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Bernat Vidal

Biomimetic Total Synthesis of Ervitsine and Indole Alkaloids of the Ervatamine Group via 1,4-Dihydropyridines
1997 · M.-Lluïsa Bennasar, Bernat Vidal, et al. · The Journal of Organic Chemistry · 87
Novel Chiral Bidentateη5-Cyclopentadienylphosphine Ligands: Their Asymmetric Induction at the Ruthenium(II) Center and Application in Catalysis
1999 · Barry M. Trost, Bernat Vidal, et al. · Chemistry - A European Journal · 71
Nucleophilic Addition of 1-Acetylindole Enolates to Pyridinium Salts. Stereoselective Formal Synthesis of (±)-Geissoschizine and (±)-Akagerine via 1,4-Dihydropyridines
1999 · M.-Lluïsa Bennasar, Juan-Miguel Jiménez, et al. · The Journal of Organic Chemistry · 45
Design, Synthesis, and Structure−Activity Relationships of 1-,3-,8-, and 9-Substituted-9-deazaxanthines at the Human A2BAdenosine Receptor
2005 · Angelo Carotti, Maria Isabel Cadavid, et al. · Journal of Medicinal Chemistry · 38
Prediction of the skin permeability of topical drugs using in silico and in vitro models
2019 · Cristina Alonso, Víctor Carrer, et al. · European Journal of Pharmaceutical Sciences · 37
First total synthesis of the indole alkaloid ervitsine. A straightforward, biomimetic approach
1993 · M. Lluisa Bennasar, Bernat Vidal, et al. · Journal of the American Chemical Society · 37
1,7-Naphthyridine 1-Oxides as Novel Potent and Selective Inhibitors of p38 Mitogen Activated Protein Kinase
2011 · Wenceslao Lumeras, Laura Vidal, et al. · Journal of Medicinal Chemistry · 35
Design, Synthesis, and Structure−Activity Relationships of AminopyridineN-Oxides, a Novel Scaffold for the Potent and Selective Inhibition of p38 Mitogen Activated Protein Kinase
2009 · Wenceslao Lumeras, Francisco Caturla, et al. · Journal of Medicinal Chemistry · 33
Discovery and Characterization of 4‘-(2-Furyl)-N-pyridin-3-yl-4,5‘-bipyrimidin-2‘-amine (LAS38096), a Potent, Selective, and Efficacious A2BAdenosine Receptor Antagonist
2007 · Bernat Vidal, Arsenio Nueda, et al. · Journal of Medicinal Chemistry · 33
Novel triazolopyridylbenzamides as potent and selective p38α inhibitors
2012 · Josep Aiguadé, Cristina Balagué, et al. · Bioorganic & Medicinal Chemistry Letters · 32
Indolin-2-one p38α inhibitors I: Design, profiling and crystallographic binding mode
2011 · Paul Eastwood, Jacob González, et al. · Bioorganic & Medicinal Chemistry Letters · 30
A novel inhaled Syk inhibitor blocks mast cell degranulation and early asthmatic response
2015 · Isabel Ramis, Raquel Otal, et al. · Pharmacological Research · 29
Formal stereoselective synthesis of (±)-akagerine
1998 · M.-Lluïsa Bennasar, Bernat Vidal, et al. · Chemical Communications · 26
A synthetic route to the alkaloids of the ervatamine group. First total synthesis of (±)-6-oxo-16-episilicine
1996 · M.-Lluïsa Bennasar, Bernat Vidal, et al. · Chemical Communications · 26
A short route for the construction of the tetracyclic ring system of silicine-methuenine alkaloids
1996 · M.-Lluïsa Bennasar, Bernat Vidal, et al. · Tetrahedron Letters · 24
Total Synthesis of Indole Alkaloids of the Ervatamine Group. A Biomimetic Approach
1996 · M.-Lluïsa Bennasar, Bernat Vidal, et al. · The Journal of Organic Chemistry · 24
Discovery of 7-azaindole derivatives as potent Orai inhibitors showing efficacy in a preclinical model of asthma
2015 · Cristina Esteve, Jacob González, et al. · Bioorganic & Medicinal Chemistry Letters · 23
New pyrrolopyrimidin-6-yl benzenesulfonamides: Potent A2B adenosine receptor antagonists
2006 · Cristina Esteve, Arsenio Nueda, et al. · Bioorganic & Medicinal Chemistry Letters · 23
Solid-phase synthesis of sulfamides
2002 · Cristina Esteve, Bernat Vidal · Tetrahedron Letters · 23
Discovery of potent and selective bicyclic A2B adenosine receptor antagonists via bioisosteric amide replacement
2010 · Paul Eastwood, Jacob Gonzalez, et al. · Bioorganic & Medicinal Chemistry Letters · 21
Structure-activity relationships (SAR) and structure-kinetic relationships (SKR) of sulphone-based CRTh2 antagonists
2016 · Maria Antonia Buil, Marta Calbet, et al. · European Journal of Medicinal Chemistry · 20
Highly potent aminopyridines as Syk kinase inhibitors
2012 · Marcos Castillo, Pilar Forns, et al. · Bioorganic & Medicinal Chemistry Letters · 20
Discovery of N-(5,6-diarylpyridin-2-yl)amide derivatives as potent and selective A2B adenosine receptor antagonists
2010 · Paul Eastwood, Jacob Gonzalez, et al. · Bioorganic & Medicinal Chemistry Letters · 20
Discovery of LAS101057: A Potent, Selective, and Orally Efficacious A2B Adenosine Receptor Antagonist
2010 · Paul Eastwood, Cristina Esteve, et al. · ACS Medicinal Chemistry Letters · 19
Nucleophilic Addition of 2-Acetylindole Enolates to Pyridinium Salts. Acylation of the Intermediate Dihydropyridines
1995 · M.-Lluiesa Bennasar, Bernat Vidal, et al. · The Journal of Organic Chemistry · 19
Works count: 53
Citation count: 941
H-index: 20
I10-index: 33
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