130625-74-0Relevant academic research and scientific papers
A synthesis of (-)-tetrahydrolipstatin in which the relative stereochemistry is controlled by a phenyldimethylsilyl group
Fleming, Ian,Lawrence, Nicholas J.
, p. 3645 - 3648 (1990)
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).
