A synthesis of (−)-tetrahydrolipstatin in which the relative stereochemistry is controlled by a phenyldimethylsilyl group
作者:Ian Fleming、Nicholas J. Lawrence
DOI:10.1016/s0040-4039(00)94466-6
日期:1990.1
The alkylation ofa β-silylenolate and the hydroboration of an allylsilane successively control the relative stereochemistry of the three stereogenic centres on the carbon backbone in a synthesis of the esterase inhibitor tetrahydrolipstatin (21).