dc.contributorUniv St Andrews
dc.contributorUniversidade Federal de São Paulo (UNIFESP)
dc.creatorTurnbull, W. B.
dc.creatorHarrison, J. A.
dc.creatorKartha, KPR
dc.creatorSchenkman, S.
dc.creatorField, R. A.
dc.date.accessioned2016-01-24T12:33:21Z
dc.date.accessioned2023-09-04T18:29:38Z
dc.date.available2016-01-24T12:33:21Z
dc.date.available2023-09-04T18:29:38Z
dc.date.created2016-01-24T12:33:21Z
dc.date.issued2002-04-15
dc.identifierTetrahedron. Oxford: Pergamon-Elsevier B.V., v. 58, n. 16, p. 3207-3216, 2002.
dc.identifier0040-4020
dc.identifierhttp://repositorio.unifesp.br/handle/11600/26833
dc.identifier10.1016/S0040-4020(02)00265-X
dc.identifierWOS:000175933700011
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/8615330
dc.description.abstractA comparison of chemical and chemo-enzymatic syntheses of alpha-2,3-sialylated octyl lactoside is reported. the chemical approach, starting from lactose and sialic acid, required 14 steps and proceeded in 5% overall yield; poor a-selectivity in the sialylation step necessitated a difficult and low yielding separation of anomers. A chemoenzymatic approach, employing recombinant Trypanosoma cruzi trans-sialidase to effect the key sialylation reaction, required 10 steps and gave a similar overall yield. Whereas the chemo-enzymatic synthesis required only three chromatographic purification steps overall, the chemical synthesis required at least nine. (C) 2002 Elsevier B.V. All rights reserved.
dc.languageeng
dc.publisherElsevier B.V.
dc.relationTetrahedron
dc.rightshttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dc.rightsAcesso restrito
dc.subjecttrans-sialidase
dc.subjectsynthesis
dc.subjectbiotransformations
dc.titleObservations on chemical and enzymatic approaches to alpha-2,3-sialylated octyl beta-lactoside
dc.typeArtigo


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