Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4861
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dc.contributor.authorBasawaraj R
dc.contributor.authorGoled S.N
dc.contributor.authorKalaskar G
dc.contributor.authorSangapure S.S.
dc.date.accessioned2020-06-12T15:05:27Z-
dc.date.available2020-06-12T15:05:27Z-
dc.date.issued2008
dc.identifier.citationIndian Journal of Heterocyclic Chemistry , Vol. 18 , 1 , p. 1 - 4en_US
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4861-
dc.description.abstractThe nucleophilic displacement reaction of 2-substituted-4-chlorobenzofuran [3,2-d] pyrimidines 4-5 with nucleophiles such as sodium methoxide, sodiumethoxide and thiourea furnished 2-substituted-4-methoxy/ethoxy benzofuro [3,2-d] pyrimidines 6-9 and 2-substituted-3,4-dihydro-4-thiobenzofuro [3,2-d] pyrimidines 10-11 respectively. All the synthesized compounds were characterized on the basis of analytical and spectral data. These compounds were screened for their antimicrobial activities.en_US
dc.titleReaction products of 2-substituted-4-chlorobenzofuro [3,2-d] pyrimidines and their antimicrobial activitiesen_US
dc.typeArticle
Appears in Collections:1. Journal Articles

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