Recent developments in enantioselective zinc-catalyzed transformations
| Autor: | Hélène Pellissier |
|---|---|
| Přispěvatelé: | Institut des Sciences Moléculaires de Marseille (ISM2), Aix Marseille Université (AMU)-École Centrale de Marseille (ECM)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS) |
| Jazyk: | angličtina |
| Rok vydání: | 2021 |
| Předmět: |
chemistry.chemical_element
Zinc Enantioselectivity Green catalysis 010402 general chemistry 01 natural sciences Catalysis Inorganic Chemistry Transition metal Aldol reaction Asymmetric catalysis Materials Chemistry Organic chemistry Physical and Theoretical Chemistry Chirality 010405 organic chemistry Enantioselective transformations [CHIM.ORGA]Chemical Sciences/Organic chemistry Enantioselective synthesis Transition metals [CHIM.CATA]Chemical Sciences/Catalysis 0104 chemical sciences chemistry Alkynylation Nitro Chirality (chemistry) |
| Zdroj: | Coordination Chemistry Reviews Coordination Chemistry Reviews, 2021, 439, pp.213926. ⟨10.1016/j.ccr.2021.213926⟩ Coordination Chemistry Reviews, Elsevier, 2021, 439, pp.213926. ⟨10.1016/j.ccr.2021.213926⟩ |
| ISSN: | 0010-8545 |
| DOI: | 10.1016/j.ccr.2021.213926⟩ |
| Popis: | International audience; This review collects the recent advances in the field of enantioselective zinc-catalyzed transformations, covering the literature since the beginning of 2015, illustrating the power of chiral green zinc catalysts to promote all types of reactions. A range of highly enantioselective reactions have been developed in the last six years, including cycloadditions, alkynylation/allylation reactions of carbonyl compounds and derivatives, additions of diorganozincs to carbonyl compounds and derivatives, Mannich reactions, (nitro)aldol reactions, other 1,2-nucleophilic additions to carbonyl compounds and derivatives, Michael additions, Friedel-Crafts reactions, reductions, a-functionalizations of carbonyl compounds, ringopening reactions, epoxidations, halolactonizations, domino/tandem reactions and miscellaneous reactions. |
| Databáze: | OpenAIRE |
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