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THE PROTONOTION OF SOME 5-SUBSTITUTED-3-NITRO-2-NN-DIMETHYLAMINOTHIOPHENS

Author
DE MARIA P; CONSIGLIO G; ARNONE C; SPINELLI D
UNIV. BOLOGNA, FAC. FARMACIA/BOLOGNA 40126/ITA
Source
C.S. PERKIN TRANSACTIONS 2; ISSN 0300-9580; GBR; DA. 1983; NO 4; PP. 481-484; BIBL. 27 REF.
Document type
Article
Language
English
Keyword (fr)
PROTONATION REACTION CHIMIQUE HETEROCYCLE SOUFRE CYCLE 6 CHAINONS FONCTION HAMMETT SOLUTION AQUEUSE PERCHLORIQUE ACIDE CONSTANTE DISSOCIATION EFFET ORTHO EFFET SUBSTITUANT ENERGIE LIBRE THIOPHENE(DIMETHYLAMINO-2 NITRO-3)!ENT THIOPHENE(BROMO-5 DIMETHYLAMINO-2 NITRO-3)!ENT THIOPHENECARBOXYLIQUE-2 ACIDE(DIMETHYLAMINO-5 NITRO-4) AMIDE!ENT THIOPHENECARBOXYLIQUE ACIDE(DIMETHYLAMINO-5 NITRO-4) ESTER METHYLE!ENT CHIMIE ORGANIQUE
Keyword (en)
PROTONATION CHEMICAL REACTION SULFUR HETEROCYCLE SIX MEMBERED RING HAMMETT FUNCTION AQUEOUS SOLUTION PERCHLORIC ACID DISSOCIATION CONSTANT ORTHO EFFECT SUBSTITUENT EFFECT FREE ENERGY 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
PASCAL83X0244600

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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