Toward ideal carbon dioxide functionalization

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Toward ideal carbon dioxide functionalization. / Yang, Y.; Lee, Ji Woong.

I: Chemical Science, Bind 10, Nr. 14, 2019, s. 3905-3926.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Harvard

Yang, Y & Lee, JW 2019, 'Toward ideal carbon dioxide functionalization', Chemical Science, bind 10, nr. 14, s. 3905-3926. https://doi.org/10.1039/C8SC05539D

APA

Yang, Y., & Lee, J. W. (2019). Toward ideal carbon dioxide functionalization. Chemical Science, 10(14), 3905-3926. https://doi.org/10.1039/C8SC05539D

Vancouver

Yang Y, Lee JW. Toward ideal carbon dioxide functionalization. Chemical Science. 2019;10(14):3905-3926. https://doi.org/10.1039/C8SC05539D

Author

Yang, Y. ; Lee, Ji Woong. / Toward ideal carbon dioxide functionalization. I: Chemical Science. 2019 ; Bind 10, Nr. 14. s. 3905-3926.

Bibtex

@article{2758db4c14144cb2b515df8266c27680,
title = "Toward ideal carbon dioxide functionalization",
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 {\textquoteleft}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. ",
author = "Y. Yang and Lee, {Ji Woong}",
year = "2019",
doi = "10.1039/C8SC05539D",
language = "English",
volume = "10",
pages = "3905--3926",
journal = "Chemical Science",
issn = "2041-6520",
publisher = "Royal Society of Chemistry",
number = "14",

}

RIS

TY - JOUR

T1 - Toward ideal carbon dioxide functionalization

AU - Yang, Y.

AU - Lee, Ji Woong

PY - 2019

Y1 - 2019

N2 - 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.

AB - 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.

U2 - 10.1039/C8SC05539D

DO - 10.1039/C8SC05539D

M3 - Journal article

AN - SCOPUS:85064041229

VL - 10

SP - 3905

EP - 3926

JO - Chemical Science

JF - Chemical Science

SN - 2041-6520

IS - 14

ER -

ID: 222051237