The first enantioselective total synthesis of (-)-arisugacin A

The first enantioselective total synthesis of (-)-arisugacin A
复制标题

DOI:
10.1016/s0040-4039(02)02094-4
复制
发表时间:
2002-11-25
影响因子:
1.8
通讯作者:
Hsung, RP
Hsung, RP
中科院分区:
化学4区
文献类型:
--
作者:
Cole, KP;Hsung, RP

文献摘要

被引文献

相似文献

本文首次用17步对映选择性合成了(-)-亚柳糖酸A,采用CBS不对称酮还原和高度立体选择性的形式[3+3]环加成方法。这种对映体的简明合成明确地证实了绝对构型的原始分配。(C) 2002 Elsevier Science Ltd.版权所有。
The first enantioselective synthesis of (-)-arisugacin A in 17 steps is described here, featuring a CBS asymmetric ketone reduction and a highly stereoselective formal [3+3] cycloaddition approach. This concise synthesis of the enantiomer unambiguously confirms the original assignment of the absolute configuration. (C) 2002 Elsevier Science Ltd. All rights reserved.