A new stereoselective approach for the synthesis of substituted 3-cyclopropylmethylene-1,3-dihydro-indol-2-one via the condensation reaction of cis-1-aryl-2-benzoyl-3,3-dicyanocyclopropanes with oxindole in water

被引：6
|
作者：
Zhou, Dong [1 ]
Yu, Haigang [1 ]
Liu, Ying [1 ]
Chen, Jie [1 ]
Deng, Hongmei [3 ]
Shao, Min [3 ]
Ren, Zhongjiao [1 ]
Cao, Weiguo [1 ,2 ]
机构：
[1] Shanghai Univ, Dept Chem, Shanghai 200444, Peoples R China
[2] Shanghai Inst Organ Chem, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China
[3] Shanghai Univ, Instrumental Anal & Res Ctr, Shanghai 200444, Peoples R China
来源：
TETRAHEDRON LETTERS | 2010年 / 51卷 / 41期
基金：
中国国家自然科学基金;
关键词：
Vinylcyclopropane; Cyclopropyl ketone; Water; Oxindole; Stereoselective synthesis; FRIEDEL-CRAFTS ALKYLATION; VINYL CYCLOPROPANES; ORGANIC-REACTIONS; ALPHA-KETOESTERS; VINYLCYCLOPROPANES; DERIVATIVES; PALLADIUM; KETONES; ROUTE;
D O I：
10.1016/j.tetlet.2010.08.025
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
A new stereoselective approach for the synthesis of substituted 3-cyclopropylmethylene-1,3-dihydroindol-2-one via the condensation reaction of cis-1-aryl-2-benzoyl-3,3-dicyanocyclopropanes with oxindole in water was achieved. (C) 2010 Elsevier Ltd. All rights reserved.
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页码：5473 / 5475
页数：3
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