作者:Tomoaki Nakamura、Shin-ichi Shirokawa、Seijiro Hosokawa、Atsuo Nakazaki、Susumu Kobayashi
DOI:10.1021/ol052871p
日期:2006.2.1
[reaction: see text] The first enantioselective total synthesis of convolutamydines B and E has been achieved using our vinylogous Mukaiyama aldol reaction. The synthesis features highly diastereoselective vinylogous Mukaiyama aldol reaction with isatin instead of aldehydes to construct a chiral center of convolutamydines. Additionally, the absolute configuration of natural convolutamydine B has been
[反应:见正文]使用我们的乙烯基Mukaiyama醛醇缩合反应已实现了卷积嘧啶B和E的首次对映选择性全合成。该合成具有高度非对映选择性的乙烯基Mukaiyama aldol反应,该反应与靛红代替醛,构成了卷积糊精的手性中心。另外,已经通过其CD光谱将天然卷积亚胺B的绝对构型确定为R。