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TRIMETHYLSILYLCYANID ALS UMPOLUNGSREAGENS. VII: NUCLEOPHILE ACYLIERUNG VON CARBONYLVERBINDUNGEN MIT ALPHA ,BETA -UNGESAETTIGTEN ALDEHYDEN

Other title
LE CYANURE DE TRIMETHYLSILYLE COMME REACTIF D'INVERSION DE POLARITE. VII. ACYLATION NUCLEOPHILE DE COMPOSES CARBONYLES AVEC DES ALDEHYDES ALPHA ,BETA -INSATURES (fr)
Author
HUENIG S; OELLER M
UNIV. WUERZBURG, INST. ORGAN. CHEM./WUERZBURG 8700/DEU
Source
CHEM. BER.; ISSN 0009-2940; DEU; DA. 1981; VOL. 114; NO 3; PP. 959-967; ABS. ENG; BIBL. 19 REF.
Document type
Article
Language
German
Keyword (fr)
CARBANION SILICIUM COMPOSE ORGANIQUE REACTION NUCLEOPHILE CYANHYDRINE ENONE COMPOSE VINYLIQUE COMPOSE ALIPHATIQUE INVERSION POLARITE COMPOSE MONOCYCLIQUE TRANSPOSITION COMPOSE SATURE CETOESTER COMPOSE ETHYLENIQUE ADDITION MICHAEL ACYLATION ACETONE!ENT BUTENE-2URE-1(CYANO-1 TRIMETHYLSILOXY-1)!FIN!ENT ACETOPHENONE!ENT CYCLOHEXANONE(T-BUTYL-4)!ENT FORMALDEHYDE!ENT PROPANAL(DIMETHYL-2,2)!ENT PENTENE-3ONE-2(METHYL-4)!ENT ACRYLIQUE ACIDE,ESTER ETHYLE!ENT CINNAMIQUE ACIDE,ESTER ETHYLE!ENT ACROLEINE!ENT CYCLOPENTADIENE!ENT HEPTENE-5OIQUE ACIDE(METHYL-6 OXO-4) ESTER ETHYLE!FIN CYCLOPROPANECARBOXYLIQUE ACIDE(METHYL-1 METHYL-3 BUTENE-2P OYL-2) ESTER ETHYLE!FIN LITHIUM AMIDURE(DIISOPROPYL)!ENT THF!SUB CHIMIE ORGANIQUE
Keyword (en)
CARBANION NUCLEOPHILIC REACTION CYANOHYDRIN ENONE VINYLIC COMPOUND ALIPHATIC COMPOUND POLARITY INVERSION MONOCYCLIC COMPOUND TRANSPOSITION SATURATED COMPOUND KETOESTER ETHYLENIC COMPOUND MICHAEL ADDITION ACYLATION 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
PASCAL8130302624

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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