| dc.creator | Argüello, Juan Elias | |
| dc.creator | Pérez-Ruiz, Raúl | |
| dc.creator | Miranda, Miguel A. | |
| dc.date.accessioned | 2019-02-19T17:54:17Z | |
| dc.date.accessioned | 2022-10-15T13:11:15Z | |
| dc.date.available | 2019-02-19T17:54:17Z | |
| dc.date.available | 2022-10-15T13:11:15Z | |
| dc.date.created | 2019-02-19T17:54:17Z | |
| dc.date.issued | 2010-04 | |
| dc.identifier | Argüello, Juan Elias; Pérez-Ruiz, Raúl; Miranda, Miguel A.; Photoinduced electron-transfer cycloreversion of thietanes: The role of ion-molecule complexes; American Chemical Society; Organic Letters; 12; 8; 4-2010; 1884-1887 | |
| dc.identifier | 1523-7060 | |
| dc.identifier | http://hdl.handle.net/11336/70441 | |
| dc.identifier | 1523-7052 | |
| dc.identifier | CONICET Digital | |
| dc.identifier | CONICET | |
| dc.identifier.uri | https://repositorioslatinoamericanos.uchile.cl/handle/2250/4389889 | |
| dc.description.abstract | Cycloreversion (CR) of thietane radical cations leads to formation of thiobenzophenone and the corresponding alkenes, eventually followed by secondary [4 + 2] cycloaddition. Final product distribution depends on the ability of fragments to escape from ion-molecule complexes (IMCs). | |
| dc.language | eng | |
| dc.publisher | American Chemical Society | |
| dc.relation | info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1021/ol100520m | |
| dc.relation | info:eu-repo/semantics/altIdentifier/url/https://pubs.acs.org/doi/abs/10.1021/ol100520m | |
| dc.rights | https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ | |
| dc.rights | info:eu-repo/semantics/restrictedAccess | |
| dc.subject | electron transfer | |
| dc.subject | photochemistry | |
| dc.subject | thietanes | |
| dc.title | Photoinduced electron-transfer cycloreversion of thietanes: The role of ion-molecule complexes | |
| dc.type | info:eu-repo/semantics/article | |
| dc.type | info:ar-repo/semantics/artículo | |
| dc.type | info:eu-repo/semantics/publishedVersion | |