ADDITIONSREAKTIONEN VON 2-THIAZOLIN-5-THIONEN MIT ACETYLENEN
- Other title
- REACTIONS D'ADDITION DE THIAZOLINE-2THIONES-5 AVEC LES COMPOSES ACETYLENIQUES (fr)
- Author
- JENNY C; OBRECHT D; HEIMGARTNER H
UNIV. ZUERICH, ORGANISCH-CHEMISCHES INST./ZUERICH 8057/CHE/(3 AUT.) - Source
- HELV. CHIM. ACTA; ISSN 0018-019X; CHE; DA. 1982; VOL. 65; NO 8; PP. 2583-2586; ABS. ENG; BIBL. 12 REF.
- Document type
- Article
- Language
- German
- Keyword (fr)
- PREPARATION ADDITION CHIMIQUE HETEROCYCLE SOUFRE AZOTE CYCLE 5 CHAINONS ISOMERISATION DITHIOLACTONE COMPOSE ACETYLENIQUE CETENES DITHIOACETAL TOLUENE!SUB REACTION THERMIQUE BUTYNEDIOIQUE ACIDE,ESTER DIMETHYLE!ENT PROPIOLIQUE ACIDE,ESTER ETHYLE!ENT ACETYLENE(DIPHENYL)!ENT THIAZOLINE-2THIONE-5(DIMETHYL-4,4 PHENYL-2)!ENT DITHIOLE-1,3 DICARBOXYLIQUE-4,5 ACIDE(ISOPROPYLIDENE-2) ESTER DIMETHYLE!FIN DITHIOLE-1,3 CARBOXYLIQUE-4 ACIDE(ISOPROPYLIDENE-2) ESTER ETHYLE!FIN THIOPHENEDICARBOXYLIQUE-2,3 ACIDE(DIHYDRO-4,5 DIMETHYL-4,4 THIOXO-5) ESTER DIMETHYLE!FIN THIOPHENECARBOXYLIQUE-3 ACIDE(DIHYDRO-4,5 DIMETHYL-4,4 THIOXO-5) ESTER METHYLE!FIN THIOPHENE(TETRAPHENYL)!FIN DITHIOLE-1,3CARBOXYLIQUE-4 ACIDE(PHENYL-1P ETHYLIDENE-2) ESTER ETHYLE!FIN THIAZOLINE-2THIONE-5(DIPHENYL-2,4 METHYL-4)!ENT CHIMIE ORGANIQUE
- Keyword (en)
- PREPARATION ADDITION REACTION SULFUR NITROGEN HETEROCYCLE FIVE MEMBERED RING SULFUR HETEROCYCLE ISOMERIZATION DITHIOLACTONE ACETYLENIC COMPOUND KETENES DITHIOACETAL TOLUENE!SUB THERMAL REACTION ORGANIC CHEMISTRY
- Keyword (es)
- QUIMICA ORGANICA
- Classification
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- PASCAL83X0146274
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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