1,3-Dipolar cycloaddition of 2-benzylideneindan-1,3-dione α-oxide to olefins

Autor: Krysin, M. Yu., Anokhina, I. K., Zalukaev, L. P.
Zdroj: Chemistry of Heterocyclic Compounds; November 1987, Vol. 23 Issue: 11 p1166-1169, 4p
Abstrakt: A carbonyl ylid, which reacts with maleic anhydride, N-phenylmaleinimide, and ?-nitrostyrene to form adducts resulting from 1,3-dipolar cycloaddition, is formed reversibly when 2-benzylideneindan-1,3-dione a-oxide is heated (80‡C). The reaction proceeds regio- and stereospecifically.
Databáze: Supplemental Index