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dc.contributor.authorSakhuja, Rajeev-
dc.date.accessioned2021-11-11T11:02:26Z-
dc.date.available2021-11-11T11:02:26Z-
dc.date.issued2009-03-18-
dc.identifier.urihttps://pubs.acs.org/doi/10.1021/jo900066m-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3394-
dc.description.abstract2H-Chromene-based conjugates of N-acyl-1,ω-amino acids (5, 9a−f, 14a−f) of natural amino acids (10a,b) and of dipeptide (10c) are prepared (60−97%) by N-acylbenzotriazole methodology in aqueous media at 20 °C. Gelation properties of the corresponding sodium salts in DMF and DMSO are generalized with respect to an increase or decrease in the chain length of the spacer.en_US
dc.language.isoenen_US
dc.publisherACSen_US
dc.subjectChemistryen_US
dc.subjectPeptides and proteinsen_US
dc.subjectMonomersen_US
dc.subjectGelationen_US
dc.titleGelation Behavior of 2H-Chromene N-Acylamino Acid Conjugatesen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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