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Enantioselective incorporation of CO2: status and potential

Permanent link
https://hdl.handle.net/10037/13741
DOI
https://doi.org/10.1021/acscatal.7b02306
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Accepted manuscript version (PDF)
Date
2017-09-09
Type
Journal article
Tidsskriftartikkel
Peer reviewed

Author
Vaitla, Janakiram; Guttormsen, Yngve; Mannisto, Jere K.; Nova, Ainara; Repo, Timo; Bayer, Annette; Hopmann, Kathrin Helen
Abstract
CO2 is a promising and sustainable carbon feedstock for organic synthesis. New catalytic protocols for efficient incorporation of CO2into organic molecules are continuously being reported. However, little progress has been made in the enantioselective conversion of CO2to form enantioenriched molecules. In order to allow CO2to become a versatile carbon source in academia and in the fine chemical and pharmaceutical industries, the development of enantioselective approaches is essential. Here we discuss general strategies for CO2activation and for generation of enantioenriched molecules, alongside selected examples of reactions involving asymmetric incorporation of CO2. The main product classes considered are carboxylic acids and derivatives (C–CO2bonds) and carbonates, carbamates, and polycarbonates (C–OCO bonds). Similarities to asymmetric hydrogenation are discussed, and some strategies for developing novel enantioselective CO2reactions are outlined.
Description
This document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS Catalysis, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acscatal.7b02306.
Publisher
American Chemical Society
Citation
Vaitla, J., Guttormsen, Y., Mannisto, J.K., Nova, A., Repo, T., Bayer, A. & Hopmann, K.H. (2017). Enantioselective incorporation of CO2: status and potential. ACS Catalysis, 7(10), 7231-7244. https://doi.org/10.1021/acscatal.7b02306
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