A new synthetic approach to the lactol moiety of halichoblelide

Santos, David; Ariza Piquer, Xavier; García Gómez, Jordi; Sánchez Zarzalejo, Carolina

Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/117586

Full metadata record

DC Field	Value	Language
dc.contributor.author	Santos, David	-
dc.contributor.author	Ariza Piquer, Xavier	-
dc.contributor.author	García Gómez, Jordi	-
dc.contributor.author	Sánchez Zarzalejo, Carolina	-
dc.date.accessioned	2017-11-09T15:43:09Z	-
dc.date.available	2017-11-09T15:43:09Z	-
dc.date.issued	2011	-
dc.identifier.issn	0040-4020	-
dc.identifier.uri	http://hdl.handle.net/2445/117586	-
dc.description.abstract	A 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.extent	5 p.	-
dc.format.mimetype	application/pdf	-
dc.language.iso	eng	-
dc.publisher	Elsevier B.V.	-
dc.relation.isformatof	Versió postprint del document publicat a: https://doi.org/10.1016/j.tet.2011.05.055	-
dc.relation.ispartof	Tetrahedron, 2011, vol. 67, num. 29, p. 5184-5188	-
dc.relation.uri	https://doi.org/10.1016/j.tet.2011.05.055	-
dc.rights	(c) Elsevier B.V., 2011	-
dc.source	Articles publicats en revistes (Química Inorgànica i Orgànica)	-
dc.subject.classification	Síntesi orgànica	-
dc.subject.classification	Aldehids	-
dc.subject.other	Organic synthesis	-
dc.subject.other	Aldehydes	-
dc.title	A new synthetic approach to the lactol moiety of halichoblelide	-
dc.type	info:eu-repo/semantics/article	-
dc.type	info:eu-repo/semantics/acceptedVersion	-
dc.identifier.idgrec	594777	-
dc.date.updated	2017-11-09T15:43:09Z	-
dc.rights.accessRights	info:eu-repo/semantics/openAccess	-
Appears in Collections:	Articles publicats en revistes (Química Inorgànica i Orgànica)

Files in This Item:

File	Description	Size	Format
594777.pdf		475.2 kB	Adobe PDF	View/Open

Show simple item record