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| Campo DC | Valor | Lengua/Idioma |
|---|---|---|
| dc.provenance | CONICET | - |
| dc.creator | Kaufman, Teodoro Saul | - |
| dc.creator | Amongero, Marcela | - |
| dc.date | 2016-06-02T18:50:59Z | - |
| dc.date | 2016-06-02T18:50:59Z | - |
| dc.date | 2013-01-30 | - |
| dc.date | 2016-06-01T13:34:31Z | - |
| dc.date.accessioned | 2019-04-29T15:28:28Z | - |
| dc.date.available | 2019-04-29T15:28:28Z | - |
| dc.date.issued | 2016-06-02T18:50:59Z | - |
| dc.date.issued | 2016-06-02T18:50:59Z | - |
| dc.date.issued | 2013-01-30 | - |
| dc.date.issued | 2016-06-01T13:34:31Z | - |
| dc.identifier | Kaufman, Teodoro Saul; Amongero, Marcela; Synthesis of optically active 1,2,3-trisubstituted azetidines employing an organocatalytic approach with L-proline; Elsevier; Tetrahedron Letters; 54; 15; 30-1-2013; 1924-1927 | - |
| dc.identifier | 0040-4039 | - |
| dc.identifier | http://hdl.handle.net/11336/6022 | - |
| dc.identifier.uri | http://rodna.bn.gov.ar:8080/jspui/handle/bnmm/294772 | - |
| dc.description | A concise organocatalytic approach towards optically active 1,2,3-trisubstituted azetidines, including a study of the scope and limitations of the synthetic sequence, is reported. The synthesis comprises the one-pot L-proline promoted three-component reaction between substituted benzaldehydes, anilines and enolizable aldehydes, followed by the in situ reduction of the resulting b-aminoaldehydes to the corresponding c-aminoalcohols and final intramolecular cyclization of the latter by way of the intermediate tosylates, formed in situ. | - |
| dc.description | Fil: Kaufman, Teodoro Saul. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Instituto de Química Rosario; Argentina | - |
| dc.description | Fil: Amongero, Marcela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Instituto de Química Rosario; Argentina | - |
| dc.format | application/pdf | - |
| dc.format | application/pdf | - |
| dc.format | application/pdf | - |
| dc.format | application/pdf | - |
| dc.language | eng | - |
| dc.publisher | Elsevier | - |
| dc.relation | info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0040403913001482 | - |
| dc.relation | info:eu-repo/semantics/altIdentifier/doi/10.1016/j.tetlet.2013.01.090 | - |
| dc.relation | info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.tetlet.2013.01.090 | - |
| dc.rights | info:eu-repo/semantics/openAccess | - |
| dc.rights | https://creativecommons.org/licenses/by-nc-nd/2.5/ar/ | - |
| dc.source | reponame:CONICET Digital (CONICET) | - |
| dc.source | instname:Consejo Nacional de Investigaciones Científicas y Técnicas | - |
| dc.source | instacron:CONICET | - |
| dc.source.uri | http://hdl.handle.net/11336/15812 | - |
| dc.subject | Optically active azetidines | - |
| dc.subject | 1,2,3-Trisubstituted azetidines | - |
| dc.subject | Organocatalysis | - |
| dc.subject | Synthesis of nitrogen heterocycles | - |
| dc.subject | Química Orgánica | - |
| dc.subject | Ciencias Químicas | - |
| dc.subject | CIENCIAS NATURALES Y EXACTAS | - |
| dc.title | Synthesis of optically active 1,2,3-trisubstituted azetidines employing an organocatalytic approach with L-proline | - |
| dc.type | info:eu-repo/semantics/article | - |
| dc.type | info:eu-repo/semantics/publishedVersion | - |
| dc.type | info:ar-repo/semantics/articulo | - |
| Aparece en las colecciones: | CONICET | |
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