1174507-66-4Relevant articles and documents
Facial selectivity and stereospecificity in the (4 + 3) cycloaddition of epoxy enol silanes
Lo, Brian,Chiu, Pauline
supporting information; experimental part, p. 864 - 867 (2011/05/06)
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