ArticleBeilstein journal of organic chemistry2012
Organocatalytic tandem Michael addition reactions: A powerful access to the enantioselective synthesis of functionalized chromenes, thiochromenes and 1,2-dihydroquinolines.
Article in Beilstein journal of organic chemistry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed.
- Uncover the strength of polyhedral dicarbaboranes as the next generation of superbases in organocatalysis.Nature communications · 2026Article
- Doubly Decarboxylative Synthesis of 4-(Pyridylmethyl)chroman-2-ones and 2-(Pyridylmethyl)chroman-4-ones under Mild Reaction Conditions.Molecules (Basel, Switzerland) · 2021Article
- Synthesis of 4-Substituted-1,2-Dihydroquinolines by Means of Gold-Catalyzed Intramolecular Hydroarylation Reaction ofMolecules (Basel, Switzerland) · 2021Article
- A bifunctional iminophosphorane squaramide catalyzed enantioselective synthesis of hydroquinazolinesChemical science · 2021Article
- Dihydroquinolines, Dihydronaphthyridines and Quinolones by Domino Reactions of Morita-Baylis-Hillman Acetates.Molecules (Basel, Switzerland) · 2021Article
- Recent advances in organocatalytic asymmetric aza-Michael reactions of amines and amides.Beilstein journal of organic chemistry · 2021Review
- Isothiourea-catalysed enantioselective Michael addition of N-heterocyclic pronucleophiles to α,β-unsaturated aryl esters.Chemical science · 2019Article
- Direct allylic C-H alkylation of enol silyl ethers enabled by photoredox-Brønsted base hybrid catalysis.Nature communications · 2019Article
- Article
- Primary-tertiary diamine-catalyzed Michael addition of ketones to isatylidenemalononitrile derivatives.Beilstein journal of organic chemistry · 2014Article
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4 authors.
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Abstract
Enantioselective organocatalysis has become a field of central importance within asymmetric chemical synthesis and appears to be efficient approach toward the construction of complex chiral molecules from simple achiral materials in one-pot transformations under mild conditions with high stereocontrol. This review addresses the most significant synthetic methods reported on chiral-amine-catalyzed tandem Michael conjugate addition of heteroatom-centered nucleophiles to α,β-unsaturated compounds followed by cyclization reactions for the enantioselective construction of functionalized chiral chromenes, thiochromenes and 1,2-dihydroquinolines in optically enriched forms found in a myriad of bioactive natural products and synthetic compounds.
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