Highly syn-diastereoselective Michael addition of enolizable ketones to 3-(diethoxyphosphoryl)coumarin
Author:
Funder
National Science Centre Poland
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference30 articles.
1. The Enamine Alkylation and Acylation of Carbonyl Compounds
2. The Chemistry of Carbanions. XI. Michael Reactions with 2-Methylcyclopentanone and 2-Methylcyclohexanone1a
3. The First Michael Addition of Metal Ketone Enolates to α,β-Unsaturated Esters under Catalytic Conditions: Tin Enolate with a Catalytic Amount of Tetrabutylammonium Bromide
4. Michael Addition of Stannyl Ketone Enolate to α,β-Unsaturated Esters Catalyzed by Tetrabutylammonium Bromide and an ab Initio Theoretical Study of the Reaction Course
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3. Anticancer Properties of a New Hybrid Analog AD-013 Combining a Coumarin Scaffold with an α-methylene-δ-lactone Motif;Anti-Cancer Agents in Medicinal Chemistry;2018-06-04
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5. An efficient synthesis of 3-diethoxyphosphoryl-4-(1H-indol-3-yl)-3,4-dihydrocoumarins: a convenient approach to 3-methylene-4-(indol-3-yl)-3,4-dihydrocoumarins;Arkivoc;2018-01-28
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