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Au(III)-catalyzed ring opening reaction of 1-cyclopropyl-2-yn-1-ols with nucleophiles: highly efficient approach to (Z)-conjugated enynes
Department固体润滑国家重点实验室
Xiao HQ(肖慧泉); Shu XZ(舒兴中); Ji KG(纪克攻); Qi CZ(齐晨泽); Liang YM(梁永民)
2007
Source PublicationNew Journal of Chemistry
ISSN1144-0546
Volume31Pages:2041-2043
AbstractA highly efficient approach to (Z)-conjugated enynes has been developed by utilizing an Au(III)-catalyzed ring opening reaction of 1-cyclopropyl-2-yn-1-ols with nucleophiles under mild conditions; the method is valuable due to the excellent yield and high regio- and stereoselectivity.
Subject Area材料科学与物理化学
Funding Organizationthe NSF (NSF-20621091;NSF-20672049)
Indexed BySCI
Language英语
Document Type期刊论文
Identifierhttp://ir.licp.cn/handle/362003/4026
Collection固体润滑国家重点实验室(LSL)
Corresponding AuthorLiang YM(梁永民)
Recommended Citation
GB/T 7714
Xiao HQ,Shu XZ,Ji KG,et al. Au(III)-catalyzed ring opening reaction of 1-cyclopropyl-2-yn-1-ols with nucleophiles: highly efficient approach to (Z)-conjugated enynes[J]. New Journal of Chemistry,2007,31:2041-2043.
APA 肖慧泉,舒兴中,纪克攻,齐晨泽,&梁永民.(2007).Au(III)-catalyzed ring opening reaction of 1-cyclopropyl-2-yn-1-ols with nucleophiles: highly efficient approach to (Z)-conjugated enynes.New Journal of Chemistry,31,2041-2043.
MLA 肖慧泉,et al."Au(III)-catalyzed ring opening reaction of 1-cyclopropyl-2-yn-1-ols with nucleophiles: highly efficient approach to (Z)-conjugated enynes".New Journal of Chemistry 31(2007):2041-2043.
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