| dc.contributor.author | Mato Santamaría, Raquel | |
| dc.contributor.author | Reyes Martín, Efraim | |
| dc.contributor.author | Carrillo Fernández, María Luisa  | |
| dc.contributor.author | Uria Pujana, Uxue | |
| dc.contributor.author | Prieto Aretxabaleta, Liher | |
| dc.contributor.author | Manzano, Rubén | |
| dc.contributor.author | Vicario Hernando, José Luis | |
| dc.date.accessioned | 2023-12-13T13:07:54Z | |
| dc.date.available | 2023-12-13T13:07:54Z | |
| dc.date.issued | 2020-09-28 | |
| dc.identifier.citation | Chemical Communications 56 : 13149-13152(2020) | es_ES |
| dc.identifier.issn | 1359-7345 | |
| dc.identifier.issn | 1364-548X (electronic) | |
| dc.identifier.uri | http://hdl.handle.net/10810/63359 | |
| dc.description.abstract | The enantioselective Michael reaction catalyzed by a bifunctional tertiary amine/squaramide has been used to trigger a Michael/transannular aldol cascade process that leads to densely substituted bicyclo[5.4.0]undecanes and in which three contiguous stereogenic centres, one of them a tertiary alcohol moiety, have been formed in a fully stereocontrolled fashion. | es_ES |
| dc.description.sponsorship | Spanish MICINN(FEDER-CTQ201783633-P), Basque Government (Grupos IT908-16 and fellowships to R.Mato and R.Manzano) | es_ES |
| dc.language.iso | eng | es_ES |
| dc.publisher | Royal Society of Chemistry | es_ES |
| dc.relation | info:eu-repo/grantAgreement/MICINN/CTQ201783633-P | es_ES |
| dc.rights | info:eu-repo/semantics/openAccess | es_ES |
| dc.title | Catalytic enantioselective domino Michael/transannular aldol reaction under bifunctional catalysis | es_ES |
| dc.type | info:eu-repo/semantics/article | es_ES |
| dc.rights.holder | © 2020, The Royal Society of Chemistry | es_ES |
| dc.relation.publisherversion | https://doi.org/10.1039/D0CC05981A | es_ES |
| dc.identifier.doi | 10.1039/D0CC05981A | |
| dc.departamentoes | Química orgánica II | es_ES |
| dc.departamentoeu | Kimika organikoa II | es_ES |
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