MARIA LUISA BENNASAR FELIX

University professor
Knowledge area: Química Orgànica

Grup de Síntesi d'Azapolicles Naturals (GSAN)

Contact Information
Department of Pharmacology, Toxicology and Medicinal Chemistry
Avda. Joan XXIII, s/n
934024540
bennasar(a)ub.edu

Academic training

Farmacia

Research interests

Metodologías de síntesis de compuestos nitrogenados. Reacciones radicalarias. Reacciones de metátesis de alquenos
Anulaciones en sustratos heterocíclicos. Radicales heterocíclicos y reacciones catalizadas por paladio

Projects

Nuevas estrategias en síntesis heterocíclica: radicales heterocíclicos y anulaciones catalizadas por paladio . 2010 - 2012 . Ref.CTQ2009-07175 . DIRECCIÓN GENERAL DE INVESTIGACIÓN. SUBDIRECCIÓN GENERAL DE PROYECTOS DE INVESTIGACIÓN . PI: Maria Luisa Bennasar Felix
Nuevas estrategias organometálicas para la formación de enlaces C-C en síntesis heterocíclica . 2013 - 2015 . Ref.CTQ2012-31391 . Ministerio de Economia y Competitividad . PI: Daniel Sole Arjo
Síntesis azaheterocíclica mediante metodologías organometálicas sostenibles . 2016 - 2018 . Ref.CTQ2015-64937-R . Ministerio de Economia y Competitividad . PI: Daniel Sole Arjo

Relevant publications

Bennasar, M.-L.; Zulaica, E.; Solé, D.; Roca, T.; García-Díaz, D.; Alonso, S. Total Synthesis of the Bridged Indole Alkaloid Apparicine. In Journal of Organic Chemistry. 2009 . https://doi.org/10.1021/jo901986v
Bennasar, M.L.; Solé, D.; Zulaica, E.; Alonso, S. A Straightforward synthetic entry to cleavamine-type indole alkaloids by a Ring-Closing Metathesis-vinyl halide Heck cyclization strategy. In Organic Letters. Volume 13. 2011
Solé, D.; Bennasar, M.-L.; Jiménez, I. Intramolecular palladium-catalysed enolate arylation of 2- and 3-iodoindole derivatives for the synthesis of beta-carbolines, gamma-carbolines, and pyrrolo[3,4-b]indoles. In Organic & Biomolecular Chemistry. Volume 9. 2011
Bennasar, M.L.; Roca, T. 3- Indolylacyl radical cyclizations upon pyridines and tetrahydropyridines: access to ergoline-related indole [cd]-fused isoquinolines. In Journal of Organic Chemistry. Volume 76. 2011 . https://doi.org/10.1021/jo2006279
Bennasar, M.L.; Zulaica, E.; Solé, D; Alonso, S. Sequential ring-closing metathesis-vinyl halide Heck cyclization reactions: access to the tetracyclic ring system of ervitsine. In Tetrahedron. Volume 68. 2012
Bennasar, M.L.; Solé, D.; Zulaica, E.; Alonso, S. Synthesis of cleavamine-type indole alkaloids and their 5-nor derivatives by a ring-closing metathesis-vinyl halide Heck cyclization strategy. In Tetrahedron. Volume 69. Number 12. 2013 . https://doi.org/10.1016/j.tet.2013.01.064
Bennasar, M.-L.; Solé, D.; Roca, T.; Valldosera, M. Exploratory studies toward a total synthesis of pericine (subincanadine E). In Tetrahedron. Volume 71. 2015 . https://doi.org/10.1016/j.tet.2015.02.074
Solé, D.; Bennasar, M.-L.; Roca, T.; Valldosera, M. Exploration of ring-closing enyne metathesis for the synthesis of azonino[5,4-b]indoles. In European Journal of Organic Chemistry. 2016 . https://doi.org/10.1002/ejoc.201501517
Solé, D.; Mariani, F.; Bennasar, M.-L.; Fernández, I. Palladium-catalyzed intramolecular carbene insertion into C(sp3)-H bonds. In Angewandte Chemie-International Edition. Volume 55. 2016 . https://doi.org/10.1002/anie.201602020
Bennasar, M.L. A Unified strategy for the synthesis of bridged indole alkaloids and their close analogues. In Targets in heterocyclic systems. Chemistry and properties. Volume. 17 . O. A. Attanasi, D. Spinelli, Società Chimica Italiana, Roma.. 2013