Oxidative Coupling of (−)-Sclareol and Related Diols Leading to Oxepane Terpenoids

dc.contributor.author	Bouanou, Hanane
dc.contributor.author	Gil, Juan A.
dc.contributor.author	Alvarez-Manzaneda Roldán, Ramón Jesús
dc.contributor.author	Chahboun, Rachid
dc.contributor.author	Alvarez-Manzaneda, Enrique
dc.date.accessioned	2024-04-12T13:22:55Z
dc.date.available	2024-04-12T13:22:55Z
dc.date.issued	2016-09-30
dc.identifier.citation	J. Org. Chem. 2016, 81, 10002−10008	es_ES
dc.identifier.issn	0022-3263
dc.identifier.uri	http://hdl.handle.net/10835/16344
dc.description.abstract	Treatment of (−)-sclareol and related compounds with lead tetraacetate affords tetracyclic compounds bearing a 2,8- dioxabicyclo[5.2.0]nonane moiety with complete regio- and stereoselectivity. This process, which is also applicable to 1,5-diols with a similar substitution pattern, facilitates the development of efficient syntheses toward oxepane terpenoids, such as aplysistatin derivatives.	es_ES
dc.language.iso	en	es_ES
dc.publisher	American Chemical Society	es_ES
dc.title	Oxidative Coupling of (−)-Sclareol and Related Diols Leading to Oxepane Terpenoids	es_ES
dc.type	info:eu-repo/semantics/article	es_ES
dc.relation.publisherversion	http://dx.doi.org/10.1021/acs.joc.6b01834	es_ES
dc.rights.accessRights	info:eu-repo/semantics/openAccess	es_ES
dc.identifier.doi	10.1021/acs.joc.6b01834