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FORMATION OF NOVEL 1H-1,3-BENZODIAZEPINES IN THE PHOTOLYSIS OF ISOQUINOLINE N-IMIDES

Author
TSUCHIYA T; ENKAKU M; KURITA J; SAWANISHI H
HOKURIKU UNIV. SCH. PHARM., KANAZAWA 920-11, JPN
Source
J. CHEM. SOC., CHEM. COMMUNIC.; GBR; DA. 1979; NO 12; PP. 534-535; BIBL. 9 REF.
Document type
Article
Language
English
Keyword (fr)
HETEROCYCLE AZOTE COMPOSE BICYCLIQUE REACTION PHOTOCHIMIQUE YLURE CARBAMATE ORGANIQUE METHANE(DICHLORO)!SUB REACTION SIGMATROPE TRANSPOSITION AGRANDISSEMENT CYCLE PHOTOLYSE AMINIMIDE HYDROGENE CYANURE!FIN ISOQUINOLEINIOAMIDURE(ALPHA -ETHOXYCARBONYL,METHYL)!ENT ISOQUINOLEINIOAMIDURE(ALPHA -ETHOXYCARBONYL ETHOXYCARBONYL-1)!ENT BENZODIAZEPINE(ETHOXYCARBONYL METHYL)!FIN!ENT BENZODIAZEPINE(DIETHOXYCARBONYL)!FIN INDOLECARBOXYLIQUE-1 ACIDE(METHYL-2) ESTER ETHYLE!FIN BENZENECARBAMIQUE ACIDE(ACETAMIDO-2P ETHYL-2) ESTER ETHYLE!FIN CHIMIE PHYSIQUE CHIMIE GENERALE
Keyword (en)
NITROGEN HETEROCYCLE BICYCLIC COMPOUND PHOTOCHEMICAL REACTION YLIDE URETHANE SIGMATROPIC REACTION TRANSPOSITION RING EXPANSION PHOTOLYSIS AMINIMIDE PHYSICAL CHEMISTRY GENERAL CHEMISTRY
Keyword (es)
QUIMICA FISICA QUIMICA GENERAL
Classification
Pascal
001 Exact sciences and technology / 001C Chemistry / 001C01 General and physical chemistry

Discipline
General chemistry and physical chemistry
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
PASCAL8060012258

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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