One-pot stereospecific construction of cis-clerodane skeleton by means of doubly stereocontrolled cyclization: Total synthesis of linaridial
Abstract
Doubly stereocontrolled cyclization of the allylsilane derivative 1 followed by trapping of the enolate with ClCH2SMe gives in one-pot manner the decalone derivatve 5 in which all of the four contiguous diastereomeric centers of cis-clerodane skeleton have been secured. The total synthesis of linaridial 4 have been accomplished from...
Paper Details
Title
One-pot stereospecific construction of cis-clerodane skeleton by means of doubly stereocontrolled cyclization: Total synthesis of linaridial
Published Date
Jan 1, 1987
Journal
Volume
28
Issue
52
Pages
6645 - 6648
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