A DFT mechanistic study of the generation of azomethine ylides from the ring-opening reactions of stabilized aziridines and follow-up 1,3-dipolar cycloaddition reactions with acetaldehyde-Reference-Cited by-同舟云学术

A DFT mechanistic study of the generation of azomethine ylides from the ring-opening reactions of stabilized aziridines and follow-up 1,3-dipolar cycloaddition reactions with acetaldehyde

Published:2018-11 Issue: Volume:1144 Page:38-49
ISSN:2210-271X
Container-title:Computational and Theoretical Chemistry
language:en
Short-container-title:Computational and Theoretical Chemistry

Author:

Nantogma Shiraz^ORCID,Tia Richard,Adei Evans

Funder

National Council for Tertiary Education, Republic of Ghana

Teaching and Learning Innovation Fund

South Africa’s Centre for High Performance Computing

Publisher

Elsevier BV

Subject

Physical and Theoretical Chemistry,Condensed Matter Physics,Biochemistry

Reference34 articles.

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2. Intramolecular dipolar cycloaddition reactions with azomethine ylides;Coldham;J. Org. Chem.,1979

3. Evidence for an azomethine ylide intermediate in the carbonyl-assisted decarboxylation of sarcosine. A novel synthesis of dl-phenylephrine hydrochloride;Rizzi;J. Org. Chem.,1970

4. Generation of azomethine ylides via the desilylation reaction of immonium salts;Padwa;J. Org. Chem.,1984

5. Origin of the reactivity differences of substituted aziridines: CN vs CC bond breakages;Paasche;J. Org. Chem.,2009

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