STUDIES ON NITRILE IMINES. SYNTHESIS OF SOME NEW FIVE-MEMBERED HETEROCYCLICS VIA N-(2,4-DINITROPHENYL)-C-ALKYL NITRILE IMINES
- Author
- TEWARI RS; DIXIT PD; PARIHAR P
HARCOURT BUTLER TECHNOLOGICAL INST./KANPUR 2/IND - Source
- JOURNAL OF HETEROCYCLIC CHEMISTRY; ISSN 0022-152X; USA; DA. 1982; VOL. 19; NO 6; PP. 1573-1575; BIBL. 8 REF.
- Document type
- Article
- Language
- English
- Keyword (fr)
- NITRILIMINE REACTION CONCERTEE SPECTRE IR SPECTRE RMN HETEROCYCLE AZOTE CYCLE 5 CHAINONS BENZENE!SUB CYCLOADDITION EFFET STERIQUE HETEROCYCLE OXYGENE AZOTE ALDIMINE ALDEHYDE COMPOSE ACETYLENIQUE YLURE ACIDE CARBOHYDRAZONIQUE BENZALDEHYDE DERIVE!ENT BENZALDEHYDE,PHENYLIMINE!ENT BUTYNEDIOIQUE ACIDE,ESTER DIMETHYLE!ENT AMMONIOAMIDURE(N-ALKYLIDYNE ALPHA -(DINITRO-2,4 PHENYL)) PROPIONOHYDRAZONIQUE ACIDE(N-(DINITRO-2,4 PHENYL)) CHLORURE!ENT BUTYROHYDRAZONIQUE ACIDE(N-(DINITRO-2,4 PHENYL)) CHLORURE!ENT ISOBUTYROHYDRAZONIQUE ACIDE(N-(DINITRO-2,4 PHENYL)) CHLORURE!ENT TRIAZOLE-1,2,4INE-2(ALKYL-3 DINITRO-2P,4P PHENYL-1 DIPHENYL-4,5)!FIN OXADIAZOLE-1,3,4INE-2(ALKYL-2 ARYL-5 DINITRO-2P,4P PHENYL-4)!FIN PYRAZOLEDICARBOXYLIQUE-4,5 ACIDE(ALKYL-3 DINITRO-2P,4P PHENYL-1) ESTER DIMETHYLE!FIN TRIETHYLAMINE!ACT HYDROGENE 1 CHIMIE ORGANIQUE
- Keyword (en)
- NITRILIMINE CONCERTED REACTION INFRARED SPECTRUM NMR SPECTRUM NITROGEN HETEROCYCLE FIVE MEMBERED RING BENZENE!SUB CYCLOADDITION STERIC EFFECT OXYGEN NITROGEN HETEROCYCLE ALDIMINE ALDEHYDE ACETYLENIC COMPOUND YLIDE BENZENE!SUB CARBOHYDRAZONIC ACID ORGANIC CHEMISTRY
- Keyword (es)
- QUIMICA ORGANICA
- Classification
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- PASCAL83X0191339
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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