Accueil › Annuaire des chercheurs › Henri Doucet
Henri Doucet
Affiliation : Centre National de la Recherche Scientifique · Institut des Sciences Chimiques de Rennes · Université de Rennes
- 103Publications (affiliation française)
- 644Publications au total
- 14254Citations
- 63Indice h
Profil de recherche
Henri Doucet compte 103 publications référencées (2007–2026). Ses travaux paraissent principalement dans « ChemInform », « Tetrahedron » et « Tetrahedron Letters ». Son article le plus cité, « Direct arylation of oxazole and benzoxazole with aryl or heteroaryl halides using a palladium–diphosphine catalyst » (2007), a été cité 96 fois. 8 de ces publications datent des trois dernières années d’activité. Ses travaux sont cosignés avec au moins 12 chercheurs, notamment dans des établissements de Tunisie, Algérie, Maroc.
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Créer mon profil gratuit Ajouter mes publicationsDomaines de recherche
- Catalytic Cross-Coupling Reactions
- Catalytic C–H Functionalization Methods
- Sulfur-Based Synthesis Techniques
- Catalytic Alkyne Reactions
- Crystal structures of chemical compounds
Publications (103)
- Reactivity of bromobenzenes bearing an unprotected hydroxyalkyl substituent in palladium-catalyzed C–H bond heteroarylation
- Palladium-catalyzed selective C5 H bond arylation of pyrazole using hydroxymethyl substituent as blocking group
- Evaluation of C3-substituents on pyrazoles as remote directing groups in palladium-catalyzed direct arylation
- Hydroxymethyl as Directing Group for the Regioselective Palladium-Catalyzed C–H Bond C2-Arylation of a C3-Substituted Furan
- Synthesis of C5-arylated pyrazoles from a pyrazole-4-carboxylate by a palladium-catalyzed C5–H bond activation/C4-decarboxylation sequence
- Influence of Benzothiophene C2 ‐Substituents in Palladium‐Catalyzed Direct C3 ‐Arylation
- Mono or double Pd-catalyzed C–H bond functionalization for the annulative π-extension of 1,8-dibromonaphthalene: a one pot access to fluoranthene derivatives
- Palladium‐Catalyzed C4,C5‐Diarylation of Isoxazole‐3‐Carboxylate by Double C−H Bond Functionalization
- Palladium-catalyzed direct C5-arylation or C4,C5-diarylation of 2-alkylisothiazol-3-ones
- Anti-Corrosive Properties and Quantum Chemical Studies of (Benzoxazol) Derivatives on Mild Steel in HCl (1 M)
- Anti-Corrosive Properties and Quantum Chemical Studies of (Benzoxazol) Derivatives on Mild Steel in HCl (1 M)
- Exploiting the Reactivity of Fluorinated 2‑Arylpyridines in Pd-Catalyzed C–H Bond Arylation for the Preparation of Bright Emitting Iridium(III) Complexes
- Regiodivergent Late‐Stage Pd‐ or Ru‐Catalyzed C–H Bond Functionalization Applied to the Straightforward Synthesis of N ‐Methylated Diflufenican Derivatives
- Palladium−Ruthenium Catalyst Complementarity Strengthens Ortho‐Directed C−H Bond Arylation of 2‐Arylpyrazines
- Identification of novel antifungal agents: antimicrobial evaluation, SAR, ADME–Tox and molecular docking studies of a series of imidazole derivatives
- Late-Stage Diversification of Imidazole-Based Pharmaceuticals through Pd-Catalyzed Regioselective C–H Bond Arylations
- Intermolecular Followed by Intramolecular Palladium‐Catalyzed Direct Arylation for the Synthesis of π‐Extended Aromatic Compounds Containing One or Two Heteroelements
- A Straightforward One‐Step Access to Ticlopidine Derivatives Arylated at the C5‐Position of the Thienyl Ring via Pd‐Catalyzed Direct Arylations
- Studies of Catecholase Activities of N-donor Bidentates Ligands derivated from Benzoxazole with Copper (II) Salts
- Late stage Pd-catalyzed C-H bond functionalization: A powerful tool for the one step access to arylated Cyproheptadine and cyclobenzaprine derivatives
- Reactivity of N-methyl-N-(polyfluorobenzyl)acetamides and N-methyl-N-(polyfluorobenzyl)benzamides in Pd-catalyzed C–H bond arylation
- In vitro screening, homology modeling and molecular docking studies of some pyrazole and imidazole derivatives
- Catalyst-Controlled Regiodivergent C–H Arylation Site of Fluorinated 2-Arylpyridine Derivatives: Application to Luminescent Iridium(III) Complexes
- Novel cyclometallated 5-π-delocalized donor-1,3-di(2-pyridyl)benzene platinum( ii ) complexes with good second-order nonlinear optical properties
- Reactivity of 5-aminopyrazoles bearing a cyclopropyl group at C3-position in palladium-catalyzed direct C4-arylation
- Synthesis of C9,C10‐Diheteroarylated Phenanthrenes via Palladium‐Catalyzed C–H Bond Activation
- Access to (Hetero)arylated Selenophenes via Palladium‐catalysed Stille, Negishi or Suzuki Couplings or C−H Bond Functionalization Reaction
- Unprecedented Access to β‐Arylated Selenophenes through Palladium‐Catalysed Direct Arylation
- Palladium-Catalyzed C–H Bond Functionalization of 6,6-Diphenylfulvenes: An Easier Access to C1-Arylated and C1,C4-Diarylated Fulvenes
- Palladium-catalyzed regioselective C–H bond arylations at the C3 position of ortho-substituted fluorobenzenes
- Palladium‐Catalyzed Regioselective Direct Arylation of Benzofurazans at the C‐4 Position
- Reactivity of benzofuran and benzothiophene in palladium-catalysed direct C2,C3-diarylations
- Synthesis of 2-(fluorinated aryl)pyridine derivatives via palladium-catalyzed C H bond arylation of fluorobenzenes using 2-halopyridines as aryl sources
- Reactivity of bromoselenophenes in palladium-catalyzed direct arylations
- Palladium-Catalyzed Regioselective C–H Bond Arylations of Benzoxazoles and Benzothiazoles at the C7 Position
- Reactivity of 2,1‐Benzisoxazole in Palladium‐Catalyzed Direct Arylation with Aryl Bromides
- Direct C3‐Arylation of 2 H‐Indazole Derivatives with Aryl Bromides by using Low Loading of a Phosphine‐free Palladium Catalyst
- Short Synthesis of Sulfur Analogues of Polyaromatic Hydrocarbons through Three Palladium-Catalyzed C–H Bond Arylations
- Environmentally‐Safe Conditions for a Palladium‐Catalyzed Direct C3‐Arylation with High Turn Over Frequency of Imidazo[1,2‐b]pyridazines Using Aryl Bromides and Chlorides
- Direct access to 2-(hetero)arylated pyridines from 6-substituted 2-bromopyridines via phosphine-free palladium-catalyzed C–H bond arylations: the importance of the C6 substituent
- Reactivity of 1-(2-bromobenzyl)-4-halopyrazoles in intermolecular and intramolecular Pd-catalysed direct arylations
- Palladium-catalyzed direct desulfitative C2 arylations of 3-halo-N-protected indoles using (hetero)arenesulfonyl chlorides
- Reactivity of (poly)fluorobenzamides in palladium-catalysed direct arylations
- Asymmetrical 1,3‐Bis(heteroazolyl)benzene Platinum Complexes with Tunable Second‐Order Non‐Linear Optical Properties
- Palladium-catalysed direct arylation of heteroarenes using 1-(bromophenyl)-1,2,3-triazoles as aryl source
- Palladium-Catalysed Desulfitative Heck Reaction Tolerant to Aryl Carbon–Halogen Bonds for Access to (Poly)halo-Substituted Stilbene or Cinnamate Derivatives
- Regiocontroled Pd-catalysed C5-arylation of 3-substituted thiophene derivatives using a bromo-substituent as blocking group
- Reactivity of N-protected 5-(2-bromophenyl)tetrazoles in palladium-catalyzed direct arylation of heteroarenes or fluorobenzenes
- ChemInform Abstract: Palladium‐Catalyzed Direct Arylation Using Free‐Amine‐Substituted Polyfluoroanilines with Inhibition of Amination‐Type Reaction.
- ChemInform Abstract: Reactivity of 1‐(2‐Bromobenzyl)‐4‐halopyrazoles in Intermolecular and Intramolecular Pd‐Catalyzed Direct Arylations.
- Eco‐Friendly Solvents for Palladium‐Catalyzed Desulfitative CH Bond Arylation of Heteroarenes
- Pd‐Catalysed Direct Arylation of Heteroaromatics Using (Poly)halobenzenesulfonyl Chlorides as Coupling Partners: One Step Access to (Poly)halo‐Substituted Bi(hetero)aryls
- Palladium‐Catalyzed Iterative C−H Bond Arylations: Synthesis of Medium‐Size Heterocycles with a Bridgehead Nitrogen Atom
- Conditions for palladium-catalyzed direct arylations of 4-bromo and 4-iodo N-substituted pyrazoles without C–Br or C–I bond cleavage
- Synthesis of heteroarenes dyads from heteroarenes and heteroarylsulfonyl chlorides via Pd-catalyzed desulfitative C–H bond heteroarylations
- Reactivity of 3-(pyrrol-1-yl)thiophenes in Pd-catalysed direct arylations
- Palladium-catalyzed non-directed C–H bond arylation of difluorobenzenes and dichlorobenzenes bearing benzoxazole or benzothiazole
- Synthesis of symmetrical and unsymmetrical 1,3-diheteroarylbenzenes through palladium-catalyzed direct arylation of benzene-1,3-disulfonyl dichloride and 3-bromobenzenesulfonyl chlorides
- Cyclisation reaction between 3-methylquinoxaline-2-thione and benzaldehydes into 3-benzyl-2-aryl-thieno[2,3-b]quinoxaline promoted by Brønsted acids
- Conditions for the Palladium-Catalysed Direct 2-Arylation of 3-Bromobenzo[b]thiophene Tolerant of the Benzothienyl Carbon–Bromine Bond
- Efficient synthesis of π-conjugated molecules incorporating fluorinated phenylene units through palladium-catalyzed iterative C(sp2)–H bond arylations
- Palladium‐Catalysed Direct Arylation using Free‐Amine‐Substituted Polyfluoroanilines with Inhibition of Amination‐Type Reaction
- sp3–sp3 carbon–carbon bond formation using 2-alkylazoles and a bromoacrylate as the reaction partners
- ChemInform Abstract: Pd‐Catalyzed Direct Arylation of Heteroaromatics Using (Poly)halobenzenesulfonyl Chlorides as Coupling Partners: One Step Access to (Poly)halo‐Substituted Bi(hetero)aryls.
- ChemInform Abstract: Eco‐Friendly Solvents for Palladium‐Catalyzed Desulfitative C—H Bond Arylation of Heteroarenes.
- ChemInform Abstract: Formyl Substituent at C‐4 of Pyrazoles: A Temporary Protecting Group for Regioselective Palladium‐Catalyzed Direct Arylation at C‐5.
- ChemInform Abstract: Reactivity of 3‐(Pyrrol‐1‐yl)thiophenes in Pd‐Catalyzed Direct Arylations.
- Palladium-catalysed direct diarylations of pyrazoles with aryl bromides: a one step access to 4,5-diarylpyrazoles
- Formyl Substituent at C‐4 of Pyrazoles: A Temporary Protecting Group for Regioselective Palladium‐Catalyzed Direct Arylation at C‐5
- One pot Pd(OAc)2-catalysed 2,5-diarylation of imidazoles derivatives
- Benzenesulfonyl Chlorides: Alternative Coupling Partners for Regiocontrolled Palladium-Catalyzed Direct Desulfitative 5-Arylation of Furans
- Palladium-catalyzed 2,5-diheteroarylation of 2,5-dibromothiophene derivatives
- A Simple and Efficient Synthesis of (Hetero)Aryl-Substituted Benzothiazolyl or Benzoxazolyl Furan, Thiophene and N-methylpyrrole Derivatives through a Palladium-Catalyzed Regioselective C–H Bond Arylation
- Reactivity of bromofluorenes in palladium-catalysed direct arylation of heteroaromatics
- Pd-catalysed heteroarylations of 3-bromochromen-4-one via C–H bond activation of heteroarenes
- Palladium-catalysed direct regioselective C5-arylation of a thiophene bearing a cyclopropyl ketone group at C2
- Palladium‐Based Catalytic System for the Direct C3‐Arylation of Furan‐2‐carboxamides and Thiophene‐2‐carboxamides
- Isoquinoline Derivatives via Stepwise Regioselective sp2and sp3C–H Bond Functionalizations
- Catalytic System for Inhibition of Amination‐Type Reaction and Palladium‐Catalysed Direct Arylation using Non‐Protected Pyrazole Derivatives
- Palladium-catalyzed direct arylation using free NH2 substituted thiophene derivatives with inhibition of amination type reaction
- Palladium-catalysed direct arylations of heteroaromatics bearing dicyanovinyls at C2
- Palladium-Catalysed Direct Arylation of Heteroaromatics Using Unprotected Iodoanilines with Inhibition of the Amination Reaction
- ChemInform Abstract: Palladium‐Catalyzed Direct Arylation of Heteroaromatics Using Unprotected Iodoanilines with Inhibition of the Amination Reaction.
- ChemInform Abstract: Syntheses of New Benzoxazole Derivatives.
- Palladium‐Catalyzed Direct Arylations of Five‐Membered Heteroarenes Bearing N‐Monoalkylcarboxamide Substituents
- Palladium-catalysed direct arylations of heteroaromatics using more eco-compatible solvents pentan-1-ol or 3-methylbutan-1-ol
- Palladium‐Catalysed Direct Monoarylation of Bithiophenyl Derivatives or Bis(thiophen‐2‐yl)methanone with Aryl Bromides
- Syntheses of new benzoxazole derivatives
- ChemInform Abstract: Pd‐Catalyzed Direct 5‐Arylation of 1‐Methylpyrazole with Aryl Bromides.
- ChemInform Abstract: Palladium‐Catalyzed Direct Arylations of Heteroaromatics Using More Eco‐Compatible Solvents Pentan‐1‐ol or 3‐Methylbutan‐1‐ol.
- Palladium-catalyzed direct heteroarylation of chloropyridines and chloroquinolines
- Alkenyl bromides: useful coupling partners for the palladium-catalysed coupling with heteroaromatics via a C–H bond activation
- Palladium‐Catalysed Direct C‐H Activation/Arylation of Heteroaromatics: An Environmentally Attractive Access to Bi‐ or Polydentate Ligands
- Palladium-Tetraphosphine Complex Catalysed Heck Reaction of Vinyl Bromides with Alkenes: A Powerful Access to Conjugated Dienes
- Palladium/tetraphosphine catalyzed Heck reaction of vinyl bromides with alkenes: a powerful access to conjugated dienes
- Palladium-Catalyzed Direct C-H Activation / Arylation of Heteroaromatics: An Environmentally Attractive Access to Bi- or Polydentate Ligands
- Direct Arylation of Oxazole and Benzoxazole with Aryl or Heteroaryl Halides using a Palladium-Diphosphine Catalyst
- Direct arylation of oxazole and benzoxazole with aryl or heteroaryl halides using a palladium–diphosphine catalyst
- Direct Arylation of Thiophenes via Palladium‐Catalysed CH Functionalisation at Low Catalyst Loadings
- Heck Reactions of α‐ or β‐Substituted Enol Ethers with Aryl Bromides Catalysed by a Tetraphosphane/Palladium Complex – Direct Access to Acetophenone or 1‐Arylpropanone Derivatives
Revues de publication
- ChemInform × 10
- Tetrahedron × 8
- Tetrahedron Letters × 8
- European Journal of Organic Chemistry × 8
- Synthesis × 7
- ChemCatChem × 6
Publications par année
- 20261
- 20255
- 20242
- 20221
- 20212
- 20203
- 20197
- 20185
- 20178
- 201616
Collaborations
Établissements partenaires : Université Rennes 1 · University of Sfax · Faculty of Sciences of Sfax · University of Monastir · Mouloud Mammeri University of Tizi-Ouzou
Pays des co-auteurs : Tunisie · Algérie · Maroc
Co-auteurs
- Jean‐François Soulé
- Fazia Derridj
- Thierry Roisnel
- Ahmed Battace
- Maurice Santelli
- Kedong Yuan
- Anissa Beladhria
- Liqin Zhao
- Véronique Guerchais
- Mhamed Lemhadri
- Aymen Skhiri
- Nouria Laidaoui
Données bibliographiques issues d’OpenAlex (base ouverte).
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