ADDITION-REACTION OF PHOTOENOLS FROM O-METHYL-SUBSTITUTED AROMATIC KETONES WITH 5-ALKYLIDENE-1,3-DIOXANE-4,6-DIONE DERIVATIVES

Citation
T. Tsuno et K. Sugiyama, ADDITION-REACTION OF PHOTOENOLS FROM O-METHYL-SUBSTITUTED AROMATIC KETONES WITH 5-ALKYLIDENE-1,3-DIOXANE-4,6-DIONE DERIVATIVES, Heterocycles, 38(4), 1994, pp. 859-876
Citations number
65
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
03855414
Volume
38
Issue
4
Year of publication
1994
Pages
859 - 876
Database
ISI
SICI code
0385-5414(1994)38:4<859:AOPFOA>2.0.ZU;2-W
Abstract
Photolyses of 2-methylacetophenone or 2-methylbenzophenone with isobut ylidene Meldrum's acid or 5-isobutylidene-1,3-dioxane-4,6-dione deriva tives produced novel adducts, bonding between the beta-carbon of the a cylals and the 2-methyl carbon of the aromatic ketones. However, the p hotoenol derived from benzocyclobutenols by thermolysis did not underg o the addition reaction with the acylal. The benzocyclobutenols reacte d with isobutenylketene derived by pyrolysis of isobutylidene Meldrum' s acid to yield corresponding benzocyclobutenyl 4-methyl-3-pentenoate derivatives.