Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5362
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dc.contributor.authorSangapure S.S
dc.contributor.authorMulagi S.M.
dc.date.accessioned2020-06-12T15:07:56Z-
dc.date.available2020-06-12T15:07:56Z-
dc.date.issued2000
dc.identifier.citationIndian Journal of Heterocyclic Chemistry , Vol. 10 , 1 , p. 27 - 30en_US
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5362-
dc.description.abstractThe condensation of 3-amino-2-benzofurancarbonitrile (I) with isocyanates and isothiocyanates gave 3-alkyl/aryl-4-iminobenzofuro [3,2-d] pyrimidine derivatives (II and IVa-e) which underwent Dimroth rearrangement in aq dimethyl formamide to yield 4-alkyl/arylamino-1,2-dihydro-2-oxo/mercaptobenzofuro [3,2-d] pyrimidine derivatives (III and Va-e). The biological activities of the title compounds have been described.en_US
dc.titleSynthesis of some biologically active 4-amino-1,2-dihydro-2-oxo/mercaptobenzofuro [3,2-d] pyrimidine derivatives via Dimroth rearrangementen_US
dc.typeArticle
Appears in Collections:1. Journal Articles

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