A formal, stereoselective synthesis of the natural tetrahydropyran derivative ophiocerin D

dc.contributor.author	Paños Pérez, Julián
dc.contributor.author	Murga, Juan
dc.contributor.author	Falomir, Eva
dc.contributor.author	Carda, Miguel
dc.contributor.author	Marco, J. Alberto
dc.date.accessioned	2012-10-22T11:17:39Z
dc.date.available	2012-10-22T11:17:39Z
dc.date.issued	2010
dc.identifier	http://dx.doi.org/10.1016/j.tetasy.2010.01.013
dc.identifier.citation	Tetrahedron Asymmetry, 21, 4, p. 425-428
dc.identifier.issn	9574166
dc.identifier.uri	http://hdl.handle.net/10234/49410
dc.description.abstract	A short, formal stereoselective synthesis of the naturally occurring tetrahydropyran derivative ophiocerin D is reported. The four stereocenters of the molecule were created with the aid of two Sharpless asymmetric dihydroxylations. © 2010 Elsevier Ltd. All rights reserved.
dc.language.iso	eng
dc.publisher	Elsevier
dc.rights.uri	http://rightsstatements.org/vocab/CNE/1.0/	*
dc.title	A formal, stereoselective synthesis of the natural tetrahydropyran derivative ophiocerin D
dc.type	info:eu-repo/semantics/article
dc.identifier.doi	http://dx.doi.org/10.1016/j.tetasy.2010.01.013
dc.rights.accessRights	info:eu-repo/semantics/restrictedAccess

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