A new synthetic approach to the lactol moiety of halichoblelide

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dc.contributor.authorSantos, David
dc.contributor.authorAriza Piquer, Xavier
dc.contributor.authorGarcía Gómez, Jordi
dc.contributor.authorSánchez Zarzalejo, Carolina
dc.date.accessioned2017-11-09T15:43:09Z
dc.date.available2017-11-09T15:43:09Z
dc.date.issued2011
dc.date.updated2017-11-09T15:43:09Z
dc.description.abstractA stereoselective approach to the γ-lactol moiety of halichoblelide is described starting from commercially available (R)-1-butyn-3-ol. The key step is the hydroboration of a chiral protected 1,2-butadien-3-ol and its addition to furfural.
dc.format.extent5 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec594777
dc.identifier.issn0040-4020
dc.identifier.urihttps://hdl.handle.net/2445/117586
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1016/j.tet.2011.05.055
dc.relation.ispartofTetrahedron, 2011, vol. 67, num. 29, p. 5184-5188
dc.relation.urihttps://doi.org/10.1016/j.tet.2011.05.055
dc.rights(c) Elsevier B.V., 2011
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.sourceArticles publicats en revistes (Química Inorgànica i Orgànica)
dc.subject.classificationSíntesi orgànica
dc.subject.classificationAldehids
dc.subject.otherOrganic synthesis
dc.subject.otherAldehydes
dc.titleA new synthetic approach to the lactol moiety of halichoblelide
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/acceptedVersion

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