Stereoselective Transformations of (+)-Abietic Acid into (+)-Vitedoin B and (+)-Negundoin A

dc.contributor.author	Tapia, Rubén
dc.contributor.author	Bouanou, Hanane
dc.contributor.author	Alvarez, Esteban
dc.contributor.author	Alvarez-Manzaneda Roldán, Ramón Jesús
dc.contributor.author	Chahboun, Rachid
dc.contributor.author	Alvarez-Manzaneda, Enrique
dc.date.accessioned	2024-04-12T13:27:37Z
dc.date.available	2024-04-12T13:27:37Z
dc.date.issued	2014-04-15
dc.identifier.citation	J. Org. Chem. 2014, 79, 4405−4413	es_ES
dc.identifier.issn	0022-3263
dc.identifier.uri	http://hdl.handle.net/10835/16350
dc.description.abstract	The first synthesis of spirolactone (+)-vitedoin B (14 steps, 8.0% global yield) and spiro enol ether (+)-negundoin A (19 steps, 3.7% global yield), via a nor-labdane acetoxy ester, has been achieved starting from commercial (+)-abietic acid.	es_ES
dc.language.iso	en	es_ES
dc.publisher	American Chemical Society	es_ES
dc.title	Stereoselective Transformations of (+)-Abietic Acid into (+)-Vitedoin B and (+)-Negundoin A	es_ES
dc.type	info:eu-repo/semantics/article	es_ES
dc.relation.publisherversion	https://pubs.acs.org/doi/10.1021/jo5003533	es_ES
dc.rights.accessRights	info:eu-repo/semantics/openAccess	es_ES
dc.identifier.doi	10.1021/jo5003533