中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
An efficient synthesis of 4-halo-5-hydroxyfuran-2(5H)-ones via the sequential halolactonization and gamma-hydroxylation of 4-aryl-2,3-alkadienoic acids

文献类型:期刊论文

作者Ma SM(麻生明) ; Wu B(吴滨) ; Shi ZJ(施章杰)
刊名J. Org. Chem.
出版日期2004
卷号69期号:4页码:1429-1431
ISSN号0022-3263
其他题名4-芳基-2,3-联烯酸的卤代环化及-羟基化合成4-卤代-5-羟基-2(5H)-呋喃酮
通讯作者麻生明
英文摘要4-Halo-5-hydroxyfuran-2(5H)-ones were synthesized via the efficient sequential halolactonization-hydroxylation reaction of 4-aryl-2,3-allenoic acids with 12 or CuX2 (X = Br or Cl) in moderate to good yields. The structures of the products were established by the X-ray single-crystal diffraction study of 3-methyl-4-iodo-5-phenyl-5-hydroxyl-2(5H)-furanone (2a). A rationale for this reaction was discussed based on some brief mechanistic study.
学科主题有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1021/jo0355698
语种英语
WOS记录号WOS:000188955400066
公开日期2013-01-15
源URL[http://202.127.28.38/handle/331003/11984]  
专题上海有机化学研究所_金属有机化学国家重点实验室
推荐引用方式
GB/T 7714
Ma SM,Wu B,Shi ZJ. An efficient synthesis of 4-halo-5-hydroxyfuran-2(5H)-ones via the sequential halolactonization and gamma-hydroxylation of 4-aryl-2,3-alkadienoic acids[J]. J. Org. Chem.,2004,69(4):1429-1431.
APA 麻生明,吴滨,&施章杰.(2004).An efficient synthesis of 4-halo-5-hydroxyfuran-2(5H)-ones via the sequential halolactonization and gamma-hydroxylation of 4-aryl-2,3-alkadienoic acids.J. Org. Chem.,69(4),1429-1431.
MLA 麻生明,et al."An efficient synthesis of 4-halo-5-hydroxyfuran-2(5H)-ones via the sequential halolactonization and gamma-hydroxylation of 4-aryl-2,3-alkadienoic acids".J. Org. Chem. 69.4(2004):1429-1431.

入库方式: OAI收割

来源:上海有机化学研究所

浏览0
下载0
收藏0
其他版本

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。