Theoretical evidence on O–N type smiles rearrangement mechanism: a computational study on the intramolecular cyclization ofN-methyl-2-(2-chloropyridin-3-yloxy)-acetamide anion-Reference-Cited by-同舟云学术

Theoretical evidence on O–N type smiles rearrangement mechanism: a computational study on the intramolecular cyclization ofN-methyl-2-(2-chloropyridin-3-yloxy)-acetamide anion

Published:2008 Issue:3 Volume:21 Page:215-218
ISSN:0894-3230
Container-title:Journal of Physical Organic Chemistry
language:en
Short-container-title:J. Phys. Org. Chem.

Author:

Sun Hui,Li Jinghua,Zhang Dongju,Ma Chen,Liu Chengbu

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference29 articles.

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2. Oxazolines. XX. Synthesis of achiral and chiral thiiranes and olefins by reaction of carbonyl compounds with 2-(alkylthio)-2-oxazolines

3. A direct synthesis of olefins by reaction of carbonyl compounds with lithio derivatives of 2-[alkyl- or (2′-alkenyl)- or benzyl-sulfonyl]-benzothiazoles.

4. Synthesis of 2-Substituted-2,3- dihydro-1,4-dioxino[2,3-b]pyridine Derivatives

5. Smiles rearrangement for the synthesis of 5-amino-substituted [1]benzothieno[2,3- b ]pyridine

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