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ZUM REAKTIONSVERHALTEN VON TRIFLUORMETHYL-GRUPPEN: SYNTHESE VON 1,3-AZOLEN AUS TRIFLUORMETHYL-SUBSTITUIERTEN HETERO-1,3-DIENEN

Other title
REACTIVITE DES GROUPES TRIFLUOROMETHYLE: SYNTHESE D'AZOLES-1,3 A PARTIR D'HETERODIENES-1,3 SUBSTITUES PAR DES GROUPES TRIFLUOROMETHYLE (fr)
Author
BURGER K; OTTLINGER R; GOTH H; FIRL J
TECH. UNIV. MUENCHEN, ORGAN.-CHEM. INST./GARCHING 8046/DEU
Source
CHEM. BER.; ISSN 0009-2940; DEU; DA. 1982; VOL. 115; NO 7; PP. 2494-2507; ABS. ENG; BIBL. 57 REF.
Document type
Article
Language
German
Keyword (fr)
AMIDINE COMPOSE BENZENIQUE CARBOXAMIDE FLUOR COMPOSE ORGANIQUE HETEROCYCLE AZOTE HETEROCYCLE OXYGENE AZOTE HETEROCYCLE SOUFRE AZOTE CYCLE 5 CHAINONS SUBSTITUTION NUCLEOPHILE SPECTRE IR SPECTRE RMN STANNYLENE(DICHLORO)!ENT BENZAMIDE(N-PERFLUOROISOPROPYLIDENE)!ENT THIOBENZOIQUE ACIDE(FLUORO-4) PERFLUOROISOPROPYLIDENEAMIDE!ENT BENZIMIDIQUE ACIDE(N-(DIMETHYL-2,6 PHENYL)) PERFLUOROISOPROPYLIDENEAMIDE!ENT OXAZOLE(ARYL-2 FLUORO-5 TRIFLUOROMETHYL-4)!FIN THIAZOLE(ARYL-2 FLUORO-5 TRIFLUOROMETHYL-4)!FIN IMIDAZOLE(ARYL-1 FLUORO-5 PHENYL-2 TRIFLUOROMETHYL-4)!FIN OXAZOLINE-2(ARYL-2 DIFLUORO-5,5 DIFLUOROMETHYLENE-4)!FIN THIAZOLE(MORPHOLINO-5 P-TOLYL-2 TRIFLUOROMETHYL-4)!FIN HYDROGENE 1 FLUOR 19 CARBONE 13 CHIMIE ORGANIQUE
Keyword (en)
AMIDINE BENZENIC COMPOUND CARBOXAMIDE FLUORINE ORGANIC COMPOUNDS NITROGEN HETEROCYCLE OXYGEN NITROGEN HETEROCYCLE SULFUR NITROGEN HETEROCYCLE FIVE MEMBERED RING NUCLEOPHILIC SUBSTITUTION INFRARED SPECTRUM NMR SPECTRUM 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
PASCAL82X0281927

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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