Palladium-catalyzed nucleophilic allylic substitution of Morita–Baylis–Hillman adducts with enamines: Synthesis of 1,5-dicarbonyl compounds
Author:
Publisher
Elsevier BV
Subject
General Chemical Engineering,General Chemistry
Reference31 articles.
1. De Novo Synthesis of Multisubstituted Aryl Amines Using Alkene Cross Metathesis
2. Free-Radical Variant for the Synthesis of Functionalized 1,5-Diketones
3. Heteroaromatic Synthesis via Olefin Cross-Metathesis: Entry to Polysubstituted Pyridines
4. Modular Synthesis of Highly Substituted Pyridines via Enolate α-Alkenylation
5. Reactions of 1,5-Diketones with Ammonia and Its Derivatives. (Review)
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1. Unveiling the abnormal effect of temperature on enantioselectivity in the palladium-mediated decabonylative alkylation of MBH acetate;Organic Chemistry Frontiers;2021
2. Addition Reactions;Organic Reaction Mechanisms Series;2020-07-24
3. First Zinc Bromide Promoted Annulative Domino Reactions between Enamines and Cyclic Morita–Baylis–Hillman Alcohols: Synthesis of N,O-Ketals;Synlett;2020-04-06
4. Bi(OTf)3-catalysed regioselective arylation of Morita-Baylis-Hillman type allylic electrophiles;Tetrahedron Letters;2020-04
5. Palladium-Catalyzed Allylic Substitution Reaction of Benzothiazolylacetamide with Allylic Alcohols in Water;The Journal of Organic Chemistry;2019-07-25
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