المؤلفون: Florence Bonnaterre, Michèle Bois-Choussy, Jieping Zhu

المصدر: Beilstein Journal of Organic Chemistry, Vol 4, Iss 1, p 10 (2008)

مصطلحات موضوعية: Science, Organic chemistry, QD241-441

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1860-5397

URL الوصول: https://doaj.org/article/a63cf0737c0449759f6ad701b09522c5

المؤلفون: Thierry Convard, L.B. Lallos, Florence Bonnaterre, Valérie Bidau, Houcine Rahali, David Standring, Virginie Roques, Francois-Rene Alexandre, Maria Seifer, Anna-Giulia Loi, Damien Gloux, Christophe Claude Parsy, Elodie Rosinovsky, Dominique Chaves, Catherine Caillet, Frederic Leroy, Guillaume Brandt, Dominique Louis Nestor Ghislain Surleraux, Sylvie Cappelle, Yann Griffon, Simon Savin, Musiu Chiara, Laure Moulat, Michel Liuzzi, Michel Derock

المصدر: Bioorganic & Medicinal Chemistry Letters. 25:5427-5436

مصطلحات موضوعية: Macrocyclic Compounds, Serine Proteinase Inhibitors, medicine.medical_treatment, Hepatitis C virus, Clinical Biochemistry, Pharmaceutical Science, Hepacivirus, Viral Nonstructural Proteins, medicine.disease_cause, Biochemistry, Rats, Sprague-Dawley, Inhibitory Concentration 50, Mice, chemistry.chemical_compound, Drug Discovery, Hydrolase, medicine, Animals, Humans, Proline, Molecular Biology, Serine protease, chemistry.chemical_classification, NS3, Protease, Molecular Structure, biology, Organic Chemistry, Quinoline, Haplorhini, Virology, Rats, Enzyme, chemistry, Hepatocytes, Microsomes, Liver, biology.protein, Molecular Medicine

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e4b62addc3e995acb26693574bacaff
https://doi.org/10.1016/j.bmcl.2015.09.009

المؤلفون: Jieping Zhu, Florence Bonnaterre, Michèle Bois-Choussy

المساهمون: Institut de Chimie des Substances Naturelles (ICSN), Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)

المصدر: Beilstein Journal of Organic Chemistry, Vol 4, Iss 1, p 10 (2008)
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Beilstein-Institut, 2008, 4 (10), pp.1-11. ⟨10.3762/bjoc.4.10⟩

مصطلحات موضوعية: Stereochemistry, isocyanides and carboxylic acids followed by palladium-catalyzed cyclization), Amines Role: RCT (Reactant), chemistry.chemical_element, Sequence (biology), RACT (Reactant or reagent) (arom, prepn. (acyl)dihydrobenzoquinolinecarboxamides via Ugi reaction of iodobenzaldehydes with arylamines, 010402 general chemistry, 01 natural sciences, Full Research Paper, Catalysis, lcsh:QD241-441, lcsh:Organic chemistry, RACT (Reactant or reagent) (prepn. (acyl)dihydrobenzoquinolinecarboxamides via Ugi reaction of iodobenzaldehydes with arylamines, Molecule, lcsh:Science, ComputingMilieux_MISCELLANEOUS, 010405 organic chemistry, Chemistry, Drug discovery, [CHIM.ORGA]Chemical Sciences/Organic chemistry, Organic Chemistry, Cyclization, Ugi reaction (prepn. (acyl)dihydrobenzoquinolinecarboxamides via Ugi reaction of iodobenzaldehydes with arylamines, Combinatorial chemistry, Carboxylic acids, Isocyanides Role: RCT (Reactant), 0104 chemical sciences, acyldihydrobenzoquinolinecarboxamide prepn, iodobenzaldehydes arylamine isocyanide carboxylic acid Ugi reaction cyclization, Intramolecular force, Surface modification, lcsh:Q, Aldehydes Role: RCT (Reactant), human activities, Macromolecule, Palladium, RACT (Reactant or reagent) (aryl

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd3d5efb54c96619e94156de2c0a0df8
https://doaj.org/article/a63cf0737c0449759f6ad701b09522c5

المؤلفون: Michèle Bois-Choussy, Jieping Zhu, Florence Bonnaterre

المساهمون: Institut de Chimie des Substances Naturelles (ICSN), Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)

المصدر: Organic Letters
Organic Letters, American Chemical Society, 2006, 8(19), pp.4351-4354. ⟨10.1021/ol061755z⟩

مصطلحات موضوعية: carboxylic acid and isonitrile followed by copper-catalyzed Ullmann or microwave-assisted Buchwald-Hartwig amidation), Aldehydes Role: RCT (Reactant), RACT (Reactant or reagent) (halo, RACT (Reactant or reagent) (prepn. of oxindoles via Ugi four-component reaction of amine with iodobenzaldehyde, Iodide, Combined use, Sequence (biology), Coupling reaction catalysts (Ullmann, prepn. of oxindoles via Ugi four-component reaction of amine with iodobenzaldehyde, Amines, Carboxylic acids, Isocyanides Role: RCT (Reactant), 010402 general chemistry, 01 natural sciences, Biochemistry, Microwave assisted, Amides Role: RCT (Reactant), Addition reaction (Ugi, chemistry.chemical_compound, Amidation (Buchwald-Hartwig, PREP (Preparation), Rapid access, Organic chemistry, Oxindole, amine iodobenzaldehyde carboxylic acid isonitrile Ugi multicomponent addn palladium, iodophenylacetamide acylamino prepn intramol Ullmann coupling copper, acylamino iodophenylacetamide prepn intramol Buchwald Hartwig amidation microwave irradn, oxindole deriv prepn, indole oxo deriv prepn, copper intramol Ullmann coupling, palladium Ugi four component addn catalyst, Buchwald Hartwig amidation palladium catalyst, microwave irradn intramol Buchwald Hartwig amidation mediator, Physical and Theoretical Chemistry, chemistry.chemical_classification, Four component, 010405 organic chemistry, [CHIM.ORGA]Chemical Sciences/Organic chemistry, Aryl, Organic Chemistry, SPN (Synthetic preparation), General Medicine, arom, Combinatorial chemistry, Microwave (irradn, 0104 chemical sciences, iodo, chemistry, Intramolecular force, intramol, RACT (Reactant or reagent) (bisamides, Aromatic hydrocarbons Role: RCT (Reactant), Amidation catalysts, Ullmann reaction (prepn. of oxindoles via Ugi four-component reaction of amine with iodobenzaldehyde

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba9abbffa49c78c0db6dd8c272dbc62f
https://infoscience.epfl.ch/record/158102