AuCl < inf > 3 < /inf > /AgSbF < inf > 6 < /inf > -catalyzed rapid epoxide to carbonyl rearrangement

dc.contributor.author Gudla, Vanajakshi
dc.contributor.author Balamurugan, Rengarajan
dc.date.accessioned 2022-03-27T08:39:27Z
dc.date.available 2022-03-27T08:39:27Z
dc.date.issued 2012-09-26
dc.description.abstract An efficient epoxide to carbonyl rearrangement using catalytic AuCl 3/AgSbF 6 has been presented. The reactions are fast and high yielding. β-Hydrogen migration takes place exclusively when hydrogen and methyl or substituted methyl groups are present at β-carbon of epoxide. When phenyl/acetyl/benzoyl and hydrogen are available at same carbon atom, migration of the former is preferred over the latter. © 2012 Elsevier Ltd. All rights reserved.
dc.identifier.citation Tetrahedron Letters. v.53(39)
dc.identifier.issn 00404039
dc.identifier.uri 10.1016/j.tetlet.2012.07.056
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/S0040403912012312
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/11388
dc.subject Epoxides
dc.subject Gold catalysis
dc.subject Meinwald rearrangement
dc.subject Rearrangement
dc.title AuCl < inf > 3 < /inf > /AgSbF < inf > 6 < /inf > -catalyzed rapid epoxide to carbonyl rearrangement
dc.type Journal. Article
dspace.entity.type
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