Chiral Guanidine-catalyzed 1,4-Addition Reaction of 5H-Oxazol-4-ones to Alkynones
Author:
Affiliation:
1. Graduate School of Material Science, University of Hyogo
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
http://www.journal.csj.jp/doi/pdf/10.1246/cl.2012.1675
Reference27 articles.
1. Organocatalytic Enantioselective Conjugate Addition to Alkynones
2. New, Chiral Phase Transfer Catalysts for Effecting Asymmetric Conjugate Additions of α-Alkyl-α-cyanoacetates to Acetylenic Esters
3. Asymmetric conjugate additions of α-substituted-α-cyanoacetates to acetylenic ketones by chiral phase transfer catalysis
4. A Stable Homodinuclear Biscobalt(III)-Schiff Base Complex for Catalytic Asymmetric 1,4-Addition Reactions of β-Keto Esters to Alkynones
5. Phase-Transfer Catalyzed Asymmetric Conjugate Additions of β-Ketoesters to Acetylenic Ketones
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1. Review on Asymmetric Catalysis Employing 5 H‐ Oxazol‐4‐Ones as α‐Hydroxy Carboxylic Acid Surrogates;Advanced Synthesis & Catalysis;2021-06-26
2. Recent Advances in Chiral Guanidine‐Catalyzed Enantioselective Reactions;Chemistry – An Asian Journal;2019-10-17
3. Conjugated enynones: preparation, properties and applications in organic synthesis;Russian Chemical Reviews;2019-03-01
4. Bifunctional iminophosphorane superbases: Potent organocatalysts for enantio- and diastereoselective Michael addition reactions;Tetrahedron;2018-09
5. Highly enantioselective allylic alkylation of 5 H -oxazol-4-ones with Morita-Baylis-Hillman carbonates;Tetrahedron;2018-08
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