Stereoselective synthesis of macrolactin a analogues. Part 2: The C1–C14 fragment
作者:Thierry J. Benvegnu、RenéL. Grée
DOI:10.1016/0040-4020(96)00667-9
日期:1996.9
A synthetic approach to the C1–C14part of Macrolactin A analogues is presented. The sequence involving hydroboration-Pdo coupling reaction was found to be the most efficient in term of chemio- and stereo-selectivity to prepare the sensitive and functionalized E,Z diene unit.