dc.contributor.author | González Soengas, Raquel | |
dc.contributor.author | Rodríguez Solla, Humberto | |
dc.date.accessioned | 2021-02-04T11:39:47Z | |
dc.date.available | 2021-02-04T11:39:47Z | |
dc.date.issued | 2021 | |
dc.identifier.citation | Molecules, 26, 249, p. 1-40 (2021); doi:10.3390/molecules26020249 | |
dc.identifier.issn | 1420-3049 | |
dc.identifier.uri | http://hdl.handle.net/10651/57745 | |
dc.description.abstract | The 1,3-butadiene motif is widely found in many natural products and drug candidates with relevant biological activities. Moreover, dienes are important targets for synthetic chemists, due to their ability to give access to a wide range of functional group transformations, including a broad range of C-C bond-forming processes. Therefore, the stereoselective preparation of dienes have attracted much attention over the past decades, and the search for new synthetic protocols continues unabated. The aim of this review is to give an overview of the diverse methodologies that have emerged in the last decade, with a focus on the synthetic processes that meet the requirements of efficiency and sustainability of modern organic chemistry. | spa |
dc.description.sponsorship | Principado de Asturias (FICYT IDI/2018/000181)
European Union (European Regional Development Fund-ERDF)
MINECO (PID2019-109253RB-I00)
Arcelor Mittal (R&D-Principado de Asturias; FUO-20-296) | spa |
dc.format.extent | p. 1-40 | spa |
dc.language.iso | eng | spa |
dc.relation.ispartof | Molecules, 26(2) | spa |
dc.rights | CC Reconocimiento 4.0 Internacional | |
dc.rights | © 2021 los autores | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.subject | 1,3-dienes | spa |
dc.subject | Dienylation | |
dc.subject | Cross-coupling | |
dc.subject | Olefin metathesis | |
dc.title | Modern Synthetic Methods for the Stereoselective Construction of 1,3-Dienes | spa |
dc.type | info:eu-repo/semantics/article | spa |
dc.identifier.doi | 10.3390/molecules26020249 | |
dc.type.dcmi | text | spa |
dc.relation.projectID | FICYT IDI/2018/000181 | spa |
dc.relation.projectID | PID2019-109253RB-I00 | spa |
dc.relation.projectID | FUO-20-296 | spa |
dc.relation.publisherversion | https://doi.org/10.3390/molecules26020249 | |
dc.rights.accessRights | info:eu-repo/semantics/openAccess | |
dcterms.isPartOf | Molecules | |
dc.type.hasVersion | VoR | |