130592-48-2Relevant articles and documents
The claisen rearrangement of 7-cinnamyloxy derivatives of noreugenin, 2-methylisoflavone and chrysin in quinoline
Andotra,Chawla,Jain
, p. 632 - 636 (2007/10/02)
7-Cinnamyloxy derivatives (2a, 2b, 2c) of noreugenin, 2-methylisoflavone and chrysin undergo Claisen rearrangement in refluxing quinoline to yield 8-(1-phenylprop-1-enyl) derivatives (3d, 3g, 3i respectively) and 4'-methyl-5'-phenylfuro[2',3':7,8] derivatives (4l, 4m, 4o respectively) as abnormal products. These have features similar to those of natural neoflavonoids.