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作 者:Zhihong Zhu Weilu Zhang Yizhi Zhang Shanshan Liu Xiao Shen
出 处:《CCS Chemistry》2023年第2期325-333,共9页中国化学会会刊(英文)
基 金:the National Natural Science Foundation of China(grant no.21901191);the Fundamental Research Funds for the Central Universities,and Wuhan University for financial support.
摘 要:Herein we report the first[4+1]cyclization-aromatization reaction of acylsilanes andα,β-unsaturated ketones.The unprecedented visible-light-induced reaction proceeded through mild conditions without addition of any catalyst or additive,affording a variety of furans with broad substrate scope and good functional-group tolerance.The synthetic utility of the method was demonstrated by various downstream transformations of the otherwise difficult-to-access sulfone-containing silyl furans.The mechanism study reveals that 1,4-diketones are not likely to be the intermediates of the reaction.
关 键 词:acylsilane α β-unsaturated ketone CARBENE photo chemistry cyclization-aromatization FURAN
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