Zuo Zhijun, Yang Xin, Liu Jingjing, Nan Jiang, Bai Lu, Wang Yaoyu, Luan Xinjun
J Org Chem. 2015 Mar 20;80(6):3349-56. doi: 10.1021/acs.joc.5b00316. Epub 2015 Mar 5.
An intermolecular spiroannulation reaction of appropriately substituted 2-arylphenols with internal alkynes has been developed by using a Ru(II) catalyst and an oxidant. This transformation was realized by a phenol-directed C-H activation, migratory insertion of the alkyne, and subsequent dearomatization of the phenolic ring, providing a broad range of highly functionalized spirocyclic compounds in moderate yields with high regioselectivity.
通过使用钌(II)催化剂和氧化剂,已开发出一种适当取代的2-芳基苯酚与内炔的分子间螺环化反应。这种转化是通过苯酚导向的C-H活化、炔烃的迁移插入以及随后酚环的去芳构化实现的,以中等产率和高区域选择性提供了多种高度官能化的螺环化合物。