Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2144
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dc.contributor.authorKumar, Mothukuri Ganeshen_US
dc.contributor.authorThombare, Varsha J.en_US
dc.contributor.authorBHAISARE, RUPAL DINESHen_US
dc.contributor.authorAdak, Aninditaen_US
dc.contributor.authorGOPI, HOSAHUDYA N.en_US
dc.date.accessioned2019-03-15T11:22:37Z
dc.date.available2019-03-15T11:22:37Z
dc.date.issued2015-01en_US
dc.identifier.citationEuropean Journal of Organic Chemistry, 2015(1), 135-141.en_US
dc.identifier.issn1434-193Xen_US
dc.identifier.issn1099-0690en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2144-
dc.identifier.urihttps://doi.org/10.1002/ejoc.201403237en_US
dc.description.abstractA facile synthesis of highly symmetrical tetrasubstituted pyrazines through simple aerial oxidation of β‐keto γ‐amino esters is reported. The scope of the reaction was examined by use of various amino acid side‐chain functional groups and peptides. The mild and efficient transformation of β‐keto γ‐amino esters into pyrazines may serve as an attractive strategy for self‐dimerization of peptides.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectSynthesis of Tetrasubstituted Symmetricalen_US
dc.subjectγ‐Amino Estersen_US
dc.subjectMild Strategyen_US
dc.subjectSelf‐Dimerization of Peptidesen_US
dc.subjectHeterocyclic aromatic compoundsen_US
dc.subject2015en_US
dc.titleSynthesis of Tetrasubstituted Symmetrical Pyrazines from β‐Keto γ‐Amino Esters: A Mild Strategy for Self‐Dimerization of Peptidesen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleEuropean Journal of Organic Chemistryen_US
dc.publication.originofpublisherForeignen_US
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