Synthesis of New Diversely Linked Biquinoline Derivatives by Multicomponent Imino-Diels–Alder Cycloaddition and Intramolecular Friedel–Crafts Cyclization
dc.contributor.author | Astudillo Saavedra, Luis | spa |
dc.contributor.author | Vallejos C., Gabriel | spa |
dc.contributor.author | Kouznetsov, Vladimir V. | spa |
dc.contributor.author | Gutierrez C., Margarita | spa |
dc.contributor.author | Meléndez Gómez, Carlos Mario | spa |
dc.contributor.author | Vargas Méndez, Leonor Y. | spa |
dc.contributor.author | Bermúdez Jaimes, John Hervin | spa |
dc.coverage.campus | CRAI-USTA Bogotá | spa |
dc.date.accessioned | 2020-01-22T18:08:14Z | spa |
dc.date.available | 2020-01-22T18:08:14Z | spa |
dc.date.issued | 2010 | spa |
dc.description | New and efficient routes for diversely linked 2,6¢-, 2,7¢-, 2,2¢-, or 2,8¢-biquinoline derivatives are reported. These routes are based on the powerful methodologies of imino-Diels–Alder cycloaddition reactions and intramolecular Friedel–Crafts cyclization reactions. | spa |
dc.description.domain | http://unidadinvestigacion.usta.edu.co | spa |
dc.format.mimetype | application/pdf | spa |
dc.identifier.doi | https://doi.org/10.1055/s-0029-1218613 | spa |
dc.identifier.uri | http://hdl.handle.net/11634/21049 | |
dc.relation.references | Jones, G. Pyridines and Their Benzo Derivatives: Synthesis, In Comprehensive Heterocyclic Chemistry, Vol. 2; Katritzky, A. R., Ed.; Pergamon Press: Oxford, 1984, 395 | spa |
dc.relation.references | Katritzky, A. R.; Rachwal, S.; Rachwal, B. Tetrahedron 1996, 52, 15031. | spa |
dc.relation.references | Kouznetsov, V.; Palma, A.; Ewert, C.; Varlamov, A. J. Heterocycl. Chem. 1998, 35, 761. | spa |
dc.relation.references | Kouznetsov, V. V.; Vargas Méndez, L. Y.; Meléndez Gómez, C. M. Curr. Org. Chem. 2005, 9, 141. | spa |
dc.relation.references | Glushenko, T. P.; Goncharov, V. I.; Aksenov, A. V. Chem. Heterocycl. Compd. 2008, 44, 973. | spa |
dc.relation.references | Broch, S.; Anizon, F.; Moreau, P. Synthesis 2008, 2039. | spa |
dc.relation.references | Chen, Y.-X.; Yang, L.-W.; Li, Y.-M.; Zhou, Z.-Y.; Lam, K.- H.; Chan, A. S. C.; Kwong, H.-L. Chirality 2000, 12, 510. | spa |
dc.relation.references | Ichikawa, J.; Mori, T.; Miyazaki, H.; Wada, Y. Synlett 2004, 1219. | spa |
dc.relation.references | Morsali, A.; Mahjoub, A. R.; Ramazani, A. J. Coord. Chem. 2004, 57, 347. | spa |
dc.relation.references | Trpkovska, M.; Šoptrajanov, B.; Pejov, L. J. Mol. Struct. 2003, 654, 21. | spa |
dc.relation.references | Youssef, A. O.; Khalil, M. M. H.; Ramadan, R. M.; Soliman, A. A. Transition Met. Chem. 2003, 28, 331. | spa |
dc.relation.references | Pazderski, L.; Tošuek, J.; Sitkowski, J.; Kozerski, L.; Szłyk, E. Magn. Reson. Chem. 2007, 45, 1059. | spa |
dc.relation.references | Guerrero, J.; Farías, L.; Lemus, L.; Quintanilla, A.; Mena, A.; Cortez, L.; Baggio, R. F.; Garland, M. T. Polyhedron 2006, 25, 9. | spa |
dc.relation.references | Kouznetsov, V. V. Tetrahedron 2009, 65, 2721. | spa |
dc.relation.references | Kouznetsov, V. V.; Mora Cruz, U. Lett. Org. Chem. 2006, 3, 699. | spa |
dc.relation.references | Kouznetsov, V. V.; Mora Cruz, U.; Zubkov, F. I.; Nikitina, E. V. Synthesis 2007, 375. | spa |
dc.relation.references | Kouznetsov, V. V.; Bohórquez Romero, A. R.; Astudillo Saavedra, L.; Fierro Medina, R. Mol. Diversity 2006, 10, 29. | spa |
dc.relation.references | Denmark, S. E.; Venkatraman, S. J. Org. Chem. 2006, 71, 1668. | spa |
dc.relation.references | Vargas, M. L. Y.; Castelli, M. V.; Kouznetsov, V. V.; Urbina, G. J. M.; López, S. N.; Sortino, M.; Enriz, R. D.;Ribas, J. C.; Zacchino, S. A. Bioorg. Med. Chem. 2003, 11, 1531. | spa |
dc.relation.references | Öcal, N.; Yolaçan, Ç.; Kaban, Ş.; Vargas Méndez, L. Y.; Kouznetsov, V. J. Heterocycl. Chem. 2001, 38, 233. | spa |
dc.rights | Atribución-NoComercial-CompartirIgual 2.5 Colombia | * |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-sa/2.5/co/ | * |
dc.subject.keyword | Biquinoline derivatives | spa |
dc.subject.keyword | Imino-Diels–Alder reactions | spa |
dc.subject.keyword | Cycloadditions | spa |
dc.subject.keyword | Intramolecular Friedel–Crafts reaction | spa |
dc.subject.keyword | Cyclizations | spa |
dc.title | Synthesis of New Diversely Linked Biquinoline Derivatives by Multicomponent Imino-Diels–Alder Cycloaddition and Intramolecular Friedel–Crafts Cyclization | spa |
dc.type.category | Generación de Nuevo Conocimiento: Artículos publicados en revistas especializadas - Electrónicos | spa |
Archivos
Bloque original
1 - 1 de 1
Cargando...
- Nombre:
- Synthesis of New Diversely Linked Biquinoline Derivatives by Multicomponen.pdf
- Tamaño:
- 155.6 KB
- Formato:
- Adobe Portable Document Format
- Descripción:
- Artículo SCOPUS
Bloque de licencias
1 - 1 de 1

- Nombre:
- license.txt
- Tamaño:
- 807 B
- Formato:
- Item-specific license agreed upon to submission
- Descripción: