120393-35-3Relevant articles and documents
1,3-DIPOLAR CYCLOADDITION OF 2-BENZYLIDENEINDAN-1,3-DIONE α-OXIDE TO OLEFINS
Krysin, M. Yu.,Anokhina, I. K.,Zalukaev, L. P.
, p. 1166 - 1169 (2007/10/02)
A carbonyl ylid, which reacts with maleic anhydride, N-phenylmaleinimide, and β-nitrostyrene to form adducts resulting from 1,3-dipolar cycloaddition, is formed reversibly when 2-benzylideneindan-1,3-dione α-oxide is heated (80 deg C).The reaction proceeds regio- and stereospecifically.