Zhang Wen, Werness Jenny B, Tang Weiping
The School of Pharmacy and Department of Chemistry, University of Wisconsin, 777 Highland Avenue, Madison, Wisconsin 53705-2222, USA.
Org Lett. 2008 May 15;10(10):2023-6. doi: 10.1021/ol800334m. Epub 2008 Apr 25.
A de novo intramolecular hydroamination of conjugated enynes was developed using commercially available n-BuLi as a precatalyst. This hydroamination reaction successfully afforded allenyl-substituted pyrrolidines with up to 95% yield. One of the resulting allenyl pyrrolidines was converted to the natural products irniine and irnidine in three steps.
利用市售的正丁基锂作为预催化剂,开发了一种共轭烯炔的分子内直接氢胺化反应。该氢胺化反应成功地以高达95%的产率得到了烯丙基取代的吡咯烷。其中一种所得的烯丙基吡咯烷经三步反应转化为天然产物irniine和irnidine。