Axially Chiral N-Oxide Catalysts for the Allylation and Crotylation of Aromatic Aldehydes: Exploiting Nonlinear Effects
| dc.contributor.author | Ramírez López, Pedro | |
| dc.contributor.author | Romero-Arenas, Antonio | |
| dc.contributor.author | Iglesias-Sigüenza, Javier | |
| dc.contributor.author | Fernández, Rosario | |
| dc.contributor.author | Ros, Abel | |
| dc.contributor.author | Lassaletta, José María | |
| dc.date.accessioned | 2025-07-29T09:17:35Z | |
| dc.date.available | 2025-07-29T09:17:35Z | |
| dc.date.issued | 2024 | |
| dc.description | We thank the Spanish MICINN (grants PID2019–106358GB- C21, PID2019–106358GB-C22, PID2022–137888NB-I00, PID-143230NB-I00; European FEDER funds and the Junta de Andaluciá (Grants P18-FR-3531, P18-FR-644, US-1262867) for financial support. | |
| dc.description.abstract | A new family of IAN-type amine N-oxides is presented as catalysts for the allylation and crotylation of aromatic aldehydes with allyltrichlorosilanes. These reactions exhibit a remarkably positive nonlinear effect which enables the utilization of the catalysts in subenantiopure form. As enantiopure catalysts are not required under this regime, the synthesis of these N-oxides is straightforward through catalytic asymmetric synthesis, avoiding lengthy synthesis from the chiral pool or resolution of diastereoisomers. Studies of the corresponding crotylation with Z- and E-crotylsilanes suggest that the reaction proceeds through a chair-like transition state. | |
| dc.description.department | Depto. de Química en Ciencias Farmacéuticas | |
| dc.description.faculty | Fac. de Farmacia | |
| dc.description.refereed | TRUE | |
| dc.description.sponsorship | Ministerio de Ciencia e Innovación (España) | |
| dc.description.sponsorship | Junta de Andalucía | |
| dc.description.sponsorship | European Commission | |
| dc.description.status | pub | |
| dc.identifier.citation | Romero‐Arenas A, Ramírez‐López P, Iglesias‐Sigüenza J, Fernández R, Ros A, Lassaletta JM. Axially Chiral N ‐Oxide Catalysts for the Allylation and Crotylation of Aromatic Aldehydes: Exploiting Nonlinear Effects. ChemCatChem 2024;16:e202400806. https://doi.org/10.1002/cctc.202400806. | |
| dc.identifier.doi | 10.1002/cctc.202400806 | |
| dc.identifier.officialurl | https://doi.org/10.1002/cctc.202400806 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14352/122845 | |
| dc.issue.number | 21 | |
| dc.journal.title | ChemCatChem | |
| dc.language.iso | eng | |
| dc.publisher | Wiley | |
| dc.relation.projectID | info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2019-106358GB-C21 | |
| dc.relation.projectID | info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2019-106358GB-C22 | |
| dc.relation.projectID | info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2021-2023/PID2022–137888NB-I00 | |
| dc.relation.projectID | info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2021-2023/PID2022–143230NB-I00 | |
| dc.rights | Attribution-NonCommercial 4.0 International | en |
| dc.rights.accessRights | open access | |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc/4.0/ | |
| dc.subject.cdu | 547 | |
| dc.subject.cdu | 544.47 | |
| dc.subject.keyword | Organocatalysis | |
| dc.subject.keyword | Nonlinear effects | |
| dc.subject.keyword | N-oxides | |
| dc.subject.keyword | Allylation | |
| dc.subject.keyword | Trichlorosilanes | |
| dc.subject.ucm | Ciencias | |
| dc.subject.ucm | Química | |
| dc.subject.ucm | Química orgánica (Química) | |
| dc.subject.ucm | Ciencias Biomédicas | |
| dc.subject.unesco | 23 Química | |
| dc.subject.unesco | 24 Ciencias de la Vida | |
| dc.subject.unesco | 2306 Química Orgánica | |
| dc.subject.unesco | 2210.01 Catálisis | |
| dc.title | Axially Chiral N-Oxide Catalysts for the Allylation and Crotylation of Aromatic Aldehydes: Exploiting Nonlinear Effects | |
| dc.type | journal article | |
| dc.type.hasVersion | VoR | |
| dc.volume.number | 16 | |
| dspace.entity.type | Publication | |
| relation.isAuthorOfPublication | 3c0528fd-f8e9-489f-ba0b-68c1273aac9f | |
| relation.isAuthorOfPublication.latestForDiscovery | 3c0528fd-f8e9-489f-ba0b-68c1273aac9f |
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