Gold(III) Chloride Catalyzed Synthesis of 1-Cyanoisoindoles
摘要:
A two-step synthesis of 1-cyanoisoindoles starting from ethynylbenzaldehyde is presented. The key step is a mild, high-yielding, gold-catalyzed rearrangement of N-allylic aminonitriles.
Gold(III) Chloride Catalyzed Synthesis of 1-Cyanoisoindoles
作者:Thomas S. A. Heugebaert、Christian V. Stevens
DOI:10.1021/ol902031f
日期:2009.11.5
A two-step synthesis of 1-cyanoisoindoles starting from ethynylbenzaldehyde is presented. The key step is a mild, high-yielding, gold-catalyzed rearrangement of N-allylic aminonitriles.