Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3610
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dc.contributor.authorMALI, SACHITANAND M.en_US
dc.contributor.authorJADHAV, SANDIP V.en_US
dc.contributor.authorGOPI, HOSAHUDYA N.en_US
dc.date.accessioned2019-07-23T11:08:16Z
dc.date.available2019-07-23T11:08:16Z
dc.date.issued2012-05en_US
dc.identifier.citationChemical Communications, 48(56),7085-7087.en_US
dc.identifier.issn1359-7345en_US
dc.identifier.issn1364-548Xen_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3610-
dc.identifier.urihttps://doi.org/10.1039/C2CC32581Ken_US
dc.description.abstractA novel, ultrafast, mild and scalable amide bond formation strategy in methanol using simple thioacids and amines is described. The mechanism suggests that the coupling reactions are initially mediated by CuSO4·5H2O and subsequently catalyzed by in situ generated copper sulfide. The pure peptides were isolated in satisfactory yields in less than 5 minutes.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectChemistryen_US
dc.subject2012en_US
dc.titleCopper(ii) mediated facile and ultra fast peptide synthesis in methanolen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleChemical Communicationsen_US
dc.publication.originofpublisherForeignen_US
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