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Catalytic C2 prenylation of unprotected indoles:Late‐stage diversification of peptides and two‐step total synthesis of tryprostatin B
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作者 Yan‐cheng Hu Ying Li +4 位作者 Ding‐Wei Ji Heng Liu Hao Zheng Gong Zhang qing‐an chen 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 2021年第9期1593-1607,共15页
C2 prenylated indoles are widespread in a variety of bioactive natural alkaloids.Therefore,theselective installation of prenyl group at C2 position of NH indoles is of great significance.However,the known protocols ge... C2 prenylated indoles are widespread in a variety of bioactive natural alkaloids.Therefore,theselective installation of prenyl group at C2 position of NH indoles is of great significance.However,the known protocols generally require a multi‐step procedure and stoichiometric promoters.Hereinwe develop a one‐step C2 prenylation of NH indole with cheap tert‐prenyl alcohol enabled by acidcatalysis.Salient features include good regioselectivity,step‐and atom‐economy,broad substratescope,and simple catalytic system.The mechanistic investigations demonstrate that both C2prenylation and C3 prenylation/migration pathways are engaged in the reaction.Notably,this practicalstrategy can be applied to the late‐stage diversification of tryptophan‐based peptides and concisesynthesis of tryprostatin B. 展开更多
关键词 Indole prenylation Step economy Atom economy TRYPTOPHAN Peptide diversification Total synthesis
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