Chiral gold(I) vs chiral silver complexes as catalysts for the enantioselective synthesis of the second generation GSK-hepatitis C virus inhibitor
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http://hdl.handle.net/10045/18175
| Títol: | Chiral gold(I) vs chiral silver complexes as catalysts for the enantioselective synthesis of the second generation GSK-hepatitis C virus inhibitor |
|---|---|
| Autors: | Martín Rodríguez, María | Nájera, Carmen | Sansano, Jose M. | Cózar Ruano, Abel de | Cossío Mora, Fernando Pedro |
| Grups d'investigació o GITE: | Procesos Catalíticos en Síntesis Orgánica |
| Centre, Departament o Servei: | Universidad de Alicante. Departamento de Química Orgánica | Universidad del País Vasco. Departamento de Química Orgánica |
| Paraules clau: | BINAP | 1,3-dipolar cycloaddition | Gold | HCV | Phosphoramidite | Silver | Viral inhibitor |
| Àrees de coneixement: | Química Orgánica |
| Data de creació: | 2011 |
| Data de publicació: | 19-de juliol-2011 |
| Editor: | Beilstein-Institut |
| Citació bibliogràfica: | MARTÍN RODRÍGUEZ, María, et al. “Chiral gold(I) vs chiral silver complexes as catalysts for the enantioselective synthesis of the second generation GSK-hepatitis C virus inhibitor”. Beilstein Journal of Organic Chemistry. No. 7 (2011). ISSN 1860-5397, pp. 988-996 |
| Resum: | The synthesis of a GSK 2nd generation inhibitor of the hepatitis C virus, by enantioselective 1,3-dipolar cycloaddition between a leucine derived iminoester and tert-butyl acrylate, was studied. The comparison between silver(I) and gold(I) catalysts in this reaction was established by working with chiral phosphoramidites or with chiral BINAP. The best reaction conditions were used for the total synthesis of the hepatitis C virus inhibitor by a four step procedure affording this product in 99% ee and in 63% overall yield. The origin of the enantioselectivity of the chiral gold(I) catalyst was justified according to DFT calculations, the stabilizing coulombic interaction between the nitrogen atom of the thiazole moiety and one of the gold atoms being crucial. |
| Patrocinadors: | This work has been supported by the DGES of the Spanish Ministerio de Ciencia e Innovación (MICINN) (Consolider INGENIO 2010 CSD2007-00006, FEDER-CTQ2007-62771/BQU, CTQ2007/67528, CTQ2010-20387 and by the Hispano-Brazilian project PHB2008-0037-PC), Generalitat Valenciana (PROMETEO/ 2009/039), the Basque government (Grant IT-324-07) and by the University of Alicante. M. M.-R. Also thanks DGES for a grant. |
| URI: | http://hdl.handle.net/10045/18175 |
| ISSN: | 1860-5397 |
| DOI: | 10.3762/bjoc.7.111 |
| Idioma: | eng |
| Tipus: | info:eu-repo/semantics/article |
| Drets: | © 2011 Martín-Rodríguez et al; licensee Beilstein-Institut. This is an Open Access article under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (http://www.beilstein-journals.org/bjoc). |
| Revisió científica: | si |
| Versió de l'editor: | http://dx.doi.org/10.3762/bjoc.7.111 |
| Apareix a la col·lecció: | INV - PCSO - Artículos de Revistas INV - SINTAS - Artículos de Revistas |
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