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1
المؤلفون: Jieping Zhu, Artur Pinto, Luc Neuville
المساهمون: Institut de Chimie des Substances Naturelles (ICSN), Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)
المصدر: Tetrahedron Letters
Tetrahedron Letters, Elsevier, 2009, 50 (26), pp.3602-3605. ⟨10.1016/j.tetlet.2009.03.086⟩مصطلحات موضوعية: and alkynamide using palladium catalyst), Lactams Role: SPN (Synthetic preparation), Iodides Role: RCT (Reactant), PREP (Preparation) (bicyclic, prepn. of (arylmethylene)oxindoles by three-component coupling of aryl bromide, aryl halide alkynamide three component heterocyclization palladium catalyst, oxindole arylmethylene prepn, indolone arylmethylene prepn, chemistry.chemical_element, RACT (Reactant or reagent) (prepn. of (arylmethylene)oxindoles by three-component coupling of aryl bromide, 010402 general chemistry, 01 natural sciences, Biochemistry, Medicinal chemistry, Domino, Catalysis, chemistry.chemical_compound, Multicomponent reaction (three-component, RACT (Reactant or reagent) (iodides, Metalation (palladation, Drug Discovery, Organic chemistry, Oxindole, Bicyclic compounds Role: SPN (Synthetic preparation), ComputingMilieux_MISCELLANEOUS, PREP (Preparation) (lactams, [CHIM.ORGA]Chemical Sciences/Organic chemistry, 010405 organic chemistry, Amides Role: RCT (Reactant), RACT (Reactant or reagent) (aryl, Organic Chemistry, Arylation, Cyclization catalysts, Heterocyclization catalysts, Multicomponent reaction (prepn. of (arylmethylene)oxindoles by three-component coupling of aryl bromide, RACT (Reactant or reagent) (alpha, Bond formation, 0104 chemical sciences, 3. Good health, beta -unsatd, chemistry, aryl iodide, Aryl halides Role: RCT (Reactant), Aryl bromides Role: RCT (Reactant), Surface modification, Palladium
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2
المؤلفون: Karsten Meyer, Xile Hu
المصدر: Journal of Organometallic Chemistry. 690:5474-5484
مصطلحات موضوعية: for small mol. activation), Bond (carbon-metal, prepn. of, N-heterocyclic carbene complexes), Molecular structure, CAT (Catalyst use), chelators and prepn, Photochemistry, Biochemistry, Medicinal chemistry, five-membered, Coordination complex, (prepn. of tripodal N-heterocyclic carbene chelators and prepn, chemistry.chemical_compound, Insertion reaction, USES (Uses), PREP (Preparation), Materials Chemistry, tripodal NHC, prepn. of tripodal N-heterocyclic carbene, transition-metal complexes, prepn. of tripodal, PRP (Properties), RACT (Reactant or reagent) (polynuclear, chemistry.chemical_classification, RACT (Reactant or reagent) (first-row, Pi bond (back, Chelating agents, Density, tripodal nitrogen heterocyclic carbene prepn structure, SPN (Synthetic preparation), General Medicine, Carbene complexes, Group IB, MSC (Miscellaneous), (optimized, of tripodal N-heterocyclic carbene complexes), visual_art, RACT (Reactant or reagent) (nitrogen, RACT (Reactant or reagent) (prepn. of tripodal, Electrophile, visual_art.visual_art_medium, Ligands Role: PRP (Properties), structure DFT review, Metal ions in aqueous solution, Imine, Molecular structure (of tripodal, tripodal N-heterocyclic carbene chelators and prepn, activation, Metal, Inorganic Chemistry, element complexes Role: CAT (Catalyst use), Heterocyclic compounds Role: CAT, review, transition metal complex tripodal NHC prepn, RACT (Reactant or reagent) (multidentate, Reactivity (chemistry), Physical and Theoretical Chemistry, structure and bonding of their transition-metal complexes, RCT (Reactant), (Catalyst use), mol activation, copper complex tripodal nitrogen, Ligand, Aryl, Coordination compounds Role: CAT (Catalyst use), Molecules (small, Organic Chemistry, heterocyclic carbene prepn structure review, cobalt complex, functional theory, Electronic structure, Transition metal complexes Role, chemistry, Tripodal ligand, review tripodal nitrogen heterocyclic carbene ligand small, N-heterocyclic carbene chelators and prepn, Carbene
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3
المؤلفون: Jieping Zhu, Aude Fayol
المصدر: Organic Letters. 6:115-118
مصطلحات موضوعية: chemistry.chemical_classification, Amines Role: RCT (Reactant), Organic Chemistry, and alpha -isocyano acetamides), General Medicine, Ring (chemistry), RACT (Reactant or reagent) (alkynyl, prepn. of polysubstituted tetrahydrofuropyridines via three-component condensation of amino pentynoate, Biochemistry, Toluene, Medicinal chemistry, Aldehyde, Coupling reaction (three-component, chemistry.chemical_compound, chemistry, Aldehydes, Isocyanides Role: RCT (Reactant), aldehydes, furopyridine tetrahydro polysubstituted prepn, aldehyde three component condensation aminopentynoate isocyanoacetamide, Organic chemistry, RACT (Reactant or reagent) (prepn. of polysubstituted tetrahydrofuropyridines via three-component condensation of amino pentynoate, Ammonium chloride, Physical and Theoretical Chemistry
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4Academic Journal
المؤلفون: STEELE, REBECCA MARY, C. Monti, C.M.A. Gennari, U. Piarulli, F. Andreoli, N. Vanthuyne, C. Roussel
المساهمون: R.M. Steele, C. Monti, C.M.A. Gennari, U. Piarulli, F. Andreoli, N. Vanthuyne, C. Roussel
مصطلحات موضوعية: Cyanohydrins Role : SPN (Synthetic preparation), PREP (Preparation) (O-acetyl and O-trimethylsilyl, prepn. of a-trimethylsiloxy and a-acetyloxy nitriles using the enantioselective cyanosilylation of aldehydes with trimethylsilyl cyanide in the presence of atropisomeric thiourea catalysts), Atropisomers (a mixt. of atropisomeric thioureas is more effective as a catalyst for the enantioselective cyanosilylation of aldehydes with trimethylsilyl cyanide than sepd. thiourea atropisomers), Rotational barrier (prepn. of atropisomeric thioureas as catalysts for the enantioselective cyanosilylation of aldehydes with trimethylsilyl cyanide and the barrier to rotation of an (aminophenyl)thiazolinethione intermediate), Asymmetric synthesis and induction (prepn. of a-(trimethylsiloxy)nitriles and a-(acetyloxy)nitriles using the enantioselective cyanosilylation of aldehydes with trimethylsilyl cyanide in the presence of atropisomeric thiourea catalysts), Thioureas Role : PEP (Physical, engineering or chemical process), PRP (Properties), PUR (Purification or recovery), PYP (Physical process), RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), PROC (Process), RACT (Reactant or reagent) (prepn. of a-(trimethylsiloxy)nitriles and a-(acetyloxy)nitriles using the enantioselective cyanosilylation of aldehydes with trimethylsilyl cyanide in the presence of atropisomeric thiourea catalysts), Aldehydes Role : RCT (Reactant), RACT (Reactant or reagent)(prepn. of a-(trimethylsiloxy)nitriles and a-(acetyloxy)nitriles using the enantioselective cyanosilylation of aldehydes with trimethylsilyl cyanide in the presence of atropisomeric thiourea catalysts), Addition reaction, Addition reaction catalysts (stereoselective, cyanosilylation, prepn. of a-(trimethylsiloxy)nitriles and a-(acetyloxy)nitriles using the enantioselective cyanosilylation of aldehydes with trimethylsilyl cyanide in the presence of atropisomeric thiourea catalysts), Settore CHIM/06 - Chimica Organica
Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000237753900018; volume:17; issue:6; firstpage:999; lastpage:1006; journal:TETRAHEDRON-ASYMMETRY; http://hdl.handle.net/2434/22063; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-33646489511
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5
المؤلفون: Tracey Pirali, Gian Cesare Tron, Jieping Zhu, Géraldine Masson
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, 2007, 9 (25), pp.5275-5278. ⟨10.1021/ol7024372⟩مصطلحات موضوعية: Macrocyclic Compounds, RACT (Reactant or reagent) (prepn. of iminooxazolines via ammonium chloride-promoted three-component reaction of isocyanoacetamides, Carboxylic Acids, aldehydes and amino alcs.), Ugi reaction (prepn. of isocyanoacetamides via Ugi reaction of ketones, Alpha (ethology), iminooxazoline prepn three component reaction isocyanoacetamide aldehyde amino alc, macrocyclodepsipeptide prepn iminooxazoline sapon cyclization, [SDV.BC]Life Sciences [q-bio]/Cellular Biology, 010402 general chemistry, 01 natural sciences, Biochemistry, Medicinal chemistry, Aldehyde, Ammonium Chloride, PREP (Preparation) (depsipeptides, chemistry.chemical_compound, PREP (Preparation) (prepn. of macrocyclodepsipeptides via cyclization of iminooxazolines), Multicomponent reaction (three-component, prepn. of iminooxazolines via ammonium chloride-promoted three-component reaction of isocyanoacetamides, Depsipeptides, Acetamides, Organic chemistry, Physical and Theoretical Chemistry, RACT (Reactant or reagent) (prepn. of isocyanoacetamides via Ugi reaction of ketones, Oxazoles, 5-iminooxazoline, chemistry.chemical_classification, Molecular Structure, 010405 organic chemistry, Chemistry, Component (thermodynamics), Hydrolysis, Peptides Role: SPN (Synthetic preparation), Organic Chemistry, Alcohols Role: RCT (Reactant), RACT (Reactant or reagent) (amino, 0104 chemical sciences, Transformation (genetics), ammonium formate and isocyanoacetates), Cyclization (prepn. of macrocyclodepsipeptides via cyclization of iminooxazolines), Macrocyclic compounds Role: SPN (Synthetic preparation), Cyanamide, Cyclization, macrocyclic, prepn. of macrocyclodepsipeptides via cyclization of iminooxazolines), Aldehydes Role: RCT (Reactant), Ketones Role: RCT (Reactant), Ammonium chloride, Acids
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6Academic Journal
المؤلفون: Wagner, Tobias, Lange, Jens, Grote, Dirk, Sander, Wolfram, Schaumann, Ernst, Adiwidjaja, Gunadi, Adam, Arnold, Kopf, Jürgen
المصدر: European journal of organic chemistry
مصطلحات موضوعية: ddc:540, Alkenes Role: RCT (Reactant), RACT (Reactant or reagent) (prepn., structural characterization, and reactivity of organylthio(silyl)carbenes), Carbenes, Crystal Structure, Cycloaddition reaction (stereoselective), Diazo compounds Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), Elimination reaction, Molecular structure (optimized, Molecular structure (prepn., prepn.
وصف الملف: 5198–5207
Relation: urn:issn:1434-193X
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7Academic Journal
المؤلفون: Kuchta, Matthew C., Gemel, Christian, Metzler-Nolte, Nils
المصدر: Journal of organometallic chemistry
مصطلحات موضوعية: ddc:540, Amino acids Role: RCT (Reactant), RACT (Reactant or reagent) (prepn. and structure of an amino acid bioconjugate of an trimethylplatinum tris(pyrazolyl)borate complex), Coupling reaction, Crystal Structure, Ligands Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), Molecular structure
وصف الملف: 1310–1314
Relation: urn:issn:0022-328X
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8
المؤلفون: William Erb, Luc Neuville, Jieping Zhu
المساهمون: Institut de Chimie des Substances Naturelles (ICSN), Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)
المصدر: Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2009, 74 (8), pp.3109-15. ⟨10.1021/jo900210x⟩مصطلحات موضوعية: Indoles, Magnetic Resonance Spectroscopy, Intramolecular reaction, MESH: Solvents, Ligands, 01 natural sciences, Medicinal chemistry, Dioxanes, chemistry.chemical_compound, aldehydes and isocyanides followed by palladium-XPhos-catalyzed heterocyclization under microwave irradn.), Heterocyclization (prepn. of benzopiperazinone derivs. via four-component Ugi addn. of iodoarylamines with carboxylic acids, MESH: Structure-Activity Relationship, Amide, benzopiperazinone deriv prepn, iodophenylaminocarboxamide prepn heterocyclization palladium XPhos, oxindole deriv prepn, palladium BINAP heterocyclization iodophenylaminocarboxamide, MESH: Ligands, MESH: Cyclization, Microwaves, BINAP, MESH: Indoles, Molecular Structure, Chemistry, Ugi reaction (four-component, prepn. of benzopiperazinone derivs. via four-component Ugi addn. of iodoarylamines with carboxylic acids, Lactam, MESH: Palladium, Palladium, Reaction mechanism, RACT (Reactant or reagent) (aryl, Stereochemistry, MESH: Molecular Structure, [SDV.BC]Life Sciences [q-bio]/Cellular Biology, MESH: Microwaves, 010402 general chemistry, Catalysis, Microwave (irradn, Structure-Activity Relationship, MESH: Quinoxalines, XPhos, Quinoxalines, RACT (Reactant or reagent) (prepn. of benzopiperazinone derivs. via four-component Ugi addn. of iodoarylamines with carboxylic acids, MESH: Dioxanes, Amines Role: RCT (Reactant), 010405 organic chemistry, Ligand, MESH: Magnetic Resonance Spectroscopy, Organic Chemistry, Aldehydes, Carboxylic acids, Isocyanides Role: RCT (Reactant), MESH: Catalysis, 0104 chemical sciences, Oxindoles, Cyclization, Solvents, Ugi reaction
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9
المؤلفون: Luc Neuville, Jieping Zhu, Sébastien Bénard
المساهمون: Institut de Chimie des Substances Naturelles (ICSN), Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)
المصدر: Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2008, 73 (16), pp.6441-4. ⟨10.1021/jo801033y⟩مصطلحات موضوعية: Azoles, Cyclopropanes, and sulfonamides via copper-mediated coupling of cyclopropylboronic acid with parent compds.), Amides Role: RCT (Reactant), Copper(II) acetate, Heterocyclic compounds Role: SPN (Synthetic preparation), medicine.drug_class, Copper mediated, education, chemistry.chemical_element, Carboxamide, Acetates, 010402 general chemistry, 01 natural sciences, RACT (Reactant or reagent) (prepn. of N-cyclopropyl derivs. of azoles, chemistry.chemical_compound, Transition metal, PREP (Preparation) (N-cyclopropyl, prepn. of N-cyclopropyl derivs. of azoles, Amides Role: SPN (Synthetic preparation), medicine, Organic chemistry, chemistry.chemical_classification, Sulfonamides, 010405 organic chemistry, [CHIM.ORGA]Chemical Sciences/Organic chemistry, PREP (Preparation) (nitrogen, Organic Chemistry, Boronic Acids, Copper, 0104 chemical sciences, 3. Good health, Sulfonamide, amides, Dichloroethane, Heterocyclic compounds Role: RCT (Reactant), azole cyclopropylboronic acid copper acetate bipyridine N cyclopropylation, cyclopropylazole deriv prepn, amide cyclopropylboronic acid copper acetate bipyridine coupling, cyclopropylamide deriv prepn, sulfonamide cyclopropylboronic acid copper acetate bipyridine N alkylation, cyclopropylsulfonamide deriv prepn, N-cyclopropyl, chemistry, Cyclization, Alkylation (N-cyclopropylation, RACT (Reactant or reagent) (nitrogen, Sodium carbonate
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10
المؤلفون: Jieping Zhu, Angela Salcedo, Luc Neuville
المساهمون: Institut de Chimie des Substances Naturelles (ICSN), Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)
المصدر: Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2008, 73 (9), pp.3600-3. ⟨10.1021/jo800266y⟩مصطلحات موضوعية: inorganic chemicals, Ugi adduct copper intramol arylation, benzoxazolylmethyl iodobenzamide deriv prepn palladium intramol arylation, isoindolinone benzoxazolyl deriv prepn, intramol arylation catalyst palladium, Indoles, Intramolecular reaction, education, chemistry.chemical_element, [SDV.BC]Life Sciences [q-bio]/Cellular Biology, Ligands, 010402 general chemistry, 01 natural sciences, Chemical synthesis, Medicinal chemistry, Catalysis, Amides Role: RCT (Reactant), PREP (Preparation), Molecule, Organic chemistry, RACT (Reactant or reagent) (bisamides, prepn. of (benzoxazolyl)isoindolinones via copper-catalyzed intramol. O-arylation of Ugi adducts followed by palladium-catalyzed intramol. C-arylation), Arylation, Arylation catalysts (intramol, Heterocyclization, Heterocyclization catalysts, Ugi reaction (prepn. of (benzoxazolyl)isoindolinones via copper-catalyzed intramol. O-arylation of Ugi adducts followed by palladium-catalyzed intramol. C-arylation), Aldehydes Role: RCT (Reactant), Molecular Structure, RACT (Reactant or reagent) (prepn. of (benzoxazolyl)isoindolinones via copper-catalyzed intramol. O-arylation of Ugi adducts followed by palladium-catalyzed intramol. C-arylation), Amines Role: RCT (Reactant), 010405 organic chemistry, Organic Chemistry, SPN (Synthetic preparation), Benzene, Amides, Carbon, 0104 chemical sciences, chemistry, RACT (Reactant or reagent) (primary, Intramolecular force, Ugi reaction, Azo Compounds, Copper, Palladium
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11
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
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12
المؤلفون: Carine Bughin, Jieping Zhu, Géraldine Masson
المساهمون: Institut de Chimie des Substances Naturelles (ICSN), Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC), Institut de neurosciences cognitives de la méditerranée - UMR 6193 (INCM), Université de la Méditerranée - Aix-Marseille 2-Centre National de la Recherche Scientifique (CNRS), Pathologie et virologie moléculaire (PVM (UMR_7151)), Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris Diderot - Paris 7 (UPD7), University of California [Riverside] (UCR), University of California, Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Université Paris Diderot - Paris 7 (UPD7)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), University of California [Riverside] (UC Riverside), University of California (UC)
المصدر: Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2007, 72 (5), pp.1826-9. ⟨10.1021/jo0621874⟩
Journal of Organic Chemistry, 2007, 72 (5), pp.1826-9. ⟨10.1021/jo0621874⟩مصطلحات موضوعية: Magnetic Resonance Spectroscopy, MESH: Amino Acids, Spectrophotometry, Infrared, cyclic, prepn. of cyclodepsipeptides via three-component cyclocondensation of sugar amino acid or sugar amino alc. with aldehydes and isonitriles followed by macrocyclization as key steps), Cyclocondensation reaction, Macrocyclization (prepn. of cyclodepsipeptides via three-component cyclocondensation of sugar amino acid or sugar amino alc. with aldehydes and isonitriles followed by macrocyclization as key steps), Aldehydes Role: RCT (Reactant), Alcohol, MESH: Solvents, 01 natural sciences, Aldehyde, Mass Spectrometry, chemistry.chemical_compound, Sugar Alcohols, Depsipeptides, PREP (Preparation), Organic chemistry, Amino Acids, MESH: Cyclization, chemistry.chemical_classification, MESH: Indicators and Reagents, SPN (Synthetic preparation), Amino Alcohols, Cyclic peptide, Amino acid, MESH: Chromatography, Thin Layer, Aminosugar, cyclodepsipeptide prepn, sugar amino acid aldehyde isonitrile three component cyclocondensation macrocyclization, Stereochemistry, RACT (Reactant or reagent) (sugar, Multicomponent reaction (three-component, RACT (Reactant or reagent) (amino, 010402 general chemistry, MESH: Acids, MESH: Amino Alcohols, PREP (Preparation) (depsipeptides, MESH: Sugar Alcohols, Trifluoroacetic acid, [SDV.BBM]Life Sciences [q-bio]/Biochemistry, Molecular Biology, Sugar, MESH: Mass Spectrometry, Dipeptide, sugar, Peptides Role: SPN (Synthetic preparation), 010405 organic chemistry, MESH: Spectrophotometry, Infrared, MESH: Magnetic Resonance Spectroscopy, Organic Chemistry, MESH: Depsipeptides, Alcohols Role: RCT (Reactant), 0104 chemical sciences, chemistry, Cyclization, RACT (Reactant or reagent) (prepn. of cyclodepsipeptides via three-component cyclocondensation of sugar amino acid or sugar amino alc. with aldehydes and isonitriles followed by macrocyclization as key steps), Amino acids Role: RCT (Reactant), Solvents, Indicators and Reagents, Chromatography, Thin Layer, Acids
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13
المؤلفون: Pascal Retailleau, Christophe Rondot, Jieping Zhu
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, 2007, 9(2), pp.247-250. ⟨10.1021/ol0627202⟩مصطلحات موضوعية: Models, Molecular, Magnetic Resonance Spectroscopy, Stereochemistry, Crystal structure, Crystallography, X-Ray, Imides, 010402 general chemistry, Sensitivity and Specificity, Biochemistry, 01 natural sciences, Benzylic alcohol, SN1 reaction, Nucleophile, PREP (Preparation), Molecular structure (of allyloxyphenyl heterocyclic derivs.), Hydrolysis (prepn. and hydrolysis of chiral dihydrooazines from arylaminopropane diols via bistrichloroacetimidate intermediates), Stereoselective synthesis (prepn. of chiral dihydrooazines from arylaminopropane diols via bistrichloroacetimidate intermediates), Heterocyclic compounds Role: PRP (Properties), Chloroacetates, Trichloroacetic Acid, Physical and Theoretical Chemistry, asym synthesis dihydrooxazine deriv cyclization bistrichloroacetimidate intermediate, mol crystal structure dihydro oxazine deriv, diaminoalc prepn, ComputingMilieux_MISCELLANEOUS, RCT (Reactant), Molecular Structure, 010405 organic chemistry, Chemistry, [CHIM.ORGA]Chemical Sciences/Organic chemistry, Organic Chemistry, Substitution (logic), Leaving group, Absolute configuration, Stereoisomerism, SPN (Synthetic preparation), General Medicine, Amino Alcohols, RACT (Reactant or reagent) (prepn. of chiral dihydrooazines from arylaminopropane diols via bistrichloroacetimidate intermediates), Glycols Role: RCT (Reactant), 0104 chemical sciences, Cyclization, Intramolecular force, Vicinal, Cyclization (regioselective, prepn. of chiral dihydrooazines from arylaminopropane diols via bistrichloroacetimidate intermediates), Cyclization (stereoselective
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14
المؤلفون: Hisanori Nambu, Erick M. Carreira, Jerome Waser, Boris Gaspar
المصدر: Journal of the American Chemical Society. 128(35)
مصطلحات موضوعية: Azides, Double bond, Alkenes, Biochemistry, Catalysis, Sulfone, chemistry.chemical_compound, Colloid and Surface Chemistry, RACT (Reactant or reagent) (prepn. of hydrazines and azides via the metal-catalyzed hydrohydrazination and hydroazidation of olefins), Hydrazides Role: SPN (Synthetic preparation), Organic chemistry, Alkyl, Amination, chemistry.chemical_classification, Sulfonyl, Manganese, Molecular Structure, Alkene, PREP (Preparation) (prepn. of hydrazines and azides via the metal-catalyzed hydrohydrazination and hydroazidation of olefins), General Medicine, General Chemistry, Cobalt, Addition reaction (prepn. of hydrazines and azides via the metal-catalyzed hydrohydrazination and hydroazidation of olefins), Alkenes Role: RCT (Reactant), Combinatorial chemistry, Hydrazines, chemistry, Models, Chemical, Reagent, Functional group, Hydrazoic acid, alkene hydroazination hydroazidation azide hydrazine prepn, Azide
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15
المصدر: ChemInform. 37
مصطلحات موضوعية: Allylic rearrangement, chemistry.chemical_element, Alkenes, Hydroxylation, Biochemistry, Medicinal chemistry, Catalysis, Organic chemistry, Physical and Theoretical Chemistry, PREP (Preparation) (unsatd, prepn. of allylic and propargylic hydrazides by cobalt-catalyzed hydrohydrazination of dienes and enynes), Alkadienes, Addition reaction, Molecular Structure, Addition reaction catalysts (prepn. of allylic and propargylic hydrazides by cobalt-catalyzed hydrohydrazination of dienes and enynes), Alkenynes Role: RCT (Reactant), Organic Chemistry, Water, Regioselectivity, Stereoisomerism, Cobalt, General Medicine, Hydrazines, chemistry, RACT (Reactant or reagent) (prepn. of allylic and propargylic hydrazides by cobalt-catalyzed hydrohydrazination of dienes and enynes), Hydrazides Role: SPN (Synthetic preparation), hydrazide allyl propargyl prepn hydrohydrazination alkadiene alkenyne
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16
المؤلفون: Damien Bonne, Jieping Zhu, Mouloud Dekhane
المصدر: Journal of the American Chemical Society. 127(19)
مصطلحات موضوعية: Reaction mechanism, Hydrochloride, and alpha -isocyano phenylacetate as reactants), amine salt, Biochemistry, Aldehyde, Redox, Catalysis, Adduct, chemistry.chemical_compound, Acetic acid, Homologation, Oxidation (prepn. of amides via mild, Colloid and Surface Chemistry, Amide, oxidative one-carbon homologation using aldehyde, mild oxidative one carbon homologation aldehyde amide prepn, aldehyde homologation oxidn amine salt isocyano phenylacetate, Organic chemistry, RACT (Reactant or reagent) (prepn. of amides via mild, Amides Role: SPN (Synthetic preparation), Dimethylamine, chemistry.chemical_classification, PREP (Preparation) (prepn. of amides via mild, General Chemistry, General Medicine, Aldehydes Role: RCT (Reactant), chemistry, Reagent
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17
المؤلفون: Aude Fayol, Jieping Zhu
المصدر: Organic letters. 7(2)
مصطلحات موضوعية: Indoles, amines, Biochemistry, Aldehyde, chemistry.chemical_compound, and aldehydes), Isocyanides Role: RCT (Reactant), PREP (Preparation), Organic chemistry, Molecule, Physical and Theoretical Chemistry, chemistry.chemical_classification, Aza Compounds, Molecular Structure, Component (thermodynamics), Organic Chemistry, SPN (Synthetic preparation), General Medicine, Combinatorial chemistry, Toluene, RACT (Reactant or reagent) (prepn. of 6-azaindolines and pyrrolidinone-fused 6-azaindolines by three-component reaction of isocyanoacetamides, External energy, chemistry, Chemical bond, azaindoline pyrrolidinone fused prepn, three component reaction isocyanoacetamide amine aldehyde, Aldehydes, Amines Role: RCT (Reactant), Amine gas treating, Cyclization (prepn. of 6-azaindolines and pyrrolidinone-fused 6-azaindolines by three-component reaction of isocyanoacetamides, Heterocyclic Compounds, 3-Ring, Tricyclic
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18
المؤلفون: Mouloud Dekhane, Damien Bonne, Jieping Zhu
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, 2005, 7 (23), pp.5285-5288. ⟨10.1021/ol052239w⟩مصطلحات موضوعية: benzoxazine imino multicomponent synthesis, benzamide isocyano prepn three component coupling aldehyde amine, isonitrile amide prepn three component coupling aldehyde amine, 010402 general chemistry, Biochemistry, 01 natural sciences, Aldehyde, RACT (Reactant or reagent) (aryl, prepn. of aminoalkyl-substituted (imino)benzoxazines and derivs. via three-component coupling of o-isocyanobenzamides with aldehydes and amines), Amines Role: RCT (Reactant), RACT (Reactant or reagent) (aliph, Amides Role: RCT (Reactant), chemistry.chemical_compound, Polymer chemistry, PREP (Preparation), Organic chemistry, Reactivity (chemistry), Physical and Theoretical Chemistry, ComputingMilieux_MISCELLANEOUS, chemistry.chemical_classification, 010405 organic chemistry, Component (thermodynamics), [CHIM.ORGA]Chemical Sciences/Organic chemistry, Organic Chemistry, SPN (Synthetic preparation), RACT (Reactant or reagent) (prepn. of aminoalkyl-substituted (imino)benzoxazines and derivs. via three-component coupling of o-isocyanobenzamides with aldehydes and amines), Coupling reaction (three-component, General Medicine, Isocyanides Role: RCT (Reactant), Toluene, 3. Good health, 0104 chemical sciences, chemistry, Amine gas treating, Ammonium chloride, Aldehydes Role: RCT (Reactant), Stoichiometry
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19Academic Journal
المؤلفون: Bragg, Ryan A., Clayden, Jonathan, Menet, Christel J.
المصدر: Bragg , R A , Clayden , J & Menet , C J 2002 , ' 'meso-Selective' functionalisation of N-benzyl-α-methylbenzylamine derivatives by α-lithiation and alkylation ' , Tetrahedron Letters , vol. 43 , no. 11 , pp. 1955-1959 . https://doi.org/10.1016/S0040-4039(02)00154-5
مصطلحات موضوعية: Bond cleavage (oxidative, prepn. of phenylglycines via diastereoselective reactions of organolithium methylbenzylamine derivs.), Asymmetric synthesis and induction, Carboxylation, Lithiation, Methylation, Stereochemistry, Transmetalation (prepn. of phenylglycines via diastereoselective reactions of organolithium methylbenzylamine derivs.), Amides, Amino acids Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. of phenylglycines via diastereoselective reactions of organolithium methylbenzylamine derivs.), Metalation (stannylation
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20
المؤلفون: Jieping Zhu, Jérôme Blanchet
المساهمون: Institut de Chimie des Substances Naturelles (ICSN), Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)
المصدر: Tetrahedron Letters
Tetrahedron Letters, Elsevier, 2004, 45 (23), pp.4449-4452. ⟨10.1016/j.tetlet.2004.04.055⟩مصطلحات موضوعية: 010402 general chemistry, Biochemistry, 01 natural sciences, Aldehyde, chemistry.chemical_compound, Drug Discovery, PREP (Preparation), Organic chemistry, RACT (Reactant or reagent) (prepn. of iminothiazolidinones via nucleophilic addn. of chloroform to aldehydes followed by Reeve's reaction with thioureas), Coupling reaction (three-component, prepn. of iminothiazolidinones via nucleophilic addn. of chloroform to aldehydes followed by Reeve's reaction with thioureas), Heterocyclization (Reeve's reaction, Aldehydes Role: RCT (Reactant), Alkyl, ComputingMilieux_MISCELLANEOUS, chemistry.chemical_classification, Chloroform, 010405 organic chemistry, Component (thermodynamics), [CHIM.ORGA]Chemical Sciences/Organic chemistry, Aryl, Organic Chemistry, SPN (Synthetic preparation), General Medicine, 0104 chemical sciences, Thiourea, chemistry, Alcohols Role: RCT (Reactant), 4-thiazolidinone, aldehyde chloroform nucleophilic addn, chloromethylcarbinol prepn thiourea Reeve synthesis, iminothiazolidinone prepn Reeve synthesis