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TRIMETHYLSILYLCYANID ALS UMPOLUNGSREAGENS. III: NUCLEOPHILE ACYLIERUNG VON ALPHA ,BETA -UNGESAETTIGTEN CARBONYLVERBINDUNGEN UNTER STEUERUNG DER 1,2-/1,4-ADDITION DURCH SOLVENSEFFEKTE

Other title
LE CYANURE DE TRIMETHYLSILYLE COMME AGENT D'INVERSION DE POLARITE. III: ACYLATION NUCLEOPHILE DE COMPOSES CARBONYLES ALPHA ,BETA -INSATURES AVEC DIRECTION DES ADDITIONS-1,2/-1,4 PAR DES EFFETS DE SOLVANT (fr)
Author
HUENIG S; WEHNER G
UNIV. WUERZBURG, INST. ORGAN. CHEM.,WUERZBURG 8700,DEU
Source
CHEM. BER.; DEU; DA. 1980; VOL. 113; NO 1; PP. 302-323; ABS. ENG; BIBL. 62 REF.
Document type
Article
Language
German
Keyword (fr)
SILICIUM COMPOSE ORGANIQUE ACYLATION REACTION NUCLEOPHILE EFFET SOLVANT CARBANION COMPOSE ALIPHATIQUE COMPOSE MONOCYCLIQUE DICETONE ORIENTATION REACTION PAIRE ION ADDITION ENONE BENZENEACETONITRILE(ALPHA -TRIMETHYLSILOXY)!ENT PENTENE-3ONE-2(METHYL-4)!ENT BUTENE-3ONE-2(PHENYL-4)!ENT CYCLOHEXENE-2ONE(METHYL-5)!ENT CYCLOHEXENE-2ONE(TRIMETHYL-3,5,5)!ENT NAPHTALENONE-2(OCTAHYDRO-2,3,4,4A,5,6,7,8)!ENT BENZENEACETONITRILE(ALPHA -LITHIO ALPHA -TRIMETHYLSILOXY)!FIN!ENT CYCLOHEXANONE(BENZOYL-3)!FIN BENZOIQUE ACIDE,CHLORURE!ENT CINNAMIQUE ACIDE,ESTER METHYLE!ENT BUTENE-2OIQUE ACIDE(METHYL-3) ESTER METHYLE!ENT SILANE(CYANO TRIMETHYL) LITHIUM AMIDURE(DIISOPROPYL)!ENT ETHYLE ETHER!SUB THF!SUB MONOGLYME!SUB HMPT!ACT 12-CROWN-4!ACT CHIMIE ORGANIQUE
Keyword (en)
ACYLATION NUCLEOPHILIC REACTION SOLVENT EFFECT CARBANION ALIPHATIC COMPOUND MONOCYCLIC COMPOUND DIKETONE REACTION ORIENTATION ION PAIR ADDITION ENONE ORGANIC CHEMISTRY
Keyword (es)
QUIMICA ORGANICA
Classification
Pascal
001 Exact sciences and technology / 001C Chemistry / 001C01 General and physical chemistry

Discipline
General chemistry and physical chemistry
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
PASCAL8060313680

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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