中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Au(III)-catalyzed ring opening reaction of 1-cyclopropyl-2-yn-1-ols with nucleophiles: highly efficient approach to (Z)-conjugated enynes

文献类型:期刊论文

作者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)
刊名New Journal of Chemistry
出版日期2007
卷号31页码:2041-2043
ISSN号1144-0546
通讯作者梁永民
中文摘要A 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.
学科主题材料科学与物理化学
收录类别SCI
资助信息the NSF (NSF-20621091;NSF-20672049)
语种英语
公开日期2013-11-01
源URL[http://210.77.64.217/handle/362003/4026]  
专题兰州化学物理研究所_固体润滑国家重点实验室
推荐引用方式
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.

入库方式: OAI收割

来源:兰州化学物理研究所

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