Copper-catalyzed decarboxylative cross-coupling of cinnamic acids and ACCN via single electron transfer

doi:10.1039/c5ob02677f

	Copper-catalyzed decarboxylative cross-coupling of cinnamic acids and ACCN via single electron transfer
Department	OSSO国家重点实验室
	Gao B(高宝)1,2; Xie YJ(谢银君)1; Yang L(杨磊)1 ; Huang HM(黄汉民)1 ; Huang HM(黄汉民)
	2016
Source Publication	Organic & Biomolecular Chemistry
ISSN	1477-0520
Volume	14 Issue:8 Pages:2399-2402
Abstract	A novel and convenient method for the synthesis of β,γ-unsaturated nitriles using ACCN (1,1′-azobis(cyclohexane-1-carbonitrile)) as a cyano source was described. This reaction was amenable to a broad range of substrates and provided the desired β,γ-unsaturated nitriles containing an all-carbon quaternary carbon center in moderate yields with high selectivity via single electron transfer and decarboxylation.
Subject Area	物理化学与绿色催化
DOI	10.1039/c5ob02677f
Funding Organization	the Chinese Academy of Sciences;the National Natural Science Foundation of China (21222203;21372231;21133011)
Indexed By	SCI
If	3.564
Language	英语
Funding Project	有机功能材料研究组
compositor	第一作者单位
Citation statistics	Cited Times:27[WOS] [WOS Record] [Related Records in WOS]
Document Type	期刊论文
Identifier	http://ir.licp.cn/handle/362003/19755
Collection	羰基合成与选择氧化国家重点实验室（OSSO）
Corresponding Author	Huang HM(黄汉民)
Affiliation	1.Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Peoples R China 2.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
Recommended Citation GB/T 7714	Gao B,Xie YJ,Yang L,et al. Copper-catalyzed decarboxylative cross-coupling of cinnamic acids and ACCN via single electron transfer[J]. Organic & Biomolecular Chemistry,2016,14(8):2399-2402.
APA	Gao B,Xie YJ,Yang L,Huang HM,&黄汉民.(2016).Copper-catalyzed decarboxylative cross-coupling of cinnamic acids and ACCN via single electron transfer.Organic & Biomolecular Chemistry,14(8),2399-2402.
MLA	Gao B,et al."Copper-catalyzed decarboxylative cross-coupling of cinnamic acids and ACCN via single electron transfer".Organic & Biomolecular Chemistry 14.8(2016):2399-2402.

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