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A NOVEL METHOD FOR THE ALPHA -PHENYLTHIOMETHYLATION OF CARBONYL COMPOUNDS

Author
SUZUKI K; SEKIYA M
SHIZUOKA COLL. PHARM./SHIZUOKA-SHI 422/JPN
Source
SYNTHESIS (STUTTG.); ISSN 0039-7881; DEU; DA. 1981; NO 4; PP. 297-299; BIBL. 7 REF.
Document type
Article
Language
English
Keyword (fr)
ALDEHYDE REACTION CHIMIQUE PREPARATION ENAMINE THIOHEMIAMINAL HYDROGENE CHLORURE!ACT AMINE TERTIAIRE HETEROCYCLE OXYGENE AZOTE CYCLE 6 CHAINONS COMPOSE MONOCYCLIQUE COMPOSE SATURE CETOSULFURE COMPOSE BENZENIQUE EFFET STRUCTURE ALKYLATION CETONE ETHANOL!SUB AMINE(CYCLOHEXENE-1YL DIMETHYL)!FIN!ENT MORPHOLINE(CYCLOHEXENE-1P YL-4)!FIN!ENT CYCLOHEXANONE(PHENYLTHIOMETHYL-2)!FIN CYCLOHEXANONE(ALKYLTHIOMETHYL-2)!FIN BUTANAL(PHENYLTHIOMETHYL-2)!FIN NONANONE-5(PHENYLTHIOMETHYL-4)!FIN PROPIOPHENONE(PHENYLTHIO-3)!FIN BORNANONE-2(PHENYLTHIOMETHYL-3)!FIN PENTANONE-3(METHYL-4 PHENYLTHIO-1)!FIN METHANE(DIMETHYLAMINO METHYLTHIO)!ENT METHANE(DIMETHYLAMINO PHENYLTHIO)!ENT SUBSTITUTION ELECTROPHILE ALDEHYDOSULFURE COMPOSE ALIPHATIQUE COMPOSE BICYCLIQUE ALKYLTHIOALKYLATION CHIMIE ORGANIQUE
Keyword (en)
ALDEHYDE CHEMICAL REACTION PREPARATION ENAMINE THIOHEMIAMINAL TERTIARY AMINE OXYGEN NITROGEN HETEROCYCLE SIX MEMBERED RING MONOCYCLIC COMPOUND SATURATED COMPOUND KETOSULFIDE BENZENIC COMPOUND STRUCTURE EFFECT ALKYLATION KETONE ELECTROPHILIC SUBSTITUTION ALDEHYDOSULFIDE ALIPHATIC COMPOUND BICYCLIC COMPOUND 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
PASCAL8130346441

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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