Novel deoxy-selenylconduritols: chemoenzymatic synthesis and biological evaluation

dc.creatorBELLOMO, Ana
dc.creatorBERTUCCI, Ana
dc.creatorSTEFANI, Helio
dc.creatorVAZQUEZ, Alvaro
dc.creatorGONZALEZ, David
dc.date.accessioned2012-10-19T03:17:33Z
dc.date.accessioned2018-07-04T14:56:02Z
dc.date.available2012-10-19T03:17:33Z
dc.date.available2018-07-04T14:56:02Z
dc.date.created2012-10-19T03:17:33Z
dc.date.issued2009
dc.identifierTETRAHEDRON-ASYMMETRY, v.20, n.23, p.2673-2676, 2009
dc.identifier0957-4166
dc.identifierhttp://producao.usp.br/handle/BDPI/19681
dc.identifier10.1016/j.tetasy.2009.11.004
dc.identifierhttp://dx.doi.org/10.1016/j.tetasy.2009.11.004
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1616468
dc.description.abstractThe first synthesis of two selenyldeoxycyclitols (4-bromo-2-phenylselenyl conduritol F and 6-phenylselenylconduritol F) is reported via a chemoenzymatic enantioselective route. The key step of the synthesis is the selenolysis of a vinyl epoxide. The new compounds were evaluated for their capacity to inhibit the growth of different microorganisms using a modification of the agar diffusion technique with thin layer chromatography plates as support. (C) 2009 Elsevier Ltd. All rights reserved.
dc.languageeng
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD
dc.relationTetrahedron-asymmetry
dc.rightsCopyright PERGAMON-ELSEVIER SCIENCE LTD
dc.rightsrestrictedAccess
dc.titleNovel deoxy-selenylconduritols: chemoenzymatic synthesis and biological evaluation
dc.typeArtículos de revistas


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