Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/9090
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dc.contributor.authorBabu, Vommina V Suresh-
dc.contributor.authorKantharaju-
dc.date.accessioned2010-05-31T04:52:56Z-
dc.date.available2010-05-31T04:52:56Z-
dc.date.issued2005-05-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/9090-
dc.description1046-1053en_US
dc.description.abstractAn efficient synthesis of 2,4,5-trichlorophenyl-(9H-fluoren-9-ylmethoxycarbonylamino)methylcarbamates employing isocyanates derived from several Fmoc-amino acids has been described. All the carbamates made have been obtained as crystalline solids and are fully characterized by IR, 1H NMR, 13C NMR and mass spectrometry. They have been used as building blocks for the synthesis of several dipeptidyl urea esters. The coupling of carbamates with N,O-bis[trimethyl­silyl]amino acids resulted in Fmoc-protected dipeptide urea acids in good yield as well as purity. All the dipeptidyl urea esters and acids made have been well characterized.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt.Cl.7 C 07 Ken_US
dc.sourceIJC-B Vol.44B(05) [May 2005]en_US
dc.title2,4,5-Trichlorophenyl-(9H-fluoren-9-ylmethoxycarbonylamino)methylcarbamates: Synthesis, isolation, characterization and utility in the synthesis of dipeptidyl ureasen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.44B(05) [May 2005]

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