catalysed cyclisation of α-allenic N-tosyloxycarbamates. These aziridines undergo reaction with… (more)

Subjects/Keywords: 547.59; Organic chemistry; Organic synthesis; Physical Sciences; Chemistry & allied sciences; Synthetic organic chemistry; Organometallic Chemistry; aziridines; allenes; rhodium; carbamates; sulfamates

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APA (6th Edition):

Feast, G. C. (2011). Aziridinations of tethered allenes. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:9b7b1fa7-c2fd-4cf1-94f8-333504332d7d ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.558554

Chicago Manual of Style (16th Edition):

Feast, George C. “Aziridinations of tethered allenes.” 2011. Doctoral Dissertation, University of Oxford. Accessed December 04, 2020. http://ora.ox.ac.uk/objects/uuid:9b7b1fa7-c2fd-4cf1-94f8-333504332d7d ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.558554.

MLA Handbook (7th Edition):

Feast, George C. “Aziridinations of tethered allenes.” 2011. Web. 04 Dec 2020.

Vancouver:

Feast GC. Aziridinations of tethered allenes. [Internet] [Doctoral dissertation]. University of Oxford; 2011. [cited 2020 Dec 04]. Available from: http://ora.ox.ac.uk/objects/uuid:9b7b1fa7-c2fd-4cf1-94f8-333504332d7d ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.558554.

Council of Science Editors:

Feast GC. Aziridinations of tethered allenes. [Doctoral Dissertation]. University of Oxford; 2011. Available from: http://ora.ox.ac.uk/objects/uuid:9b7b1fa7-c2fd-4cf1-94f8-333504332d7d ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.558554


University of Bradford

23. Garelnabi, Elrashied Ali Elobaid. New applications of imidazotetrazinone prodrugs : synthesis and mechanistic investigation of novel imidazotetrazinones as prodrugs of aziridines and as traceless carriers for drug delivery to the central nervous system.

Degree: PhD, 2010, University of Bradford

 New imidazotetrazinones have been synthesised that possess features in their structures to release aziridinium ions upon ring opening. Unstable 2-aminoethylisocyanates were required in this preparation,… (more)

Subjects/Keywords: 616.99; Imidazotetrazinone prodrugs; Synthesis; Aziridinium ions; Aziridines; Drug delivery

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

APA (6th Edition):

Garelnabi, E. A. E. (2010). New applications of imidazotetrazinone prodrugs : synthesis and mechanistic investigation of novel imidazotetrazinones as prodrugs of aziridines and as traceless carriers for drug delivery to the central nervous system. (Doctoral Dissertation). University of Bradford. Retrieved from http://hdl.handle.net/10454/4418

Chicago Manual of Style (16th Edition):

Garelnabi, Elrashied Ali Elobaid. “New applications of imidazotetrazinone prodrugs : synthesis and mechanistic investigation of novel imidazotetrazinones as prodrugs of aziridines and as traceless carriers for drug delivery to the central nervous system.” 2010. Doctoral Dissertation, University of Bradford. Accessed December 04, 2020. http://hdl.handle.net/10454/4418.

MLA Handbook (7th Edition):

Garelnabi, Elrashied Ali Elobaid. “New applications of imidazotetrazinone prodrugs : synthesis and mechanistic investigation of novel imidazotetrazinones as prodrugs of aziridines and as traceless carriers for drug delivery to the central nervous system.” 2010. Web. 04 Dec 2020.

Vancouver:

Garelnabi EAE. New applications of imidazotetrazinone prodrugs : synthesis and mechanistic investigation of novel imidazotetrazinones as prodrugs of aziridines and as traceless carriers for drug delivery to the central nervous system. [Internet] [Doctoral dissertation]. University of Bradford; 2010. [cited 2020 Dec 04]. Available from: http://hdl.handle.net/10454/4418.

Council of Science Editors:

Garelnabi EAE. New applications of imidazotetrazinone prodrugs : synthesis and mechanistic investigation of novel imidazotetrazinones as prodrugs of aziridines and as traceless carriers for drug delivery to the central nervous system. [Doctoral Dissertation]. University of Bradford; 2010. Available from: http://hdl.handle.net/10454/4418


The Ohio State University

24. Lapinsky, David J. STUDIES IN AZIRIDINE-ALLYLSILANE CHEMISTRY: EXTENSION OF SCOPE.

Degree: PhD, Pharmacy, 2002, The Ohio State University

 We have been interested in developing methodology for the synthesis of alkaloids and other heterocycles that could serve as potential drug candidates. In this regard,… (more)

Subjects/Keywords: Chemistry, Pharmaceutical; aziridines; allylsilanes; nitrogen heterocycles; bicyclic heterocyclic compounds

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

APA (6th Edition):

Lapinsky, D. J. (2002). STUDIES IN AZIRIDINE-ALLYLSILANE CHEMISTRY: EXTENSION OF SCOPE. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1038954949

Chicago Manual of Style (16th Edition):

Lapinsky, David J. “STUDIES IN AZIRIDINE-ALLYLSILANE CHEMISTRY: EXTENSION OF SCOPE.” 2002. Doctoral Dissertation, The Ohio State University. Accessed December 04, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1038954949.

MLA Handbook (7th Edition):

Lapinsky, David J. “STUDIES IN AZIRIDINE-ALLYLSILANE CHEMISTRY: EXTENSION OF SCOPE.” 2002. Web. 04 Dec 2020.

Vancouver:

Lapinsky DJ. STUDIES IN AZIRIDINE-ALLYLSILANE CHEMISTRY: EXTENSION OF SCOPE. [Internet] [Doctoral dissertation]. The Ohio State University; 2002. [cited 2020 Dec 04]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1038954949.

Council of Science Editors:

Lapinsky DJ. STUDIES IN AZIRIDINE-ALLYLSILANE CHEMISTRY: EXTENSION OF SCOPE. [Doctoral Dissertation]. The Ohio State University; 2002. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1038954949


University of Cincinnati

25. HANCOCK, MATTHEW THOMAS. THE DEVELOPMENT OF NOVEL AND CONVENIENT TRANSFORMATIONS OF AZIRIDINES.

Degree: PhD, Arts and Sciences : Chemistry, 2003, University of Cincinnati

 Several novel transformations of aziridines to 1,2-diamines, 2-oxazolidinones, and benzodiazepines have been developed. Previous work in the Pinhas group showed that an aziridine could be… (more)

Subjects/Keywords: Chemistry, Organic; aziridines; diamines; oxazolidinones; benzodiazepines; carbon dioxide insertion

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APA (6th Edition):

HANCOCK, M. T. (2003). THE DEVELOPMENT OF NOVEL AND CONVENIENT TRANSFORMATIONS OF AZIRIDINES. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1054137190

Chicago Manual of Style (16th Edition):

HANCOCK, MATTHEW THOMAS. “THE DEVELOPMENT OF NOVEL AND CONVENIENT TRANSFORMATIONS OF AZIRIDINES.” 2003. Doctoral Dissertation, University of Cincinnati. Accessed December 04, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1054137190.

MLA Handbook (7th Edition):

HANCOCK, MATTHEW THOMAS. “THE DEVELOPMENT OF NOVEL AND CONVENIENT TRANSFORMATIONS OF AZIRIDINES.” 2003. Web. 04 Dec 2020.

Vancouver:

HANCOCK MT. THE DEVELOPMENT OF NOVEL AND CONVENIENT TRANSFORMATIONS OF AZIRIDINES. [Internet] [Doctoral dissertation]. University of Cincinnati; 2003. [cited 2020 Dec 04]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1054137190.

Council of Science Editors:

HANCOCK MT. THE DEVELOPMENT OF NOVEL AND CONVENIENT TRANSFORMATIONS OF AZIRIDINES. [Doctoral Dissertation]. University of Cincinnati; 2003. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1054137190


Université Montpellier II

26. Kasthuri, Mahesh. Nouveaux anti-viraux pour le traitement des affections associées aux virus émergents : New antiviral for the treatment of the infections associated with the emergent viruses.

Degree: Docteur es, Ingénérie Moléculaire, 2011, Université Montpellier II

Dans un premier chapitre, nous avons présenté un historique succinct de la chimiothérapie antivirale et l'utilisation d'analogues nucléos(t)idiques. Nous nous sommes focalisés en particulier sur… (more)

Subjects/Keywords: Anti-viraux; Virus émergents; Nucléotides; Nucleosides phosphonate acyclique; Dedoublement; Ouverture du cycle des azirines et aziridines; Antiviral; Emergent viruses; Nucleotides; Acyclic nucleoside phosphonates; Chiral resolution; Ring opening of azirine and aziridines

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APA (6th Edition):

Kasthuri, M. (2011). Nouveaux anti-viraux pour le traitement des affections associées aux virus émergents : New antiviral for the treatment of the infections associated with the emergent viruses. (Doctoral Dissertation). Université Montpellier II. Retrieved from http://www.theses.fr/2011MON20085

Chicago Manual of Style (16th Edition):

Kasthuri, Mahesh. “Nouveaux anti-viraux pour le traitement des affections associées aux virus émergents : New antiviral for the treatment of the infections associated with the emergent viruses.” 2011. Doctoral Dissertation, Université Montpellier II. Accessed December 04, 2020. http://www.theses.fr/2011MON20085.

MLA Handbook (7th Edition):

Kasthuri, Mahesh. “Nouveaux anti-viraux pour le traitement des affections associées aux virus émergents : New antiviral for the treatment of the infections associated with the emergent viruses.” 2011. Web. 04 Dec 2020.

Vancouver:

Kasthuri M. Nouveaux anti-viraux pour le traitement des affections associées aux virus émergents : New antiviral for the treatment of the infections associated with the emergent viruses. [Internet] [Doctoral dissertation]. Université Montpellier II; 2011. [cited 2020 Dec 04]. Available from: http://www.theses.fr/2011MON20085.

Council of Science Editors:

Kasthuri M. Nouveaux anti-viraux pour le traitement des affections associées aux virus émergents : New antiviral for the treatment of the infections associated with the emergent viruses. [Doctoral Dissertation]. Université Montpellier II; 2011. Available from: http://www.theses.fr/2011MON20085


University of Florida

27. Schilling, Stefan, 1974-. Chemoenzymatic synthesis and utility of vinyl aziridines an approach to the synthesis of (+)-7-deoxypancratistatin and the preparation of several truncated analogs.

Degree: PhD, Chemistry, 2001, University of Florida

Subjects/Keywords: Acetates; Alcohols; Alkaloids; Alkenes; Aziridines; Epoxy compounds; Ethers; Lactones; Oxidation; Tetrahedrons; Aziridines; Heterocyclic compounds  – Synthesis

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APA (6th Edition):

Schilling, Stefan, 1. (2001). Chemoenzymatic synthesis and utility of vinyl aziridines an approach to the synthesis of (+)-7-deoxypancratistatin and the preparation of several truncated analogs. (Doctoral Dissertation). University of Florida. Retrieved from https://ufdc.ufl.edu/AA00038644

Chicago Manual of Style (16th Edition):

Schilling, Stefan, 1974-. “Chemoenzymatic synthesis and utility of vinyl aziridines an approach to the synthesis of (+)-7-deoxypancratistatin and the preparation of several truncated analogs.” 2001. Doctoral Dissertation, University of Florida. Accessed December 04, 2020. https://ufdc.ufl.edu/AA00038644.

MLA Handbook (7th Edition):

Schilling, Stefan, 1974-. “Chemoenzymatic synthesis and utility of vinyl aziridines an approach to the synthesis of (+)-7-deoxypancratistatin and the preparation of several truncated analogs.” 2001. Web. 04 Dec 2020.

Vancouver:

Schilling, Stefan 1. Chemoenzymatic synthesis and utility of vinyl aziridines an approach to the synthesis of (+)-7-deoxypancratistatin and the preparation of several truncated analogs. [Internet] [Doctoral dissertation]. University of Florida; 2001. [cited 2020 Dec 04]. Available from: https://ufdc.ufl.edu/AA00038644.

Council of Science Editors:

Schilling, Stefan 1. Chemoenzymatic synthesis and utility of vinyl aziridines an approach to the synthesis of (+)-7-deoxypancratistatin and the preparation of several truncated analogs. [Doctoral Dissertation]. University of Florida; 2001. Available from: https://ufdc.ufl.edu/AA00038644

28. 羽下, 豊和. Mechanistic Approaches to Asymmetric Synthesis of Aziridines from Guanidinium Ylides and Aryl Aldehydes : グアニジニウムイリド及び芳香族アルデヒドからの不斉アジリジン合成への機構的アプローチ.

Degree: Chiba University / 千葉大学

研究科: 千葉大学大学院医学薬学府

学位:千大院医薬博甲第薬29号

Subjects/Keywords: Guanidinium Ylides; Aziridines; Mechanism; グアニジニウムイリド; アジリジン; 反応機構

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APA (6th Edition):

羽下, . (n.d.). Mechanistic Approaches to Asymmetric Synthesis of Aziridines from Guanidinium Ylides and Aryl Aldehydes : グアニジニウムイリド及び芳香族アルデヒドからの不斉アジリジン合成への機構的アプローチ. (Thesis). Chiba University / 千葉大学. Retrieved from http://opac.ll.chiba-u.jp/da/curator/900022542/

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

羽下, 豊和. “Mechanistic Approaches to Asymmetric Synthesis of Aziridines from Guanidinium Ylides and Aryl Aldehydes : グアニジニウムイリド及び芳香族アルデヒドからの不斉アジリジン合成への機構的アプローチ.” Thesis, Chiba University / 千葉大学. Accessed December 04, 2020. http://opac.ll.chiba-u.jp/da/curator/900022542/.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

羽下, 豊和. “Mechanistic Approaches to Asymmetric Synthesis of Aziridines from Guanidinium Ylides and Aryl Aldehydes : グアニジニウムイリド及び芳香族アルデヒドからの不斉アジリジン合成への機構的アプローチ.” Web. 04 Dec 2020.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

羽下 . Mechanistic Approaches to Asymmetric Synthesis of Aziridines from Guanidinium Ylides and Aryl Aldehydes : グアニジニウムイリド及び芳香族アルデヒドからの不斉アジリジン合成への機構的アプローチ. [Internet] [Thesis]. Chiba University / 千葉大学; [cited 2020 Dec 04]. Available from: http://opac.ll.chiba-u.jp/da/curator/900022542/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

羽下 . Mechanistic Approaches to Asymmetric Synthesis of Aziridines from Guanidinium Ylides and Aryl Aldehydes : グアニジニウムイリド及び芳香族アルデヒドからの不斉アジリジン合成への機構的アプローチ. [Thesis]. Chiba University / 千葉大学; Available from: http://opac.ll.chiba-u.jp/da/curator/900022542/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.


Vanderbilt University

29. Mathew, Priya Ann. Progress Towards the Total Synthesis of Mitomycin C.

Degree: PhD, Chemistry, 2012, Vanderbilt University

 Mitomycin C is a clinically used antitumor natural product isolated from <i>Streptomyces caespitosus</i>. The biological activity and synthetic challenge of mitomycin C has generated broad… (more)

Subjects/Keywords: diastereoselective synthesis of complex polycyclic aziridines; advanced intermediates to mitomycin C; convergent synthesis of mitomycin C; spiroketal formation; aminoquinone; halonium promoted alkynyl amine cyclization

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APA (6th Edition):

Mathew, P. A. (2012). Progress Towards the Total Synthesis of Mitomycin C. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/13317

Chicago Manual of Style (16th Edition):

Mathew, Priya Ann. “Progress Towards the Total Synthesis of Mitomycin C.” 2012. Doctoral Dissertation, Vanderbilt University. Accessed December 04, 2020. http://hdl.handle.net/1803/13317.

MLA Handbook (7th Edition):

Mathew, Priya Ann. “Progress Towards the Total Synthesis of Mitomycin C.” 2012. Web. 04 Dec 2020.

Vancouver:

Mathew PA. Progress Towards the Total Synthesis of Mitomycin C. [Internet] [Doctoral dissertation]. Vanderbilt University; 2012. [cited 2020 Dec 04]. Available from: http://hdl.handle.net/1803/13317.

Council of Science Editors:

Mathew PA. Progress Towards the Total Synthesis of Mitomycin C. [Doctoral Dissertation]. Vanderbilt University; 2012. Available from: http://hdl.handle.net/1803/13317


Brigham Young University

30. Liu, Renmao. Asymmetric Dihydroxylation and Aziridination of Allenes and Related Chemistry.

Degree: PhD, 2007, Brigham Young University

 A novel method for asymmetric synthesis of α-hydroxy ketone with excellent regio- and stereoselectivity has been established by the systematic investigation of asymmetric dihydroxylation of… (more)

Subjects/Keywords: asymmetric dihydroxylation; aziridination; allenes; alkenes; α-hydroxy ketone; aziridines; Biochemistry; Chemistry

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APA (6th Edition):

Liu, R. (2007). Asymmetric Dihydroxylation and Aziridination of Allenes and Related Chemistry. (Doctoral Dissertation). Brigham Young University. Retrieved from https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=1898&context=etd

Chicago Manual of Style (16th Edition):

Liu, Renmao. “Asymmetric Dihydroxylation and Aziridination of Allenes and Related Chemistry.” 2007. Doctoral Dissertation, Brigham Young University. Accessed December 04, 2020. https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=1898&context=etd.

MLA Handbook (7th Edition):

Liu, Renmao. “Asymmetric Dihydroxylation and Aziridination of Allenes and Related Chemistry.” 2007. Web. 04 Dec 2020.

Vancouver:

Liu R. Asymmetric Dihydroxylation and Aziridination of Allenes and Related Chemistry. [Internet] [Doctoral dissertation]. Brigham Young University; 2007. [cited 2020 Dec 04]. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=1898&context=etd.

Council of Science Editors:

Liu R. Asymmetric Dihydroxylation and Aziridination of Allenes and Related Chemistry. [Doctoral Dissertation]. Brigham Young University; 2007. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=1898&context=etd

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