Reactions of 3, 5‐Dimethyl‐4‐Carbethoxy‐2‐Cyclohexen‐1‐One at α‐Position | Zendy

Rahman A. U. | Zendy; Khan M. Y. | Zendy

AI Assistant Blog Pricing

Home ZAIA Blog

Premium

Reactions of 3, 5‐Dimethyl‐4‐Carbethoxy‐2‐Cyclohexen‐1‐One at α‐Position

Author(s) -

Rahman A. U.,

Khan M. Y.

Publication year - 1984

Publication title -

journal of the chinese chemical society

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.329

H-Index - 45

eISSN - 2192-6549

pISSN - 0009-4536

DOI - 10.1002/jccs.198400023

Subject(s) - chemistry , knoevenagel condensation , alkylation , phenol , acylation , hydrolysis , dimethyl fumarate , organic chemistry , condensation , keto–enol tautomerism , medicinal chemistry , tautomer , catalysis , psychology , physics , psychiatry , multiple sclerosis , thermodynamics

3, 5‐Dimethyl‐4‐carbethoxy‐2‐cyclohexen‐1‐one has been synthesized through the Knoevenagel condensation 1 , which is then subjected to alkylation and acylation at α‐position. The resulting products are hydrolyzed and decarboxylated to α‐substituted cyclohexenones. 3, 5‐Dimethyl‐2‐cyclohexen‐1‐one is converted by N ‐bromosuccinimide to phenol via enolization 2 .

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research