Amine induced carbonylation of alkynes to cyclobutenediones using Fe < inf > 3 < /inf > (CO) < inf > 12 < /inf >

dc.contributor.author Rameshkumar, Chellappan
dc.contributor.author Periasamy, Mariappan
dc.date.accessioned 2022-03-27T09:10:06Z
dc.date.available 2022-03-27T09:10:06Z
dc.date.issued 2000-04-08
dc.description.abstract Iron carbonyl species, prepared in situ in THF using Fe3(CO)12, react with alkynes at 25°C, in the presence of certain amines, to give the corresponding cyclobutenediones in moderate to good yields (25-61%) after CuCl2·2H2O oxidation. (C) 2000 Elsevier Science Ltd.
dc.identifier.citation Tetrahedron Letters. v.41(15)
dc.identifier.issn 00404039
dc.identifier.uri 10.1016/S0040-4039(00)00247-1
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/S0040403900002471
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12524
dc.subject Alkynes
dc.subject Amines
dc.subject Carbonylation
dc.subject Cyclobutenediones
dc.title Amine induced carbonylation of alkynes to cyclobutenediones using Fe < inf > 3 < /inf > (CO) < inf > 12 < /inf >
dc.type Journal. Article
dspace.entity.type
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