Direct organocatalytic hydroalkoxylation of α,β-unsaturated ketones

dc.contributor.author Ramachary, Dhevalapally B.
dc.contributor.author Mondal, Rumpa
dc.date.accessioned 2022-03-27T09:42:07Z
dc.date.available 2022-03-27T09:42:07Z
dc.date.issued 2006-10-30
dc.description.abstract The direct addition of a variety of alcohols to in situ activated olefins was observed in the presence of mild bifunctional amine/acid catalysts. Unlike existing methods, the reactions proceed at room temperature and in the absence of transition metals. The use of simple commercially available catalysts, amines and acids makes this an attractive method for the preparation of β-alkoxy ketones, which are prevalent targets and intermediates in organic synthesis. © 2006 Elsevier Ltd. All rights reserved.
dc.identifier.citation Tetrahedron Letters. v.47(44)
dc.identifier.issn 00404039
dc.identifier.uri 10.1016/j.tetlet.2006.08.134
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/S0040403906017643
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13213
dc.subject Amine/acid catalysts
dc.subject Amino acids
dc.subject Enones
dc.subject Hydroalkoxylation
dc.subject Organocatalysis
dc.title Direct organocatalytic hydroalkoxylation of α,β-unsaturated ketones
dc.type Journal. Article
dspace.entity.type
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