Publication: Diverse methods with stereoselective induction in the asymmetric Biginelli reaction
| dc.contributor.author | Díaz Fernández, Marcos | |
| dc.contributor.author | Algarra González, Manuel | |
| dc.contributor.author | Calvo Losada, Saturnino | |
| dc.contributor.author | Quirante, José Joaquín | |
| dc.contributor.author | Sarabia, Francisco | |
| dc.contributor.author | Pino-González, María Soledad | |
| dc.contributor.department | Institute for Advanced Materials and Mathematics - INAMAT2 | en |
| dc.date.accessioned | 2024-10-03T11:37:49Z | |
| dc.date.available | 2024-10-03T11:37:49Z | |
| dc.date.issued | 2024-08-15 | |
| dc.date.updated | 2024-10-03T11:34:02Z | |
| dc.description.abstract | The relevance of the asymmetric Biginelli reaction (ABR) has been increased in this century, due to the pharmacological application of its products. This review focuses predominantly on articles published in the period from 2015 to 2024 on asymmetric synthetic advances in the formation of dihydropyrimidinones (DHPMs), dihydropyrimidinethiones (DHPMTs), and related compounds. The relevant bibliography on general processes in the Biginelli reaction and some methods of separation of isomers have also been referenced. | en |
| dc.description.sponsorship | Financial support has been received from the Spanish Ministry of Science and Innovation RTI2018-098296-BI00 (MINECO and FEDER), and M. Algarra would like to thank the Ministry of Science and Innovation (MCIN/AEI/https://doi.org/10.13039/501100011033) for their support under the grant number PID2021-122613OB-I00 | |
| dc.format.mimetype | application/pdf | |
| dc.identifier.citation | Díaz-Fernández, M., Algarra, M., Calvo-Losada, S., Quirante, J. J., Sarabia, F., Pino-González, M. S. (2024) Diverse methods with stereoselective induction in the asymmetric Biginelli reaction. Molecules, 29(16), 1-20. https://doi.org/10.3390/molecules29163864 | |
| dc.identifier.doi | 10.3390/molecules29163864 | |
| dc.identifier.issn | 1420-3049 | |
| dc.identifier.uri | https://academica-e.unavarra.es/handle/2454/51961 | |
| dc.language.iso | eng | |
| dc.publisher | MDPI Publishing | |
| dc.relation.ispartof | Molecules, 29(16), 1-20 | |
| dc.relation.projectID | info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/RTI2018-098296-BI00 | |
| dc.relation.projectID | info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2021-2023/PID2021-122613OB-I00/ES/ | |
| dc.relation.publisherversion | https://doi.org/10.3390/molecules29163864 | |
| dc.rights | © 2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license. | |
| dc.rights.accessRights | info:eu-repo/semantics/openAccess | |
| dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | |
| dc.subject | Pyrimidines | en |
| dc.subject | Multicomponent reactions | en |
| dc.subject | Asymmetric | en |
| dc.subject | Enantioselective | en |
| dc.subject | N-heterocycles | en |
| dc.subject | Biginelli reaction | en |
| dc.title | Diverse methods with stereoselective induction in the asymmetric Biginelli reaction | en |
| dc.type | info:eu-repo/semantics/article | |
| dc.type.version | info:eu-repo/semantics/publishedVersion | |
| dspace.entity.type | Publication | |
| relation.isAuthorOfPublication | ac68d8d5-2b22-478e-878b-bb0893409ddf | |
| relation.isAuthorOfPublication.latestForDiscovery | ac68d8d5-2b22-478e-878b-bb0893409ddf |