Publications by authors named "Patrick Angibaud"

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Discovery and Pharmacological Characterization of JNJ-42756493 (Erdafitinib), a Functionally Selective Small-Molecule FGFR Family Inhibitor.
Timothy P S Perera, Eleonora Jovcheva, Laurence Mevellec, Jorge Vialard, Desiree De Lange, Patrick Angibaud

Mol Cancer Ther· June 2017

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Iron-Catalyzed Synthesis of Sulfur-Containing Heterocycles.
Cyril Bosset, Gauthier Lefebvre, Patrick Angibaud, Ian Stansfield, Lieven Meerpoel

J Org Chem· April 2017

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Access to Silylated Pyrazole Derivatives by Palladium-Catalyzed C-H Activation of a TMS group.
Laetitia Mistico, Olivier Querolle, Lieven Meerpoel, Patrick Angibaud, Muriel Durandetti

Chemistry· July 2016

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Tankyrase inhibition impairs directional migration and invasion of lung cancer cells by affecting microtubule dynamics and polarity signals.
Barbara Lupo, Jorge Vialard, Francesco Sassi, Patrick Angibaud, Alberto Puliafito

BMC Biol· January 2016

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Iron-Catalyzed Synthesis of C2 Aryl- and N-Heteroaryl-Substituted Tetrahydropyrans.
Cyril Bosset, Patrick Angibaud, Ian Stanfield, Lieven Meerpoel, Didier Berthelot

J Org Chem· December 2015

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Anionic access to silylated and germylated binuclear heterocycles.
Thomas Boddaert, Cyril François, Laetitia Mistico, Olivier Querolle, Lieven Meerpoel, Patrick Angibaud

Chemistry· August 2014

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Synthesis of substituted indenones and indanones by a Suzuki-Miyaura coupling/acid-promoted cyclisation sequence.
Alexey N Butkevich, Beatrice Ranieri, Lieven Meerpoel, Ian Stansfield, Patrick Angibaud

Org Biomol Chem· February 2014

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Cobalt-catalyzed diastereoselective synthesis of C-furanosides. Total synthesis of (-)-isoaltholactone.
Lionel Nicolas, Eva Izquierdo, Patrick Angibaud, Ian Stansfield, Lieven Meerpoel

J Org Chem· December 2013

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Tandem Suzuki-Miyaura coupling/acid-catalyzed cyclization between vinyl ether boronates and vinyl halides: a concise approach to polysubstituted furans.
Alexey N Butkevich, Lieven Meerpoel, Ian Stansfield, Patrick Angibaud, Andrei Corbu

Org Lett· August 2013

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Two-step one-pot synthesis of benzoannulated spiroacetals by Suzuki-Miyaura coupling/acid-catalyzed spiroacetalization.
Alexey N Butkevich, Andrei Corbu, Lieven Meerpoel, Ian Stansfield, Patrick Angibaud

Org Lett· October 2012

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Diastereoselective metal-catalyzed synthesis of C-aryl and C-vinyl glycosides.
Lionel Nicolas, Patrick Angibaud, Ian Stansfield, Pascal Bonnet, Lieven Meerpoel

Angew Chem Int Ed Engl· October 2012

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Intramolecular sila-Matteson rearrangement: a general access to silylated heterocycles.
Cyril François, Thomas Boddaert, Muriel Durandetti, Olivier Querolle, Luc Van Hijfte, Patrick Angibaud

Org Lett· April 2012

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Potent, selective inhibitors of fibroblast growth factor receptor define fibroblast growth factor dependence in preclinical cancer models.
Matthew Squires, George Ward, Gordan Saxty, Valerio Berdini, Anne Cleasby, Patrick Angibaud

Mol Cancer Ther· September 2011

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Identification of a series of substituted 2-piperazinyl-5-pyrimidylhydroxamic acids as potent histone deacetylase inhibitors.
Patrick Angibaud, Kristof Van Emelen, Laurence Decrane, Sven van Brandt, Peter Ten Holte

Bioorg Med Chem Lett· January 2010

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JNJ-26481585, a novel "second-generation" oral histone deacetylase inhibitor, shows broad-spectrum preclinical antitumoral activity.
Janine Arts, Peter King, Ann Mariën, Wim Floren, Ann Beliën, Patrick Angibaud

Clin Cancer Res· November 2009

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Impact on farnesyltransferase inhibition of 4-chlorophenyl moiety replacement in the Zarnestra series.
Patrick Angibaud, Laurence Mevellec, Christophe Meyer, Xavier Bourdrez, Patricia Lezouret

Eur J Med Chem· May 2007

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Discovery of pyrimidyl-5-hydroxamic acids as new potent histone deacetylase inhibitors.
Patrick Angibaud, Janine Arts, Kristof Van Emelen, Virginie Poncelet, Isabelle Pilatte

Eur J Med Chem· June 2005

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4-methyl-1,2,4-triazol-3-yl heterocycle as an alternative to the 1-methylimidazol-5-yl moiety in the farnesyltransferase inhibitor ZARNESTRA.
Patrick Angibaud, Ashis K Saha, Xavier Bourdrez, David W End, Eddy Freyne

Bioorg Med Chem Lett· December 2003

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Substituted azoloquinolines and -quinazolines as new potent farnesyl protein transferase inhibitors.
Patrick Angibaud, Xavier Bourdrez, David W End, Eddy Freyne, Michel Janicot

Bioorg Med Chem Lett· December 2003

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Farnesyl protein transferase inhibitor ZARNESTRA R115777 - history of a discovery.
Marc Venet, David End, Patrick Angibaud

Curr Top Med Chem· June 2003

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5-imidazolyl-quinolinones, -quinazolinones and -benzo-azepinones as farnesyltransferase inhibitors.
Patrick Angibaud, Xavier Bourdrez, Ann Devine, David W End, Eddy Freyne

Bioorg Med Chem Lett· May 2003

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