摘要
A simple and biomimetic synthetic strategy for indolo[3,2-a]carbazoles has been developed. Our approach involved the efficient conversion of 2-(3'-indolyl)tryptophan derivatives into the corresponding cc-keto esters and the subsequent aromatic cyclisation of these intermediates to construct the characteristic heteroaryl-condensed carbazole core.
- 出版日期2015-1-8
- 单位贵州省中国科学院天然产物化学重点实验室; 贵州大学