Visible light photocatalytic acyldifluoroalkylation of unactivated alkenes for the direct synthesis of gem- difluorinated ketones

Visible light photocatalytic acyldifluoroalkylation of unactivated alkenes for the direct synthesis of gem- difluorinated ketones
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未活化烯烃的可见光催化酰基二氟烷基化直接合成偕二氟酮

DOI:
10.1039/c9qo00136k
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发表时间:
2019
影响因子:
5.4
通讯作者:
Zhu Gangguo
Zhu Gangguo
中科院分区:
化学1区
文献类型:
--
作者:
Zhou Yulu;Xiong Zhimin;Qiu Jiayan;Kong Lichun;Zhu Gangguo

文献摘要

被引文献

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以二氟乙酸为二氟烷基化试剂,邻苯二甲酸二丁酯为氧化剂,在可见光下进行了未活化烯烃的酰基二氟烷基化反应。本发明在室温下有效地合成了多种偕二氟代环酮,包括色满-4-酮、茚满酮、3,4-二氢萘-1(2 H)-酮、2,3-二氢喹啉-4(1H)-酮和环戊二烯-2-烯酮,具有优异的官能团相容性。
A visible-light-induced acyldifluoroalkylation of unactivated alkenes with difluoroacetic acids as the difluoroalkylation reagent and PhI(OAc)2 as the oxidant is described. Various gem-difluorinated cyclic ketones, including chroman-4-ones, indanones, 3,4-dihydronaphthalen-1(2H)-ones, 2,3-dihydroquinolin-4(1H)-ones, and cyclopent-2-enones, are efficiently synthesized with excellent functional group compatibility at room temperature.