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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 |