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dc.contributor.authorVANGALA, MADHURIen_US
dc.contributor.authorShinde, Ganesh P.en_US
dc.date.accessioned2019-04-29T10:14:36Z
dc.date.available2019-04-29T10:14:36Z
dc.date.issued2016-09en_US
dc.identifier.citationBeilstein Journal of Organic Chemistry, 12(1), 2086-2092.en_US
dc.identifier.issn1860-5397en_US
dc.identifier.issn1860-5397en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2675-
dc.identifier.urihttps://doi.org/10.3762/bjoc.12.197en_US
dc.description.abstractThe amidine bases DBU (1,8-diazabicyclo[5.4.0]undec-7-ene) and DBN (1,5-diazabicyclo[4.3.0]non-5-ene) display nucleophilic behaviour towards highly electrophilic p-nitrophenyl carbonate derivatives with ring opening of the bicyclic ring to form corresponding substituted ε-caprolactam and γ-lactam derived carbamates. This simple method presents a unified strategy to synthesize structurally diverse ε-caprolactam and γ-lactam compounds with a large substrate scope.en_US
dc.language.isoenen_US
dc.publisherBeilstein-Instituteen_US
dc.subjectCarbonatesen_US
dc.subjectDBNen_US
dc.subjectDBUen_US
dc.subjectlactamsen_US
dc.subjectp-nitrophenylen_US
dc.subjectOrganic basesen_US
dc.subject2016en_US
dc.titlep-Nitrophenyl carbonate promoted ring-opening reactions of DBU and DBN affording lactam carbamatesen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleBeilstein Journal of Organic Chemistryen_US
dc.publication.originofpublisherForeignen_US
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