Zinc(II)-Catalyzed Intermolecular Hydrative Aldol Reactions of 2-En-1-ynamides with Aldehydes and Water to form Branched Aldol Products Regio- and Stereoselectively
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Title
Zinc(II)-Catalyzed Intermolecular Hydrative Aldol Reactions of 2-En-1-ynamides with Aldehydes and Water to form Branched Aldol Products Regio- and Stereoselectively
Authors
Keywords
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Journal
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 54, Issue 12, Pages 3812-3816
Publisher
Wiley
Online
2015-01-21
DOI
10.1002/anie.201411689
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- (2013) Jeremy Kister et al. ORGANIC LETTERS
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- (2013) Zheng-Wang Chen et al. TETRAHEDRON
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- (2012) Xiubin Li et al. ADVANCED SYNTHESIS & CATALYSIS
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- (2012) William E. Brenzovich ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
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- (2012) Tadashi Tachinami et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
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- (2012) Yuki Mukaeda et al. ORGANIC LETTERS
- Enantioselective Iridium-Catalyzed Vinylogous Reformatsky-Aldol Reaction from the Alcohol Oxidation Level: Linear Regioselectivity by Way of Carbon-Bound Enolates
- (2011) Abbas Hassan et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Mild chemo-selective hydration of terminal alkynes catalysed by AgSbF6
- (2011) Mathieu Bui The Thuong et al. CHEMICAL COMMUNICATIONS
- The Vinylogous Aldol and Related Addition Reactions: Ten Years of Progress†
- (2011) Giovanni Casiraghi et al. CHEMICAL REVIEWS
- Asymmetric Vinylogous Mukaiyama Aldol Reaction of Aldehyde-Derived Dienolates
- (2011) Marc T. Gieseler et al. ORGANIC LETTERS
- Gold-Catalyzed Synthesis of α-Fluoro Acetals and α-Fluoro Ketones from Alkynes
- (2010) Teresa de Haro et al. ADVANCED SYNTHESIS & CATALYSIS
- Fluorine-Enabled Cationic Gold Catalysis: Functionalized Hydration of Alkynes
- (2010) Weibo Wang et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
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- (2010) Gwilherm Evano et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Ynamides: A Modern Functional Group for the New Millennium
- (2010) Kyle A. DeKorver et al. CHEMICAL REVIEWS
- Highly Diastereoselective Preparation of Homoallylic Alcohols Containing Two Contiguous Quaternary Stereocenters in Acyclic Systems from Simple Terminal Alkynes
- (2010) Bishnu Dutta et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Development of the First Iron Chloride-Catalyzed Hydration of Terminal Alkynes
- (2009) Xiao-Feng Wu et al. ADVANCED SYNTHESIS & CATALYSIS
- A unique approach to aldol products for the creation of all-carbon quaternary stereocentres
- (2009) Jaya Prakash Das et al. Nature Chemistry
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- (2008) Hironobu Kanemitsu et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- [(NHC)AuI]-Catalyzed Acid-Free Alkyne Hydration at Part-per-Million Catalyst Loadings
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