b-nitro-a-amino acids as latent a,b-dehydro-a-amino acid residues in peptides

dc.contributor.authorCoghlan, Phillip
dc.contributor.authorEaston, Christopher
dc.date.accessioned2015-12-13T23:35:05Z
dc.date.issued1999
dc.date.updated2015-12-12T09:38:38Z
dc.description.abstractPeptides containing α,β-dehydro-α-amino acid residues are readily prepared by incorporating β-nitro-α-amino acids at the corresponding positions, followed by elimination of nitrous acid.
dc.identifier.issn0040-4039
dc.identifier.urihttp://hdl.handle.net/1885/93746
dc.publisherElsevier
dc.sourceTetrahedron Letters
dc.subjectKeywords: alpha amino acid; amino acid derivative; nitro derivative; peptide derivative; article; chemical reaction; chemical structure; peptide synthesis; precipitation; reaction analysis; stereochemistry Amino acids and derivatives; Elimination Reactions; Enamides; Nitro compounds
dc.titleb-nitro-a-amino acids as latent a,b-dehydro-a-amino acid residues in peptides
dc.typeJournal article
local.bibliographicCitation.lastpage4748
local.bibliographicCitation.startpage4745
local.contributor.affiliationCoghlan, Phillip, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationEaston, Christopher, College of Physical and Mathematical Sciences, ANU
local.contributor.authoremailu9500570@anu.edu.au
local.contributor.authoruidCoghlan, Phillip, u960646
local.contributor.authoruidEaston, Christopher, u9500570
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.description.refereedYes
local.identifier.absfor030499 - Medicinal and Biomolecular Chemistry not elsewhere classified
local.identifier.ariespublicationMigratedxPub25148
local.identifier.citationvolume40
local.identifier.doi10.1016/S0040-4039(99)00839-4
local.identifier.scopusID2-s2.0-0033581016
local.identifier.uidSubmittedByMigrated
local.type.statusPublished Version

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