Facile Creation of 3-Indolyl-3-hydroxy-2-oxindoles by an Organocatalytic Enantioselective Friedel-Crafts Reaction of Indoles with Isatins
出版年份 2010 全文链接
标题
Facile Creation of 3-Indolyl-3-hydroxy-2-oxindoles by an Organocatalytic Enantioselective Friedel-Crafts Reaction of Indoles with Isatins
作者
关键词
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出版物
ADVANCED SYNTHESIS & CATALYSIS
Volume 352, Issue 5, Pages 833-838
出版商
Wiley
发表日期
2010-03-06
DOI
10.1002/adsc.200900851
参考文献
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- (2009) Junji Itoh et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
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- (2009) Marco Bandini et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
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- (2009) Fei Xue et al. Chemistry-An Asian Journal
- Asymmetric Aldol Reaction of Acetaldehyde and Isatin Derivatives for the Total Syntheses ofent-Convolutamydine E and CPC-1 and a Half Fragment of Madindoline A and B
- (2009) Takahiko Itoh et al. ORGANIC LETTERS
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- (2008) Qiang Kang et al. CHEMISTRY-A EUROPEAN JOURNAL
- Supramolecular Synthesis of 3-Indolyl-3-hydroxy Oxindoles under Neutral Conditions in Water
- (2008) V. Pavan Kumar et al. JOURNAL OF ORGANIC CHEMISTRY
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- (2008) Tohru Ueda et al. ORGANIC LETTERS
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- (2008) Lirong Song et al. ORGANIC LETTERS
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- (2007) Martin J. Wanner et al. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
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