Applications of Baylis-Hillman acetates: One-pot, facile and convenient synthesis of substituted γ-lactams

dc.contributor.author Basavaiah, Deevi
dc.contributor.author Rao, Jamjanam Srivardhana
dc.date.accessioned 2022-03-27T09:02:27Z
dc.date.available 2022-03-27T09:02:27Z
dc.date.issued 2004-02-16
dc.description.abstract A simple, convenient and one-pot transformation of the acetates of Baylis-Hillman adducts into substituted γ-lactams, that is, (E)-5-alkyl-3-arylidenepyrrolidin-2-ones via treatment with nitroalkanes in the presence of a base, followed by reductive cyclization, using Fe/AcOH, is described. © 2004 Elsevier Ltd. All rights reserved.
dc.identifier.citation Tetrahedron Letters. v.45(8)
dc.identifier.issn 00404039
dc.identifier.uri 10.1016/j.tetlet.2003.12.133
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/S0040403904000371
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12314
dc.subject Baylis-Hillman chemistry
dc.subject Fe/AcOH
dc.subject Reductive cyclization
dc.subject γ-Lactams
dc.title Applications of Baylis-Hillman acetates: One-pot, facile and convenient synthesis of substituted γ-lactams
dc.type Journal. Article
dspace.entity.type
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