Catalytic Asymmetric Synthesis of Spirooxindoles via Addition of Isothiocyanato Oxindoles to Aldehydes Under Dinuclear Nickel Schiff Base Catalysis

被引：51
作者：
Kato, Shota [1 ]
Kanai, Motomu [1 ]
Matsunaga, Shigeki [1 ,2 ]
机构：
[1] Univ Tokyo, Grad Sch Pharmaceut Sci, Bunkyo Ku, Tokyo 1130033, Japan
[2] Japan Sci & Technol Agcy, ACT C, Bunkyo Ku, Tokyo 1130033, Japan
来源：
CHEMISTRY-AN ASIAN JOURNAL | 2013年 / 8卷 / 08期
关键词：
asymmetric catalysis; asymmetric synthesis; oxindole; salen; spiro compounds; PICTET-SPENGLER REACTIONS; MANNICH-TYPE REACTIONS; ENANTIOSELECTIVE SYNTHESIS; SPIROCYCLIC OXINDOLES; HIGHLY EFFICIENT; 3,3'-PYRROLIDONYL SPIROOXINDOLES; MICHAEL/CYCLIZATION REACTION; MULTIPLE STEREOCENTERS; QUATERNARY CENTERS; NATURAL-PRODUCTS;
D O I：
10.1002/asia.201300251
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
引用
收藏
页码：1768 / 1771
页数：4
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