Stereoselective synthesis of the C1–C20 segment of the microsclerodermins A and B
作者:S. Chandrasekhar、S. Shameem Sultana
DOI:10.1016/j.tetlet.2006.07.107
日期:2006.10
An enantioselective route for the synthesis of key fragment C1–C20 resident in microsclerodermins A and B is described. The route features deoxygenative rearrangement of an hydroxy-alkynoate and a highly enantio- and diastereo-controled iterative dihydroxylation as key reactions, starting from S-(−)-citronellol.
描述了对映体选择性路线,该路线用于合成驻留在微核蛋白A和B中的关键片段C1-C20。该路线以羟基链烷酸酯的脱氧重排以及高度对映体和非对映体控制的迭代二羟基化为关键反应,从S -(-)-香茅醇开始。