Lactone Enolates of Isochroman-3-ones and 2-Coumaranones: Quantification of Their Nucleophilicity in DMSO and Conjugate Additions to Chalcones
Author:
Affiliation:
1. Dipartimento di Chimica e Biologia “A. Zambelli”, Università degli Studi di Salerno, Via Giovanni Paolo II, 84084 Fisciano, SA, Italy
2. Department Chemie, Ludwig-Maximilians-Universität München, Butenandtstr. 5-13, 81377 München, Germany
Funder
Universit? degli Studi di Salerno
H2020 Marie Sklodowska-Curie Actions
Ministero dell'Universit? e della Ricerca
Publisher
American Chemical Society (ACS)
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.4c00277
Reference43 articles.
1. Acyclic stereoselection. 7. Stereoselective synthesis of 2-alkyl-3-hydroxy carbonyl compounds by aldol condensation
2. Enantioselective organocatalytic Michael addition of 2-arylacetates and 2-arylacetonitriles having an electron-withdrawing group to α,β-unsaturated aldehydes
3. Equilibrium CH acidity of organophosphorus compounds
4. Generation and Reactivity of C(1)‐Ammonium Enolates by Using Isothiourea Catalysis
5. Enantioselective α-Chlorination Reactions of in Situ Generated C1 Ammonium Enolates under Base-Free Conditions
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