Meichen Xu , Pandaram Sakthivel , Zongyang Ma , Juntao Ye
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Alkylcyanation of unactivated alkenes via photoinduced hydrogen atom transfer and 1,4-cyano migration
1,2-Dicarbofunctionalization of alkenes represents a step-economical strategy for introducing two functional groups simultaneously in organic synthesis. Herein, we report a visible-light-driven alkylcyanation of unactivated alkenes via hydrogen atom transfer (HAT) and cyano migration. Mechanistic studies suggest that a quinuclidineboryl radical serves as an effective hydridic HAT catalyst, facilitating the generation of electrophilic alkyl radicals. This method features mild reaction conditions and good compatibility with a diverse array of functional groups.
期刊介绍:
Tetrahedron Letters provides maximum dissemination of outstanding developments in organic chemistry. The journal is published weekly and covers developments in techniques, structures, methods and conclusions in experimental and theoretical organic chemistry. Rapid publication of timely and significant research results enables researchers from all over the world to transmit quickly their new contributions to large, international audiences.