Dual Hypervalent Iodine(III) Reagents and Photoredox Catalysis Enable Decarboxylative Ynonylation under Mild Conditions
Huang HC(黄汉初); Zhang GJ(张国晋); Chen YY(陈以昀)
刊名Angew. Chem.-Int. Edit.
2015
卷号54期号:27页码:7872-7876
其他题名高价碘促进的脱羧炔酮化反应在温和光催化条件下进行
通讯作者陈以昀
英文摘要A combination of hypervalent iodine(III) reagents (HIR) and photoredox catalysis with visible light has enabled chemoselective decarboxylative ynonylation to construct ynones, ynamides, and ynoates. This ynonylation occurs effectively under mild reaction conditions at room temperature and on substrates with various sensitive and reactive functional groups. The reaction represents the first HIR/photoredox dual catalysis to form acyl radicals from -ketoacids, followed by an unprecedented acyl radical addition to HIR-bound alkynes. Its efficient construction of an mGlu5 receptor inhibitor under neutral aqueous conditions suggests future visible-light-induced biological applications.
学科主题生命有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1002/anie.201502369
语种英语
WOS记录号WOS:000356886600024
内容类型期刊论文
源URL[http://ir.sioc.ac.cn/handle/331003/39510]  
专题上海有机化学研究所_生命有机化学国家重点实验室
作者单位中科院上海有机化学研究所, 生命有机化学国家重点实验室
推荐引用方式
GB/T 7714
Huang HC,Zhang GJ,Chen YY. Dual Hypervalent Iodine(III) Reagents and Photoredox Catalysis Enable Decarboxylative Ynonylation under Mild Conditions[J]. Angew. Chem.-Int. Edit.,2015,54(27):7872-7876.
APA 黄汉初,张国晋,&陈以昀.(2015).Dual Hypervalent Iodine(III) Reagents and Photoredox Catalysis Enable Decarboxylative Ynonylation under Mild Conditions.Angew. Chem.-Int. Edit.,54(27),7872-7876.
MLA 黄汉初,et al."Dual Hypervalent Iodine(III) Reagents and Photoredox Catalysis Enable Decarboxylative Ynonylation under Mild Conditions".Angew. Chem.-Int. Edit. 54.27(2015):7872-7876.
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