Tetrahedron

Gold (I)-catalyzed rearrangement of alkynylaziridine indoles for the synthesis of spiro-tetrahydro-β-carbolines

YF Yang, LH Li, YT He, JY Luo, YM Liang

文献索引：Yang, Yan-Fang; Li, Lian-Hua; He, Yu-Tao; Luo, Jian-Yi; Liang, Yong-Min Tetrahedron, 2014 , vol. 70, # 3 p. 702 - 707

全文：HTML全文

被引用次数: 4

摘要

Abstract Functionalized spiro-tetrahydro-β-carbolines were formed by an efficient gold (I)- catalyzed rearrangement reaction of alkynylaziridine indoles. The reaction involved a Friedel–Crafts type intramolecular reaction of alkynylaziridine indoles, following by hydroamination of aminoallene intermediate.