中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Hypervalent Iodine Reagents Enable Chemoselective Deboronative/Decarboxylative Alkenylation by Photoredox Catalysis

文献类型:期刊论文

作者Huang HC(黄汉初); Jia KF(贾坤方); Chen YY(陈以昀)
刊名Angew. Chem.-Int. Edit.
出版日期2015
卷号54期号:6页码:1881-1884
其他题名高价碘试剂通过可见光催化实现化学选择的脱硼脱羧烯基化反应
通讯作者陈以昀
英文摘要Chemoselective C(sp3) C(sp2) coupling reactions under mild reaction conditions are useful for synthesizing alkyl-substituted alkenes having sensitive functional groups. Reported here is a visible-light-induced chemoselective alkenylation through a deboronation/decarboxylation sequence under neutral aqueous reaction conditions at room temperature. This reaction represents the first hypervalent-iodineenabled radical decarboxylative alkenylation reaction, and a novel benziodoxole-vinyl carboxylic acid reaction intermediate was isolated. This C(sp3) C(sp2) coupling reaction leads to aryl-and acyl-substituted alkenes containing various sensitive functional groups. The excellent chemoselectivity, stable reactants, and neutral aqueous reaction conditions of the reaction suggest future biomolecule 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.201410176
语种英语
WOS记录号WOS:000349209200037
源URL[http://ir.sioc.ac.cn/handle/331003/39476]  
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
推荐引用方式
GB/T 7714
Huang HC,Jia KF,Chen YY. Hypervalent Iodine Reagents Enable Chemoselective Deboronative/Decarboxylative Alkenylation by Photoredox Catalysis[J]. Angew. Chem.-Int. Edit.,2015,54(6):1881-1884.
APA 黄汉初,贾坤方,&陈以昀.(2015).Hypervalent Iodine Reagents Enable Chemoselective Deboronative/Decarboxylative Alkenylation by Photoredox Catalysis.Angew. Chem.-Int. Edit.,54(6),1881-1884.
MLA 黄汉初,et al."Hypervalent Iodine Reagents Enable Chemoselective Deboronative/Decarboxylative Alkenylation by Photoredox Catalysis".Angew. Chem.-Int. Edit. 54.6(2015):1881-1884.

入库方式: OAI收割

来源:上海有机化学研究所

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