Enantioselective hydroacylation of olefins with rhodium catalysts
Over thirty years ago, James and Young reported the first enantioselective olefin hydroacylation by using rhodium catalysts. This viewpoint highlights the advances in this area, including 4-pentenal cyclisations, medium-ring syntheses, and intermolecular variants. Since James and Young's semina...
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Published in | Chemical communications (Cambridge, England) Vol. 5; no. 89; pp. 13645 - 13649 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
England
18.11.2014
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Subjects | |
Online Access | Get full text |
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Summary: | Over thirty years ago, James and Young reported the first enantioselective olefin hydroacylation by using rhodium catalysts. This viewpoint highlights the advances in this area, including 4-pentenal cyclisations, medium-ring syntheses, and intermolecular variants.
Since James and Young's seminal report on the kinetic resolution of 4-pentenals by hydroacylation, enantioselective methods have progressed to include 4-pentenal cyclisations, medium-ring syntheses, and intermolecular variants. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/c4cc02276a |