Toward ideal carbon dioxide functionalization

Y. Yang, Ji Woong Lee*

*Corresponding author af dette arbejde

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

142 Citationer (Scopus)
551 Downloads (Pure)

Abstract

This Perspective recapitulates recent developments of carbon dioxide utilization in carbon-carbon bond formation reactions, with an intention of paving a way toward sustainable CO 2 -functionalization and its tangible applications in synthetic chemistry. CO 2 functionalization reactions possess intrinsic drawbacks: the high kinetic inertness and thermodynamic stability of CO 2 . Numerous procedures for CO 2 utilization depend on energy-intensive processes (i.e. high pressure and/or temperature), often solely relying on reactive substrates, hampering its general applications. Recent efforts thus have been dedicated to catalytic CO 2 -utilization under ambient reaction conditions, however, it is still limited to a few activation modes and the use of reactive substrates. Herein, ideal CO 2 -functionalization with particular emphasis on sustainability will be discussed based on the following sub-categories; (1) metal-catalyzed ‘reductive' carboxylation reaction of halides, olefins and allyl alcohols, (2) photochemical CO 2 -utilization, (3) redox-neutral CO 2 -functionalization, and (4) enantioselective catalysis incorporating CO 2 to form C-CO 2 bonds (excluding strain mediated reactions with epoxide- and aziridine-based substrates). Recent progress in these fields will be discussed with the proposed reaction mechanisms and selected examples, highlighting redox-neutral, umpolung, and asymmetric carboxylation to postulate ideal CO 2 functionalization reactions to be developed in the near future.

OriginalsprogEngelsk
TidsskriftChemical Science
Vol/bind10
Udgave nummer14
Sider (fra-til)3905-3926
Antal sider22
ISSN2041-6520
DOI
StatusUdgivet - 2019

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