Enantioselective synthesis of chiral sulfones by Ir-catalyzed asymmetric hydrogenation: a facile approach to the preparation of chiral allylic and homoallylic compounds.

Enantioselective synthesis of chiral sulfones by Ir-catalyzed asymmetric hydrogenation: a facile approach to the preparation of chiral allylic and homoallylic compounds.
复制标题

DOI:
10.1021/ja306731u
复制
发表时间:
2012-08
影响因子:
15
通讯作者:
Taigang Zhou;B. Peters;M. F. Maldonado;T. Govender;P. Andersson
Taigang Zhou;B. Peters;M. F. Maldonado;T. Govender;P. Andersson
中科院分区:
化学1区
文献类型:
--
作者:
Taigang Zhou;B. Peters;M. F. Maldonado;T. Govender;P. Andersson

文献摘要

被引文献

相似文献

发展了一种高效的不饱和砜的不对称选择性铱催化加氢反应。手性环状和非环状砜的产生在良好的对映选择性(高达98%ee)。与Ramberg-Bäcklund重排反应相结合,该反应提供了一种新的路线,手性烯丙基和高烯丙基化合物具有优异的对映选择性(高达97%ee)和高产率(高达94%)。
A highly efficient and enantioselective Ir-catalyzed hydrogenation of unsaturated sulfones was developed. Chiral cyclic and acyclic sulfones were produced in excellent enantioselectivities (up to 98% ee). Coupled with the Ramberg-Bäcklund rearrangement, this reaction offers a novel route to chiral allylic and homoallylic compounds in excellent enantioselectivities (up to 97% ee) and high yields (up to 94%).