We report on N,N-bidentate-chelation-assistedα-and β-olefinic C–H alkenylation of aryl alkenes in ethanol to afford aryl dienes/trienes with excellent regio-and stereo-selectivities.The reaction of 2-alkenyl benzyl...We report on N,N-bidentate-chelation-assistedα-and β-olefinic C–H alkenylation of aryl alkenes in ethanol to afford aryl dienes/trienes with excellent regio-and stereo-selectivities.The reaction of 2-alkenyl benzylamine and benzoic acid derived substrates proceeded through six-membered exo-cyclo-metallation and seven-membered endo-cyclometallation.The aerobic protocols feature wide functional-ity tolerance,high selectivities and yields,mild conditions and scalable preparation,and the directing group can be easily removed to afford Boc-protected amine by simple reduction.展开更多
基金We gratefully acknowledge the National Natural Science Foundation of China(NSFC)(21672048 and 81570989)Natural Science Foundation of Zhejiang Province(ZJNSF)(LY19B020006)+1 种基金Major Project of Hangzhou Health Science and Technology Plan(Z20200046)Key Subject of Stomatology in Hangzhou for financial support.
文摘We report on N,N-bidentate-chelation-assistedα-and β-olefinic C–H alkenylation of aryl alkenes in ethanol to afford aryl dienes/trienes with excellent regio-and stereo-selectivities.The reaction of 2-alkenyl benzylamine and benzoic acid derived substrates proceeded through six-membered exo-cyclo-metallation and seven-membered endo-cyclometallation.The aerobic protocols feature wide functional-ity tolerance,high selectivities and yields,mild conditions and scalable preparation,and the directing group can be easily removed to afford Boc-protected amine by simple reduction.
