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Lluís Pagès
Observed names:
L. PAGES,
L.L. Pagès,
Lluis Pages,
Lluis Pagès,
Lluís Pagès,
Lluı́s Pagès
show all 6
Institution:
Almirall (Spain)
Observed institutions:
Consejo Superior de Investigaciones Científicas,
Centro de Investigación y Desarrollo,
Almirall (Spain),
Universitat de Barcelona
ORCID:
0000-0002-3367-9529
Observed ORCID:
0000-0002-3367-9529
OpenAlex ID:
A5031152143
PDE4 inhibitors: a review of current developments (2005 – 2009)
2009
·
Lluís Pagès
, Amadeu Gavaldà
, et al.
·
Expert Opinion on Therapeutic Patents
·
103
Ring-fused and spiro cyclopentenones by Ni(CO)4-promoted intermolecular carbonylative cycloaddition of acetylenes with 3-halo- and 1-(halomethyl)cycloalkenes
1992
·
Lluis Pages
, Amadeu Llebaria
, et al.
·
Journal of the American Chemical Society
·
58
Design, Synthesis, and Biological Activities of New Thieno[3,2-d]pyrimidines as Selective Type 4 Phosphodiesterase Inhibitors
1998
·
María I. Crespo
, Lluís Pagès
, et al.
·
Journal of Medicinal Chemistry
·
47
Discovery of a Novel Inhaled PI3Kδ Inhibitor for the Treatment of Respiratory Diseases
2018
·
Montse Erra
, Joan Taltavull
, et al.
·
Journal of Medicinal Chemistry
·
39
Synthesis and Biological Activity of Pyrido[3′,2′:4,5]thieno[3,2-d]pyrimidines as Phosphodiesterase Type 4 Inhibitors
2010
·
Joan Taltavull
, Jordi Serrat
, et al.
·
Journal of Medicinal Chemistry
·
33
Biphenyl Pyridazinone Derivatives as Inhaled PDE4 Inhibitors: Structural Biology and Structure–Activity Relationships
2016
·
Jordi Gràcia
, Maria Antonia Buil
, et al.
·
Journal of Medicinal Chemistry
·
29
Synthesis and Structure−Activity Relationships of Novel Histamine H 1 Antagonists: Indolylpiperidinyl Benzoic Acid Derivatives
2004
·
Silvia Fonquerna
, Montse Miralpeix
, et al.
·
Journal of Medicinal Chemistry
·
25
Influence of functional substitution of allyl halides on their ni(co)4 promoted carbonylative cycloaddition with acetylenes
1992
·
Francisco Camps
, Josep M. Moreto
, et al.
·
Tetrahedron
·
24
Synthetic applications of 2-aryl-4-piperidones. X Synthesis of 3-aminopiperidines, potential substance P antagonists
1995
·
Anna Diez
, Aline Voldoire
, et al.
·
Tetrahedron
·
21
Synthesis and biological activity of pyrido[3′,2′:4,5]furo[3,2-d]pyrimidine derivatives as novel and potent phosphodiesterase type 4 inhibitors
2011
·
Joan Taltavull
, Jordi Serrat
, et al.
·
European Journal of Medicinal Chemistry
·
19
Synthesis and structure–activity relationships of γ-carboline derivatives as potent and selective cysLT1 antagonists
2009
·
Josep Bonjoch
, Faïza Diaba
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
19
Fused bicyclic systems through a ni-mediated intermolecular cyclopentenone annulation
1992
·
Francisco Camps
, Amadeu Llebaria
, et al.
·
Tetrahedron Letters
·
17
Synthesis and structure–activity relationships of piperidinylpyrrolopyridine derivatives as potent and selective H1 antagonists
2005
·
Silvia Fonquerna
, Montse Miralpeix
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
16
New practical synthesis of spirocyclopentenones
1992
·
Francisco Camps
, Amadeu Llebaria
, et al.
·
Tetrahedron Letters
·
14
N,N′‐Cyclization of carbodiimides with 2‐(bromomethyl)acrylic acid. A direct entry to the system 5‐methylene‐6H‐pyrimidine‐2,4‐dione, a new class of thymine analogues
1996
·
J. M. Anglada
, T. Campos
, et al.
·
Journal of Heterocyclic Chemistry
·
12
Preference for β-H elimination in the termination of the Ni-promoted carbonylative cycloaddition of 2-haloethylidene-cycloalkanes and alkynes
1998
·
Fabiola Vilaseca
, Lluı́s Pagès
, et al.
·
Journal of Organometallic Chemistry
·
7
Discovery of Potent PDE4 Inhibitors with 3(2H)-Pyridazinone Scaffold: Synthesis, In Silico Studies and In Vitro/Vivo Evaluation
2026
·
Claudia Vergelli
, Letizia Crocetti
, et al.
·
Molecules
·
1
PDF
Discovery of LAS194046: A Potent and Selective pan-Janus Kinase (JAK) Inhibitor with a Suitable Profile for Inhaled Administration
2026
·
Jordi Bach
, Daniel Pérez
, et al.
·
Journal of Medicinal Chemistry
ChemInform Abstract: Synthesis and Biological Activity of Pyrido[3′,2′:4,5]furo[3,2‐d]pyrimidine Derivatives as Novel and Potent Phosphodiesterase Type 4 Inhibitors.
2012
·
Lluis Pages
, et al. et al.
·
ChemInform
ChemInform Abstract: Preference for β‐H Elimination in the Termination of the Ni‐Promoted Carbonylative Cycloaddition of 2‐Haloethylidene‐cycloalkanes and Alkynes.
1998
·
F. VILASECA
, L. PAGES
, et al.
·
ChemInform
ChemInform Abstract: Synthetic Applications of 2‐Aryl‐4‐piperidones. Part 10. Synthesis of 3‐Aminopiperidines, Potential Substance P Antagonists.
1995
·
A. DIEZ
, A. VOLDOIRE
, et al.
·
ChemInform
ChemInform Abstract: Ring‐Fused and Spiro Cyclopentenones by Ni(CO)4‐Promoted Intermolecular Carbonylative Cycloaddition of Acetylenes with 3‐Halo‐ and 1‐(Halomethyl)cycloalkenes.
1993
·
L. PAGES
, A. LLEBARIA
, et al.
·
ChemInform
ChemInform Abstract: Influence of Functional Substitution of Allyl Halides on Their Ni(CO)4‐ Promoted Carbonylative Cycloaddition with Acetylenes.
1992
·
F. CAMPS
, J. M. MORETO
, et al.
·
ChemInform
ChemInform Abstract: New Practical Synthesis of Spirocyclopentenones.
1992
·
F. CAMPS
, A. LLEBARIA
, et al.
·
ChemInform
ChemInform Abstract: Fused Bicyclic Systems Through a Ni‐Mediated Intermolecular Cyclopentenone Annulation.
1992
·
F. CAMPS
, A. LLEBARIA
, et al.
·
ChemInform
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Works count:
25
Citation count:
484
H-index:
14
I10-index:
15
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