Enantioselective Asymmetric Michael Addition of Cyclic Diketones to β,γ-Unsaturated α-Keto Esters
出版年份 2012 全文链接
标题
Enantioselective Asymmetric Michael Addition of Cyclic Diketones to β,γ-Unsaturated α-Keto Esters
作者
关键词
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出版物
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
Volume 2012, Issue 19, Pages 3691-3696
出版商
Wiley
发表日期
2012-05-23
DOI
10.1002/ejoc.201200179
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- (2011) José Alemán et al. CHEMISTRY-A EUROPEAN JOURNAL
- Organocatalytic Michael Addition of Naphthoquinone with α,β-Unsaturated Ketones: Primary Amine Catalyzed Asymmetric Synthesis of Lapachol Analogues
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- Highly Enantioselective Organocatalytic Michael Addition of 2-Hydroxy- 1,4-naphthoquinone to β,γ-Unsaturated α-Oxo Esters
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- (2009) Tor E. Kristensen et al. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
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- Catalytic, Asymmetric Michael Reactions of Cyclic Diketones with β,γ-Unsaturated α-Ketoesters
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- (2008) Magnus Rueping et al. ADVANCED SYNTHESIS & CATALYSIS
- Asymmetric Organocatalysis: An Efficient Enantioselective Access to Benzopyranes and Chromenes
- (2008) Magnus Rueping et al. CHEMISTRY-A EUROPEAN JOURNAL
- Chiral Squaramide Derivatives are Excellent Hydrogen Bond Donor Catalysts
- (2008) Jeremiah P. Malerich et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
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