An Expedient Synthesis of Oxindole Dimers by Direct Oxidative Dimerization of Oxindoles

被引：16
作者：
Lee, Hyun Ju [1 ,2 ]
Lee, Sangku [3 ]
Lim, Jin Woo [1 ,2 ]
Kim, Jae Nyoung [1 ,2 ]
机构：
[1] Chonnam Natl Univ, Dept Chem, Kwangju 500757, South Korea
[2] Chonnam Natl Univ, Inst Basic Sci, Kwangju 500757, South Korea
[3] KRIBB, Immune Modulator Res Ctr, Taejon 305806, South Korea
来源：
BULLETIN OF THE KOREAN CHEMICAL SOCIETY | 2013年 / 34卷 / 08期
基金：
新加坡国家研究基金会;
关键词：
Oxindole dimers; Oxidative dimerization; Manganese(BI) acetate; Oxindoles; CATALYZED AEROBIC DEHYDROGENATION; ENANTIOSELECTIVE TOTAL-SYNTHESIS; C-H; DERIVATIVES; CYCLIZATION; CYCLOHEXANONES; STEREOCENTERS; CHIMONANTHINE; CALYCANTHINE; ARYLATION;
D O I：
10.5012/bkcs.2013.34.8.2446
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
Oxindole dimers have been used as intermediates in the synthesis of various cyclotryptamine alkaloids. An efficient direct synthesis of oxindole dimers has been carried out from 3-substituted oxindoles via an oxidative dimerization using manganese(BI) acetate or copper acetate/silver acetate system.
引用
收藏
页码：2446 / 2450
页数：5
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