ALPHA -ISOTHIOCYANATOACRYLSAEUREESTER. VI: NOTIZ ZUR GAMMA -BROMIERUNG VON 2-ISOTHIOCYANATO-2-BUTENSAEUREESTERN UND ZUR NACHFOLGENDEN NUCLEOPHILEN SUBSTITUTION
- Other title
- ALPHA -ISOTHIOCYANATO ACRYLATES. VI. NOTE SUR LA GAMMA -BROMATION DES ISOTHIOCYANATO BUTENE-2 AORTES ET SUR LEURS SUBSTITUTIONS NUCLEOPHILES (fr)
- Author
- KLOFT M; HOPPE D
UNIV. GOETTINGEN, ORGAN.-CHEM. INST.,GOETTINGEN 3400,DEU - Source
- CHEM. BER.; DEU; DA. 1979; VOL. 112; NO 12; PP. 3939-3941; ABS. ENG; BIBL. 10 REF.
- Document type
- Article
- Language
- German
- Keyword (fr)
- REACTION CHIMIQUE NUCLEOPHILE ISOTHIOCYANATE ORGANIQUE COMPOSE VINYLIQUE COMPOSE ALIPHATIQUE CYCLOALKYLATION SUBSTITUTION HETEROCYCLE SOUFRE AZOTE CYCLE 6 CHAINONS COMPOSE ORGANIQUE BROME DITHIOCARBONIMIDATE ORGANIQUE COMPOSE BENZENIQUE BROMATION ACETIQUE ACIDE!ENT BUTENE-2OIQUE ACIDE(ISOTHIOCYANATO-2 PHENYL-3) ESTER ETHYLE!ENT BUTENE-2OIQUE ACIDE(ISOTHIOCYANATO-2 METHYL-3) ESTER ETHYLE!ENT THIAZINE-1,3CARBOXYLIQUE-4 ACIDE(BENZYLTHIO-2 PHENYL-5) ESTER ETHYLE!FIN BENZENETHIOL!ENT BUTENE-2OIQUE ACIDE(BROMO-4 ISOTHIOCYANATO-2 PHENYL-3) ESTER ETHYLE!FIN!ENT BUTENE-2OIQUE ACIDE(BROMO-4 BROMOMETHYL-3 ISOTHIOCYANATO) ESTER ETHYLE!FIN!ENT ALPHA -TOLUENETHIOL!ENT NBS!ENT CHIMIE ORGANIQUE
- Keyword (en)
- CHEMICAL REACTION NUCLEOPHILE ORGANIC ISOTHIOCYANATE VINYLIC COMPOUND ALIPHATIC COMPOUND CYCLOALKYLATION SUBSTITUTION SULFUR NITROGEN HETEROCYCLE SIX MEMBERED RING ORGANIC DITHIOCARBONIMIDATE BENZENIC COMPOUND BROMINATION ORGANIC CHEMISTRY
- Keyword (es)
- QUIMICA ORGANICA
- Classification
- Discipline
- General chemistry and physical chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- PASCAL8060269552
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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