135367-12-3Relevant academic research and scientific papers
Stereocontrolled preparation of tetrahydrofurans from acid-promoted rearrangements of allylic acetals
Hopkins, Mark H.,Overman, Larry E.,Rishton, Gilbert M.
, p. 5354 - 5365 (2007/10/02)
A new method for constructing substituted tetrahydrofurans from readily available allylic did and carbonyl components is reported (eq 1). This synthesis is highly stereocontrolled and allows carbon side chains to be incorporated at each carbon. Enantiomer
