Stereoselective synthesis of the naturally occurring 2-pyranone dodoneine

dc.contributor.author	Álvarez Bercedo, Paula
dc.contributor.author	Falomir, Eva
dc.contributor.author	Murga, Juan
dc.contributor.author	Carda, Miguel
dc.contributor.author	Marco, J. Alberto
dc.date.accessioned	2011-05-12T10:28:59Z
dc.date.available	2011-05-12T10:28:59Z
dc.date.issued	2008-08
dc.identifier.citation	ÁLVAREZ BERCEDO, Laura; FALOMIR, Eva; MURGA, Juan; CARDA, Miguel; MARCO, J. Alberto. Stereoselective synthesis of the naturally occurring 2-pyranone dodoneine. European journal of organic chemistry, 2008, no. 23, p. 4015-4018
dc.identifier.issn	1434-193X
dc.identifier.uri	http://hdl.handle.net/10234/22304
dc.description.abstract	The first total synthesis of the naturally occurring dihydropyranone dodoneine is reported. Asymmetric allylations were used for the stereoselective generation of the two stereogenic centers. The pyranone ring was created by means of a ringclosing metathesis
dc.format.extent	5 p.
dc.language.iso	eng
dc.publisher	Wiley-VCH
dc.relation.isPartOf	European journal of organic chemistry, 2008, no. 23
dc.rights.uri	http://rightsstatements.org/vocab/CNE/1.0/	*
dc.subject	Dodoneine
dc.subject	Oxygen heterocycles
dc.subject	5,6-Dihydropyran-2-ones
dc.subject	Allylation
dc.subject	Asymmetric synthesis
dc.subject	Ring-closing metathesis
dc.title	Stereoselective synthesis of the naturally occurring 2-pyranone dodoneine
dc.type	info:eu-repo/semantics/article
dc.rights.accessRights	info:eu-repo/semantics/openAccess