Palladium catalyzed coupling of organostannanes with vinyl epoxides
作者:David R. Tueting、Antonio M. Echavarren、J.K. Stille
DOI:10.1016/0040-4020(89)80010-9
日期:1989.1
The coupling reaction of organotin reagents with vinyl epoxides, catalyzed by palladium, takes place at ambient temperatures, regioselectively, giving predominately the 1,4-addition product. Both aryl- and vinylstannanes undergo coupling in high yields, while acetylenic, allylic and benzylic tin reagents either give low yields or fail to couple. Although the double bond geometry in the vinylstannane