4.4 Review

Enantioselective desymmetrization reactions in asymmetric catalysis

Journal

TETRAHEDRON
Volume 106, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2022.132629

Keywords

Desymmetrization; meso-Compounds; Organocatalysis; Metal-catalysis; Biocatalysis

Funding

  1. Spanish Ministerio de Economia y Competitividad (MINECO) [CTQ2016-81797-REDC, CTQ2017-85093-P]
  2. Ministerio de Ciencia, Innovaci~on y Universidades [RED2018-102387-T, PID2019107268 GB-100]
  3. FEDER
  4. Generalitat Valenciana [IDIFEDER/2021/013, CIDEGENT/2020/058]
  5. University of Alicante [VIGROB-068]

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This review summarizes the recent advancements in enantioselective desymmetrization reactions using metal-catalyzed, organocatalyzed, and enzymatic processes. These asymmetric strategies have been successfully applied to a wide range of organic compounds, including diarylalkanes, silanes, alcohols, amines, and unsaturated compounds. The classical desymmetrization of various compounds by acylation, alkylation, and oxidation methods are important processes in organic synthesis. Desymmetrization methodologies have also been applied to small ring carbocycles and heterocyclic systems. The synthetic applications of these strategies in the total synthesis of natural products and biologically active compounds are highlighted.
This review covers the recent developments (since 2015) of enantioselective desymmetrization reactions using metal-catalyzed, organocatalyzed and enzymatic processes of prochiral and meso-compounds. This asymmetric strategy has been applied to a great number of organic compounds such as diarylalkanes, silanes, alcohols, amines and dibenzylmethylamines, as well as unsaturated compounds comprising dienes, diynes and cyclohexenes. The classical desymmetrization of 1,2-, 1,3-diols and other polyols by inter- and intramolecular acylation and alkylation reactions, but also by oxidation methods are important processes. Carbonyl compounds such as cycloalkanones, cyclohexadienones, cyclic and acyclic 1,3-diketones, cyclic 1,4-diketones are desymmetrized and applied to the synthesis of a wide range of natural products. In the case of dicarboxylic acid derivatives, diesters and lactones, anhydrides, diamides and dinitriles are mainly desymmetrized by intra- and intermolecular esterifications and hydrolysis. Small ring carbocycles such as cyclopropanes and cyclopropenes, cyclobutanes and cyclobutenes, and also cyclopentanes and cyclopentenes, cyclohexanes and cyclohexenes are considered. Heterocyclic systems such as small ring oxygen containing epoxides, oxetanes and oxabenzonorbornadienes as well as nitrogen containing aziridines, azetidines, azabenzonorbornadienes and diazanorbornenes are desymmetrized mainly by asymmetric ring opening reactions. The synthetic applications of these desymmetrization methodologies in the total synthesis of natural products and biologically active compounds are highlighted. (C) 2022 Published by Elsevier Ltd.

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