Stereoselective syntheses of the glycosidase inhibitors hyacinthacine A2, hyacinthacine A3 and 5-epi-hyacinthacine A3

dc.contributor.author	Ribés Vidal, Celia
dc.contributor.author	Falomir, Eva
dc.contributor.author	Carda, Miguel
dc.contributor.author	Marco, J. Alberto
dc.date.accessioned	2012-08-07T09:55:53Z
dc.date.available	2012-08-07T09:55:53Z
dc.date.issued	2009
dc.identifier	http://dx.doi.org/10.1016/j.tet.2009.06.046
dc.identifier.citation	Tetrahedron, 65, 34, p. 6965-6971
dc.identifier.issn	404020
dc.identifier.uri	http://hdl.handle.net/10234/43709
dc.description.abstract	Stereoselective syntheses of the naturally occurring glycosidase inhibitors hyacinthacines A2 and A3 are reported. In the case of hyacinthacine A2, the pyrrolizidine system was created from an acyclic precursor via a double cyclization procedure with a one-pot formation of two C-N bonds. In the case of hyacinthacine A3, the two C-N bonds were created in separate steps. In addition, the non-natural epimer at C-5 of hyacinthacine A3 was obtained.
dc.language.iso	eng
dc.publisher	Elsevier
dc.rights.uri	http://rightsstatements.org/vocab/CNE/1.0/	*
dc.title	Stereoselective syntheses of the glycosidase inhibitors hyacinthacine A2, hyacinthacine A3 and 5-epi-hyacinthacine A3
dc.type	info:eu-repo/semantics/article
dc.identifier.doi	http://dx.doi.org/10.1016/j.tet.2009.06.046
dc.rights.accessRights	info:eu-repo/semantics/restrictedAccess

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