252961-65-2Relevant academic research and scientific papers
Unusual stereochemical course of epoxide rearrangement in a carvone-derived series
Neef, Guenter,Baesler, Siegfried,Depke, Gisbert,Vierhufe, Harry
, p. 7969 - 7973 (2007/10/03)
Carvone-derived 2,3-epoxy alcohol derivatives rearrange with stereoselective formation of ring-contracted ketones. In contrast to previously described similar processes, the stereochemical result seems to be independent of epoxide configuration.
