Asymmetric synthesis of (2S,3S)- and (2R,3S)-2,3-diaminobutanoic acids, non-protein amino-acid diastereomers found in a number of peptide antibiotics

(2S,3S)- and (2R,3S)-2,3-diaminobutanoic acids (DABA) are uncommon, naturally occurring amino acid diastereomers found as components of a number of peptide antibiotics. These 2,3-diamino acids have been synthesised by direct and indirect routes, with addition of a chiral lithium amide to tert-butyl...

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Autores principales: Burke, A, Davies, S, Hedgecock, C
Formato: Journal article
Publicado: 1996
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author Burke, A
Davies, S
Hedgecock, C
author_facet Burke, A
Davies, S
Hedgecock, C
author_sort Burke, A
collection OXFORD
description (2S,3S)- and (2R,3S)-2,3-diaminobutanoic acids (DABA) are uncommon, naturally occurring amino acid diastereomers found as components of a number of peptide antibiotics. These 2,3-diamino acids have been synthesised by direct and indirect routes, with addition of a chiral lithium amide to tert-butyl crotonate as a key step.
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spelling oxford-uuid:220d7bc9-28ee-4273-a588-397ecc39cc212022-03-26T11:36:35ZAsymmetric synthesis of (2S,3S)- and (2R,3S)-2,3-diaminobutanoic acids, non-protein amino-acid diastereomers found in a number of peptide antibioticsJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:220d7bc9-28ee-4273-a588-397ecc39cc21Symplectic Elements at Oxford1996Burke, ADavies, SHedgecock, C(2S,3S)- and (2R,3S)-2,3-diaminobutanoic acids (DABA) are uncommon, naturally occurring amino acid diastereomers found as components of a number of peptide antibiotics. These 2,3-diamino acids have been synthesised by direct and indirect routes, with addition of a chiral lithium amide to tert-butyl crotonate as a key step.
spellingShingle Burke, A
Davies, S
Hedgecock, C
Asymmetric synthesis of (2S,3S)- and (2R,3S)-2,3-diaminobutanoic acids, non-protein amino-acid diastereomers found in a number of peptide antibiotics
title Asymmetric synthesis of (2S,3S)- and (2R,3S)-2,3-diaminobutanoic acids, non-protein amino-acid diastereomers found in a number of peptide antibiotics
title_full Asymmetric synthesis of (2S,3S)- and (2R,3S)-2,3-diaminobutanoic acids, non-protein amino-acid diastereomers found in a number of peptide antibiotics
title_fullStr Asymmetric synthesis of (2S,3S)- and (2R,3S)-2,3-diaminobutanoic acids, non-protein amino-acid diastereomers found in a number of peptide antibiotics
title_full_unstemmed Asymmetric synthesis of (2S,3S)- and (2R,3S)-2,3-diaminobutanoic acids, non-protein amino-acid diastereomers found in a number of peptide antibiotics
title_short Asymmetric synthesis of (2S,3S)- and (2R,3S)-2,3-diaminobutanoic acids, non-protein amino-acid diastereomers found in a number of peptide antibiotics
title_sort asymmetric synthesis of 2s 3s and 2r 3s 2 3 diaminobutanoic acids non protein amino acid diastereomers found in a number of peptide antibiotics
work_keys_str_mv AT burkea asymmetricsynthesisof2s3sand2r3s23diaminobutanoicacidsnonproteinaminoaciddiastereomersfoundinanumberofpeptideantibiotics
AT daviess asymmetricsynthesisof2s3sand2r3s23diaminobutanoicacidsnonproteinaminoaciddiastereomersfoundinanumberofpeptideantibiotics
AT hedgecockc asymmetricsynthesisof2s3sand2r3s23diaminobutanoicacidsnonproteinaminoaciddiastereomersfoundinanumberofpeptideantibiotics