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FORMATION OF SULPHUR COMPOUNDS IN HYDRODENITROGENATION OF QUINOLINE, 1,2,3,4-TETRAHYDROQUINOLINE, PYRIDINE, PIPERIDINE AND 1-PENT-4-ENYLAMINE ON A NICKEL-TUNGSTEN CATALYST IN THE PRESENCE OF HYDROGEN SULPHIDE

Author
CERNY M; TRKA A
CZECHOSLOVAK ACAD. SCI., INST. CHEMICAL PROCESS FUNDAMENTALS/PRAGUE 165 02/CSK
Source
COLLECTION OF CZECHOSLOVAK CHEMICAL COMMUNICATIONS; ISSN 0010-0765; CSK; DA. 1983; VOL. 48; NO 6; PP. 1749-1758; BIBL. 24 REF.
Document type
Article
Language
English
Keyword (fr)
HETEROCYCLE AZOTE COMPOSE ALTERNANT MECANISME REACTION COMPOSE BICYCLIQUE HETEROCYCLE SOUFRE COMPOSE AROMATIQUE NICKEL SULFURE!ACT CATALYSEUR MIXTE TUNGSTENE SULFURE!ACT CYCLE 6 CHAINONS THIOL REACTION THERMIQUE HYDROGENE SULFURE!ENT PYRIDINE!ENT QUINOLEINE!ENT QUINOLEINE(TETRAHYDRO-1,2,3,4)!ENT PIPERIDINE!ENT PENTENE-4YLAMINE-1!ENT BENZO (B) THIOPHENE(METHYL-2 PERHYDRO)!FIN THIOCHROMANNE(PERHYDRO)!FIN CYCLOPENTANETHIOL!FIN PENTANETHIOL-1!FIN THIOPHENE(METHYL-2 PERHYDRO)!FIN THIOPYRANNE(PERHYDRO)!FIN PENTYLE SULFURE!FIN PENTYLE DISULFURE!FIN THIOPYRANNE(PENTYL-2 PERHYDRO)!FIN SULFURE(PENTENE-4YL PENTYL)!FIN CYCLOHEXANETHIOL(ALLYL-2)!FIN BENZENE(PROPYL)!FIN CYCLOHEXANE(PROPYL)!FIN HYDRODESAZOTATION CHIMIE ORGANIQUE
Keyword (en)
NITROGEN HETEROCYCLE ALTERNANT COMPOUND REACTION MECHANISM BICYCLIC COMPOUND SULFUR HETEROCYCLE AROMATIC COMPOUND NICKEL SULFIDES!ACT MIXED CATALYST TUNGSTEN SULFIDES!ACT SIX MEMBERED RING THIOL THERMAL REACTION REACTION MECHANISM HYDROGEN SULFIDES!ENT PYRIDINE!ENT QUINOLINE!ENT ORGANIC CHEMISTRY
Keyword (es)
QUIMICA ORGANICA
Classification
Pascal
001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry

Discipline
Organic chemistry
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
PASCAL83X0442247

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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