Highly Z- and enantioselective ring-opening/cross-metathesis reactions and Z-selective ring-opening metathesis polymerization
Highly Z- and enantioselective ring-opening/cross-metathesis reactions and Z-selective ring-opening metathesis polymerization
Stopping the gap: A notable shortcoming in olefin metathesis chemistry was the lack of methods for the selective synthesis of Z?alkenes. A breakthrough has now been achieved by the employment of a new type of chiral Mo complex (see scheme; TBS=tert-butyldimethylsilyl, X=Cl, Br, I). The first examples of the titled reactions are discussed.
alkenes, asymmetric catalysis, enantioselectivity, metathesis, molybdenum
8827-8831
Córdova, Armando
d2a1239f-708d-4f9c-bf7c-c095e9a27cac
Rios, Ramon
609bedf2-e886-4d62-a676-a32b6f8c1441
9 November 2009
Córdova, Armando
d2a1239f-708d-4f9c-bf7c-c095e9a27cac
Rios, Ramon
609bedf2-e886-4d62-a676-a32b6f8c1441
Córdova, Armando and Rios, Ramon
(2009)
Highly Z- and enantioselective ring-opening/cross-metathesis reactions and Z-selective ring-opening metathesis polymerization.
Angewandte Chemie International Edition, 48 (47), .
(doi:10.1002/anie.200903409).
(PMID:19839020)
Abstract
Stopping the gap: A notable shortcoming in olefin metathesis chemistry was the lack of methods for the selective synthesis of Z?alkenes. A breakthrough has now been achieved by the employment of a new type of chiral Mo complex (see scheme; TBS=tert-butyldimethylsilyl, X=Cl, Br, I). The first examples of the titled reactions are discussed.
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e-pub ahead of print date: 16 October 2009
Published date: 9 November 2009
Keywords:
alkenes, asymmetric catalysis, enantioselectivity, metathesis, molybdenum
Organisations:
Chemistry
Identifiers
Local EPrints ID: 340217
URI: http://eprints.soton.ac.uk/id/eprint/340217
ISSN: 1433-7851
PURE UUID: 6a2f7c52-62ec-4003-b9dd-a12da2ef650e
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Date deposited: 15 Jun 2012 11:35
Last modified: 14 Mar 2024 11:20
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Author:
Armando Córdova
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