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THE KINETICS AND MECHANISM OF ACID CATALYSED HYDROLYSIS OF LACTAMS

Author
WAN P; MODRO TA; YATES K
UNIV. TORONTO, DEP. CHEM./TORONTO ON M5S 1A1/CAN
Source
CAN. J. CHEM.; ISSN 0008-4042; CAN; DA. 1980; VOL. 58; NO 23; PP. 2423-2432; ABS. FRE; BIBL. 33 REF.
Document type
Article
Language
English
Keyword (fr)
CATALYSE ACIDE EFFET MILIEU TEMPERATURE PH CARBOXAMIDE REACTION MONOMOLECULAIRE HETEROCYCLE AZOTE CYCLE 4 CHAINONS CYCLE 5 CHAINONS CYCLE 6 CHAINONS CYCLE 7 CHAINONS PARAMETRE ACTIVATION EFFET STRUCTURE HYDROLYSE LACTAME ACETAMIDE(N-ETHYL) AZETIDINONE-2 PYRROLIDONE-2 PIPERIDONE-2 AZEPINONE-2(PERHYDRO) SULFURIQUE ACIDE!SUB CONSTANTE DISSOCIATION BASICITE CHIMIE ORGANIQUE
Keyword (en)
ACID CATALYSIS MEDIUM EFFECT TEMPERATURE CARBOXAMIDE MONOMOLECULAR REACTION NITROGEN HETEROCYCLE FOUR MEMBERED RING FIVE MEMBERED RING SIX MEMBERED RING SEVEN MEMBERED RING ACTIVATION PARAMETER STRUCTURE EFFECT HYDROLYSIS LACTAM PERHYDRO-2-AZEPINONE DISSOCIATION CONSTANT ALKALINITY 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
PASCAL8130245411

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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