Organocatalytic Domino Double Michael Reaction of Ethyl (E)-7-Oxohept-2-enoate and α,β-Unsaturated Aldehydes: Efficient Asymmetric Synthesis of Cyclohexanes with Four Contiguous Stereocenters
Author:
Publisher
Georg Thieme Verlag KG
Subject
Organic Chemistry,Catalysis
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0030-1260469.pdf
Cited by 21 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
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3. Construction of Seven Contiguous Chiral Centers by Two Methods: Quadruple Michael Addition vs Stepwise Double-Double Michael Addition Controlled by Adding Speed of Michael Acceptor;ChemistrySelect;2016-07-01
4. Substrate-Controlled Synthesis of Functionalized Cyclohexanes with Four Stereocenters by Organocatalytic Asymmetric Domino Reactions Between γ-Nitro Ketone and Enone;European Journal of Organic Chemistry;2015-12-02
5. Regioselectivity switch in chiral amine-catalysed asymmetric addition of aldehydes to reactive enals;Chemical Communications;2015
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