中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Highly Regioselective Synthesis of 2,3,5-Trisubstituted Furans via Phosphine-Catalyzed Ring-Opening Cycloisomerization Reactions of Cyclopropenyl Dicarboxylates

文献类型:期刊论文

作者Chen J(陈洁) ; Ni SJ(倪圣君) ; Ma SM(麻生明)
刊名Synlett
出版日期2011
期号7页码:931-934
ISSN号0936-5214
其他题名通过膦催化的环丙烯基二羧酸酯的开环异构化反应, 高区域选择性合成2,3,5-三取代呋喃类化合物
通讯作者麻生明
英文摘要Different 2,3,5-trisubstituted furans have been regioselectively synthesized through a ring-opening cycloisomerization of functionalized cyclopropenyl carboxylates with moderate to excellent yields by using tri(2-furanyl)phosphine as the catalyst.
学科主题有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1055/s-0030-1259904
语种英语
WOS记录号WOS:000289411900014
公开日期2013-01-16
源URL[http://202.127.28.38/handle/331003/12240]  
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
Chen J,Ni SJ,Ma SM. Highly Regioselective Synthesis of 2,3,5-Trisubstituted Furans via Phosphine-Catalyzed Ring-Opening Cycloisomerization Reactions of Cyclopropenyl Dicarboxylates[J]. Synlett,2011(7):931-934.
APA 陈洁,倪圣君,&麻生明.(2011).Highly Regioselective Synthesis of 2,3,5-Trisubstituted Furans via Phosphine-Catalyzed Ring-Opening Cycloisomerization Reactions of Cyclopropenyl Dicarboxylates.Synlett(7),931-934.
MLA 陈洁,et al."Highly Regioselective Synthesis of 2,3,5-Trisubstituted Furans via Phosphine-Catalyzed Ring-Opening Cycloisomerization Reactions of Cyclopropenyl Dicarboxylates".Synlett .7(2011):931-934.

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。