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Direct Construction of NOBINs via Domino Arylation and Sigmatropic Rearrangement Reactions 被引量:3

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摘要 of main observation and conclusion Privileged 2-amino-2,-hydroxy-l/l,-binaphthyl(NOBIN)frameworks were constructed through a novel domino arylation of naphthylhydroxylamines with diarylhalonium salts and sigmatropic rearrangement in a transition metal-free fashion.This protocol bears broad substrate generality and proceeds under mild reaction conditions,affording diversified NOBINs in high efficiency with absolute regiocontrol during the rearrangement process.Optically active product was accessible by chiral A/-heterocyclic carbene-catalyzed kinetic resolution in one pot or diastereoselective[3,3]-rearrangement guided by a removable chiral auxiliary.Remarkably,diarylchloronium and diarylbrominium salts have been employed as arylation reagents for the first time in assembling such representative biaryl frameworks.
出处 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2020年第12期1503-1514,共12页 中国化学(英文版)
基金 We are grateful for financial support from the National Natural Science Foundation of China(Nos.21772081,21825105,21801117) Guangdong Provincial Key Laboratory of Catalysis(No.2020B121201002) the Guangdong Innovative Program(No.2019BT02Y335) the Shenzhen Special Funds(No.JCYJ2018030-5123508258) Shenzhen Nobel Prize Scientists LaboratoryProject(No.C17213101).
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