ACTIVATED NITRILES IN HETEROCYCLIC SYNTHESES. I: NOVEL SYNTHESIS OF PYRROLONES AND 1,2,4-TRIAZOL-3-OYL NITRILES
- Author
- MOHAMED RIFAAT HAMZA ELMOGHAYAR; MOHAMED KAMAL AHMED IBRAHIM; MAHMOUD MOHAMED MAHFOUZ RAMIZ; MOHAMED HILMY ELNAGDI
UNIV. CAIRO, FAC. SCI., DEP. CHEMISTRY/GIZA/EGY - Source
- ZEITSCHRIFT FUER NATURFORSCHUNG. TEIL B. ANORGANISCHE CHEMIE, ORGANISCHE CHEMIE; ISSN 0340-5087; DEU; DA. 1983; VOL. 38; NO 6; PP. 764-768; BIBL. 4 REF.
- Document type
- Article
- Language
- English
- Keyword (fr)
- HETEROCYCLE AZOTE CYCLE 5 CHAINONS REACTION CHIMIQUE SPECTRE IR SPECTRE RMN COMPOSE METHYLENE ACTIF LACTOSE HETEROCYCLE OXYGENE AZOTE SCISSION CYCLISATION CETONITRILE CYANOESTER DICETONE OXAZOLINE-2ONE-5(BENZYLIDENE-4 PHENYL-2)!ENT OXAZOLINE-2ONE-5(PHENYL-2 PHENYLAZO-4)!ENT PYRROLIDINECARBONITRILE-3(BENZYLIDENE-5 DIOXO-2,4)!FIN PYRROLINE-2CARBOXYLIQUE-3 ACIDE(AMINO-2 BENZYLIDENE-5 OXO-4) ESTER ETHYLE!FIN DESHYDROPHENYLALANINE(N-BENZOYL) ESTER!FIN NORVALINE(N-BENZOYL CYANO-4 OXO-5 PHENYL-5)!FIN TRIAZOLE-1,2,4ACRYLIQUE-3 ACIDE(ALPHA -CYANO DIPHENYL-1,5 BETA -HYDROXY) ESTER!FIN TRIAZOLE-1,2,4ACRYLONITRILE-3(ALPHA -BENZOYL DIPHENYL-1,5 BETA -HYDROXY)!FIN PYRAZOLO PYRIMIDINE DERIVE!FIN BENZENEPROPIONONITRILE(BETA -OXO)!ENT ACETIQUE ACIDE(CYANO) ESTER ETHYLE!ENT ACETYLACETONE!ENT HYDROGENE 1 CHIMIE ORGANIQUE
- Keyword (en)
- NITROGEN HETEROCYCLE FIVE MEMBERED RING CHEMICAL REACTION INFRARED SPECTRUM NMR SPECTRUM ACTIVE METHYLENE COMPOUND LACTOSE OXYGEN NITROGEN HETEROCYCLE SCISSION CYCLIZATION KETONITRILE CYANOESTER DIKETONE ORGANIC CHEMISTRY
- Keyword (es)
- QUIMICA ORGANICA
- Classification
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- PASCAL83X0356794
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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