中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
The reaction of organozinc reagents with triftuoroacylated phosphonates: Synthesis of trifluoromethytated alpha, beta-unsaturated esters with an active methylene moiety

文献类型:期刊论文

作者Shen YC(沈延昌) ; Ni JH(倪家宏)
刊名Heteroatom Chem.
出版日期2004
卷号15期号:4页码:289-292
ISSN号1042-7163
其他题名有机锌化合物和三氟酰基膦酸的反应。合成具有活泼亚甲基的三氟甲基α,β-不饱和酸酯
通讯作者沈延昌
英文摘要The consecutive reaction of phosphonates 1 with n-butyllithium, trifluoroacetic anhydride, and organozinc compounds gives trifluoromethylated alpha, beta-unsaturated esters with an active methylene moiety and predominant Z-selectivity in 54-78% (3 steps) yields. (C) 2004 Wiley Periodicals, Inc.
学科主题氟化学
收录类别SCI
原文出处http://dx.doi.org/10.1002/hc.20018
语种英语
WOS记录号WOS:000221692900001
公开日期2013-02-21
源URL[http://202.127.28.38/handle/331003/17013]  
专题上海有机化学研究所_中科院有机氟化学重点实验室
推荐引用方式
GB/T 7714
Shen YC,Ni JH. The reaction of organozinc reagents with triftuoroacylated phosphonates: Synthesis of trifluoromethytated alpha, beta-unsaturated esters with an active methylene moiety[J]. Heteroatom Chem.,2004,15(4):289-292.
APA 沈延昌,&倪家宏.(2004).The reaction of organozinc reagents with triftuoroacylated phosphonates: Synthesis of trifluoromethytated alpha, beta-unsaturated esters with an active methylene moiety.Heteroatom Chem.,15(4),289-292.
MLA 沈延昌,et al."The reaction of organozinc reagents with triftuoroacylated phosphonates: Synthesis of trifluoromethytated alpha, beta-unsaturated esters with an active methylene moiety".Heteroatom Chem. 15.4(2004):289-292.

入库方式: OAI收割

来源:上海有机化学研究所

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