515178-90-2Relevant academic research and scientific papers
A sequential stereocontrolled cyclopropane ring formation and semi-pinacol rearrangement
Marson, Charles M.,Oare, Catriona A.,McGregor, Jane,Walsgrove, Timothy,Grinter, Trevor J.,Adams, Harry
, p. 141 - 143 (2003)
Treatment of an unsaturated 2,3-epoxy alcohol with SnBr4 leads to a stereoselective formation of a cyclopropane ring, and an α-ketol unit as part of a subsequent ring expansion.
