Tetrahedron Letters p. 8047 - 8050 (1993)
Update date:2022-08-04
Topics:
Kress, Michael H.
Kaller, Brian F.
Kishi, Yoshito
An efficient, stereoselective synthesis of an enantiomerically pure C-ring precursor 14-S of O-cinnamoyltaxicins-I and -II has been achieved from 3-methyl-2-cyclohexen-1-ol, using a <2,3> Wittig rearrangement as the key step.
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