V. Collot

发表

Suzuki-type cross-coupling reaction of 3-iodoindazoles with aryl boronic acids: A general and flexible route to 3-arylindazoles

S. Rault, P. Dallemagne, P. Bovy, 1999 .

Heck cross-coupling reaction of 3-iodoindazoles with methyl acrylate: a mild and flexible strategy to design 2-aza tryptamines

S. Rault, V. Collot, Didier Varlet, 2000 .

7-Methoxy-1H-indazole, a new inhibitor of neuronal nitric oxide synthase.

S. Rault, J. Sopková-de Oliveira Santos, V. Collot, 2002, Acta crystallographica. Section C, Crystal structure communications.

Radiotracers for the Central Serotoninergic System

T. Cailly, V. Collot, Reynald Mangeant, 2022, Pharmaceuticals.

7-Nitro-1H-indazole, an inhibitor of nitric oxide synthase.

S. Rault, J. Sopková-de Oliveira Santos, V. Collot, 2000, Acta crystallographica. Section C, Crystal structure communications.

Thiofunctionalization of Electron‐Rich Heteroarenes through Magnesiation and Trapping with Octasulfur

T. Cailly, F. Fabis, V. Collot, 2021, Advanced Synthesis & Catalysis.

A new and efficient synthesis of 2-azatryptophans

S. Rault, V. Collot, S. Stiebing, 2006 .

Sonogashira cross-coupling reaction of 3-iodoindazoles with various terminal alkynes: a mild and flexible strategy to design 2-aza tryptamines

S. Rault, C. Alayrac, B. Witulski, 2002 .

Inhibition of neuronal nitric oxide synthase by 7-methoxyindazole and related substituted indazoles.

E. Mackenzie, S. Rault, F. Dauphin, 2001, Bioorganic & medicinal chemistry letters.

Iodoindazoles with Selective Magnesiation at Position 3: A Route to Highly Functionalized Indazoles.

T. Cailly, F. Fabis, C. Fossey, 2016, Chemistry.

Analogs of NPFF, a neuropeptide which modulates morphine analgesia

J. Bourguignon, G. Simonnet, J. Laulin, 1997 .

Design and synthesis of a new indazole library: direct conversion of N-methoxy-N-methylamides (Weinreb amides) to 3-keto and 3-formylindazoles

S. Rault, Rémi Legay, V. Collot, 2007 .

Synthesis of novel halopyridinylboronic acids and esters. Part 2: 2,4, or 5-Halopyridin-3-yl-boronic acids and esters

S. Rault, A. Bouillon, J. Lancelot, 2002 .

Regiospecific thermal C-acylation of imidazo [1,2-a] pyridines via an N-acylimidazolium intermediate

J. Bourguignon, S. Chayer, M. Schmitt, 1998 .

First combined selective N- and C-arylations with boronic acids: application to the synthesis of 1,3-diarylindazoles

S. Rault, P. Bovy, V. Collot, 2000 .

Synthesis and biological evaluation of five-membered heterocycles fused to cyclopenta[c]thiophene as new antitumor agents.

S. Rault, R. Bureau, P. Dallemagne, 2003, Bioorganic & medicinal chemistry.

A general synthesis of diversely substituted indazoles and hetero-aromatic derivatives from o-halo-(het)arylaldehydes or -phenones

T. Cailly, F. Fabis, V. Collot, 2014 .

4-substituted indazoles as new inhibitors of neuronal nitric oxide synthase.

S. Rault, M. Boulouard, P. Schumann-Bard, 2007, Bioorganic & medicinal chemistry letters.

Inhibitory effects and spectral interactions of isomeric methoxyindazoles on recombinant nitric oxide synthases.

J. Boucher, S. Rault, P. Schumann-Bard, 2003, Nitric oxide : biology and chemistry.

A two-steps benzotriazole-assisted synthesis of 3-amino-2-ethoxycarbonyl imidazo [1,2-a] pyridines and related compounds

J. Bourguignon, M. Schmitt, V. Collot, 1996 .

Efficient and simple synthesis of 3-aryl-1H-pyrazoles

S. Rault, A. Bouillon, C. Mahatsekake, 2006 .

Synthesis of novel halopyridinylboronic acids and esters. Part 4: Halopyridin-2-yl-boronic acids and esters are stable, crystalline partners for classical Suzuki cross-coupling☆

Jana Sopkova-de Oliveira Santos, S. Rault, A. Bouillon, 2003 .

A NOVEL METHOD OF PREPARATION OF 3-ACYLIMIDAZO1,2-ALPHA PYRIDINES

J. Bourguignon, M. Schmitt, V. Collot, 1997 .

Sequential Sonogashira and Suzuki Cross-Coupling Reactions in the Indole and Indazole Series

S. Rault, C. Alayrac, B. Witulski, 2005 .

New practical access to 2-azatryptophans and dehydro derivatives via the Wittig-Horner reaction

Jana Sopkova-de Oliveira Santos, S. Rault, J. Lohier, 2007 .

First Combined Selective N- and C-Arylations with Boronic Acids: Application to the Synthesis of 1,3-Diarylindazoles.

S. Rault, P. Bovy, V. Collot, 2001 .

Synthesis, Pharmacological Study and Modeling of 7-Methoxyindazole and Related Substituted Indazoles as Neuronal Nitric Oxide Synthase Inhibitors

Sylvain Rault, Nathalie Colloc'h, Pascale Schumann-Bard, 2003, Journal of enzyme inhibition and medicinal chemistry.

Synthesis of new dehydro 2-azatryptophans and derivatives via heck cross-coupling reactions of 3- iodoindazoles with methyl 2-(acetylamino)acrylate

S. Rault, V. Collot, S. Stiebing, 2006 .

Regiospecific Functionalization of Indole-2-carboxylates and Diastereoselective Preparation of the Corresponding Indolines

J. Bourguignon, M. Schmitt, P. Marwah, 1999 .

Synthesis of novel triazolopyridylboronic acids and esters. Study of potential application to Suzuki-type reactions

S. Rault, A. Bouillon, J. Lancelot, 2004 .

Regiospecific Functionalization of Indole‐2‐carboxylates and Diastereoselective Preparation of the Corresponding Indolines.

J. Bourguignon, M. Schmitt, P. Marwah, 2000 .

Reactivity of 3-iodoimidazo[1,2-a]pyridines using a Suzuki-type cross-coupling reaction.

S. Rault, A. Gueiffier, V. Collot, 2000, The Journal of organic chemistry.

Suzuki-Type Cross-Coupling Reaction of 3-Iodoindazoles with Aryl Boronic Acids: A General and Flexible Route to 3-Arylindazoles.

S. Rault, P. Dallemagne, P. Bovy, 2010 .

Reactivity of 3‐Iodoimidazo[1,2‐a]pyridines Using a Suzuki‐Type Cross‐Coupling Reaction.

S. Rault, A. Gueiffier, V. Collot, 2001 .

An efficient two-step total synthesis of the quaterpyridine nemertelline.

S. Rault, A. Voisin, A. Bouillon, 2003, The Journal of organic chemistry.

Synthesis of 3-Phenylindoline-2-carboxamides as Semi-Rigid Phenylalanine Mimetics

J. Bourguignon, B. Norberg, M. Schmitt, 1997 .

A General Synthesis of Diversely Substituted Indazoles and Hetero-Aromatic Derivatives from O-Halo-(het)arylaldehydes or -phenones.

T. Cailly, F. Fabis, V. Collot, 2015 .

New hypotheses for the binding mode of 4- and 7-substituted indazoles in the active site of neuronal nitric oxide synthase.

S. Rault, M. Boulouard, P. Schumann-Bard, 2012, Bioorganic & medicinal chemistry.

Protected Indazole Boronic Acid Pinacolyl Esters: Facile Syntheses and Studies of Reactivities in Suzuki—Miyaura Cross‐Coupling and Hydroxydeboronation Reactions.

S. Rault, Elodie Lohou, V. Collot, 2009 .

Protected Indazole Boronic Acid Pinacolyl Esters: Facile Syntheses and Studies of Reactivities in Suzuki-Miyaura Cross-Coupling and Hydroxydeboronation Reactions

S. Rault, Elodie Lohou, V. Collot, 2009 .

Synthesis and biological evaluation of cyclopenta[c]thiophene related compounds as new antitumor agents.

S. Rault, O. Renault, R. Bureau, 2002, Bioorganic & medicinal chemistry.

YC-1, an activation inductor of soluble guanylyl cyclase.

S. Rault, J. Sopková-de Oliveira Santos, V. Collot, 2000, Acta crystallographica. Section C, Crystal structure communications.

A facile synthetic route to new pyrazoloisoindolones

S. Rault, C. Mahatsekake, Anne-Laure Gérard, 2007 .

Direct Access to 3-Aminoindazolesby Buchwald-Hartwig C-N Coupling Reaction

S. Rault, Elodie Lohou, V. Collot, 2011 .

ChemInform Abstract: Synthesis of Novel Halopyridinylboronic Acids and Esters. Part 2. 2,4, or 5-Halopyridin-3-yl-boronic Acids and Esters.

S. Rault, A. Bouillon, J. Lancelot, 2002 .