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ZUM CYCLOADDITIONSVERHALTEN VON BIS(TRIFLUORMETHYL) SUBSTITUIERTEN NITRILYLIDEN. I: POSITIONSSELEKTIVITAET UND REGIOCHEMIE BEI ABFANGREAKTIONEN MIT HETEROKUMULENEN

Other title
COMPORTEMENT A LA CYCLOADDITION DES NITRILE YLURES BIS-TRIFLUOROMETHYL SUBSTITUES. I. SELECTIVITE DE POSITION ET REGIOCHIMIE DES REACTIONS DE PIEGEAGE PAR DES HETEROCUMULENES (fr)
Author
BURGER K; GOTH H; DALTROZZO E
TECH. UNIV. MUENCHEN, INST. ORGAN. CHEM./GARCHING 8046/DEU
Source
Z. NATURFORSCH., B; ISSN 0340-5087; DEU; DA. 1982; VOL. 37; NO 4; PP. 473-485; ABS. ENG; BIBL. 40 REF.
Document type
Article
Language
German
Keyword (fr)
CYCLOADDITION REACTION CHIMIQUE NITRILE YLURE PYROLYSE REACTION THERMIQUE DECYCLISATION INTERCEPTION HETEROCUMULENE ISOCYANATE ORGANIQUE SELECTIVITE HETEROCYCLE OXYGENE AZOTE PHOSPHORE CYCLE 5 CHAINONS HETEROCYCLE SOUFRE AZOTE SPECTRE RMN SPECTRE IR SPECTRE MASSE CARBONE DISULFURE!ENT OXAZAPHOSPHOLE-1,4,2ENE-4(BIS-TRIFLUOROMETHYL-3,3 TRIMETHOXY-2,2,2)!ENT AMMONIOMETHANURE(N-ALKYLIDYNE ALPHA ,ALPHA -BIS-TRIFLUOROMETHYL) ANILINE(N-SULFINYL)!ENT ISOCYANATE(PHENYL)!ENT CETENE(DIPHENYL)!ENT HETEROCYCLE AZOTE FLUOR 19 CHIMIE ORGANIQUE
Keyword (en)
CYCLOADDITION CHEMICAL REACTION NITRILE YLIDE PYROLYSIS THERMAL REACTION RING CLEAVAGE INTERCEPTION HETEROCUMULENE ORGANIC ISOCYANATE SELECTIVITY OXYGEN NITROGEN PHOSPHORUS HETEROCYCLE FIVE MEMBERED RING SULFUR NITROGEN HETEROCYCLE NMR SPECTRUM INFRARED SPECTRUM MASS SPECTRUM CARBON DISULFIDE!ENT 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
PASCAL82X0182929

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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