The Asymmetric Vinylogous Mukaiyama Aldol Reaction
Author:
Affiliation:
1. Institute of Organic Chemistry; Gottfried Wilhelm Leibniz University of Hannover; Schneiderberg 1b 30167 Hannover Germany
Publisher
John Wiley & Sons, Inc.
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/0471264180.or098.02/fullpdf
Reference663 articles.
1. Recent Advances in Vinylogous Aldol Reactions and Their Applications in the Syntheses of Natural Products
2. Catalytic, Enantioselective, Vinylogous Aldol Reactions
3. Recent Advances in Asymmetric Aldol Reaction of Masked Acetoacetic Esters Promoted by Ti(IV) / BINOL: A New Methodology, Non-Linear Effects and Autoinduction
4. The Vinylogous Aldol Reaction: A Valuable, Yet Understated Carbon−Carbon Bond-Forming Maneuver
5. The Principle of Vinylogy.
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1. Oxazaborolidinone-Mediated Asymmetric Bisvinylogous Mukaiyama Aldol Reaction;Organic Letters;2021-11-05
2. Control of the Organocatalytic Enantioselective α-Alkylation of Vinylogous Carbonyl Enolates for the Synthesis of Tetrahydropyran Derivatives and Beyond;Organic Letters;2021-05-28
3. Synthesis of Highly Functionalized Hydrindanes via Sequential Organocatalytic Michael/Mukaiyama Aldol Addition and Telescoped Hydrozirconation/Cross-Coupling as Key Steps: En Route to the AB System of Clifednamides;The Journal of Organic Chemistry;2021-05-20
4. New Developments of the Principle of Vinylogy as Applied to π-Extended Enolate-Type Donor Systems;Chemical Reviews;2020-02-10
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