1268091-76-4Relevant academic research and scientific papers
Facial selectivity and stereospecificity in the (4 + 3) cycloaddition of epoxy enol silanes
Lo, Brian,Chiu, Pauline
, p. 864 - 867 (2011)
The scope of the (4 + 3) cycloaddition using epoxy enol silanes has been examined. Unhindered and nucleophilic dienes react to give the highest yields, but hindered dienes give rise to higher diastereoselectivities. Notably, the cycloaddition shows facial
