Application of Enantiopure 1-(Aminoalkyl)naphthols and 2-(Aminoalkyl)phenols in the Enantioselective Addition of Organozinc to α,β-Unsaturated Carbonyl Compounds
Author:
Affiliation:
1. a University of Camerino, Department of Chemical Sciences , Camerino, Italy
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/00397910902737148
Reference20 articles.
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2. Enantioselektive 1,4-Additionen von metallorganischen Verbindungen an konjugierte Systeme im chiralen Medium DDB
3. Ligand effects in enantioface differentiating 1,4 addition to 1,3 diphenyl-2 propen-1 one
4. A new chiral ligand for the asymmetric conjugate addition of organocopper reagents to enones
5. Recent Advances in Catalytic Enantioselective Michael Additions
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1. Transition Metal‐Catalyzed Transformations of Chalcones;The Chemical Record;2024-07-15
2. Alkylation of Electron‐Deficient Olefins through Conjugate Addition of Organozinc Reagents: An Update;European Journal of Organic Chemistry;2021-09-08
3. Recent advances in the synthesis and synthetic applications of Betti base (aminoalkylnaphthol) and bis-Betti base derivatives;RSC Advances;2019
4. Formation of Aldehydes and Ketones by 1,4‐Addition to α,β‐Unsaturated Carbonyl Compounds and Derivatives;Comprehensive Organic Transformations;2018-02-28
5. Graphene oxide mediated solvent-free three component reaction for the synthesis of 1-amidoalkyl-2-naphthols and 1,2-dihydro-1-arylnaphth[1,2- e ][1,3]oxazin-3-ones;Tetrahedron Letters;2016-10
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