DISPARITY IN THE TANDEM EPOXIDE ALLYLIC ALCOHOL [1,2] [2,3]-WITTIG REARRANGEMENT OF CIS-1-BENZYLOXY-3,4-EPOXYCYCLOPENTANE AND TRANS-1-BENZYLOXY-3,4-EPOXYCYCLOPENTANE/
Pc. Brookes et al., DISPARITY IN THE TANDEM EPOXIDE ALLYLIC ALCOHOL [1,2] [2,3]-WITTIG REARRANGEMENT OF CIS-1-BENZYLOXY-3,4-EPOXYCYCLOPENTANE AND TRANS-1-BENZYLOXY-3,4-EPOXYCYCLOPENTANE/, Journal of the Chemical Society. Perkin transactions. I (Print), (12), 1998, pp. 1899-1901
The influence of the relative stereochemistry of the epoxide and benzy
loxy functionalities present in cis-1 and trans-1-benzyloxy-3,4-epoxyc
yclopentane 3 on the tandem epoxide-allylic alcohol-[1,2]/[2,3]-Wittig
rearrangement has been studied, together with the Wittig rearrangemen
t of the intermediate alcohols 2 and 4.