New strategy for this construction of carbapenems. Total synthesis of 6-epi PS-5 and PS-5.
作者:Ari M.P. Koskinen、Mehran Ghiaci
DOI:10.1016/s0040-4039(00)94734-8
日期:1990.1
developed. The pyrrolidine ring is first constructed, appended with the required side chains, and the β-lactam ring is then annealed. We have demonstrated the utility of the approach to the asymmetric synthesis of antibiotics 6-epi PS-5 and PS-5.
已经开发出战略上新颖的
碳青霉
烯方法。首先构建
吡咯烷环,并附加所需的侧链,然后将β-内
酰胺环退火。我们已经证明了该方法在
抗生素6-epi
PS-5和
PS-5的不对称合成中的实用性。