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MODIFIZIERTE WICHTERLE-REAKTION. EIN WEG ZUR DARSTELLUNG VON 2-CYCLOHEXENONEN UND 1,4-DIKETONEN. SYNTHESE VON 4-ESTREN-3,17-DION UND DIHYDROJASMON

Other title
REACTION DE WICHTERLE MODIFIEE. UNE VOIE DE PREPARATION DE CYCLOHEXENE-2ONES ET DE DICETONES-1,4. SYNTHESE DE L'OESTRENE-4DIONE-3,17 ET DE LA DIHYDROJASMONE (fr)
Author
KOBAYASHI M; MATSUMOTO T
HOKKAIDO UNIV., DEP. CHEM.,SAPPORO 060,JPN
Source
BULL. CHEM. SOC. JAP.; JPN; DA. 1979; VOL. 52; NO 10; PP. 2978-2990; BIBL. 41 REF.
Document type
Article
Language
German
Keyword (fr)
CYCLISATION EFFET SOLVANT PERCHLORIQUE ACIDE!ACT COMPOSE ALIPHATIQUE COMPOSE MONOCYCLIQUE COMPOSE BICYCLIQUE HALOGENOCETONE ENONE DICETONE STEROIDE MONOTERPENE CETOACIDE REACTION WICHTERLE CYCLOHEXANONE(CHLORO-3P BUTENE-2P YL-2 METHYL-2)!ENT BICYCLO (3.3.1) NONENE-2ONE-9(DIMETHYL-2,5)!FIN NAPHTALENONE-2(METHYL-4A OCTAHYDRO-2,3,4,4A,5,6,7,8)!FIN HEPTENE-5ONE-2(CHLORO-6)!ENT CYCLOHEXENE-2ONE(CHLORO-3P BUTENE-2P YL-2 METHYL-3)!ENT CYCLOPENTANEDIONE-1,3(CHLORO-3P BUTENE-2P YL-2 METHYL-2)!ENT CYCLOHEXANEDIONE-1,3(CHLORO-3P BUTENE-2P YL-2 TRIMETHYL-2,5,5)!ENT OESTRENE-4DIONE-3,17!FIN JASMONE(DIHYDRO-2P,3P)!FIN FORMIQUE ACIDE!ENT DECENE-8OIQUE ACIDE(CHLORO-9 OXO-5)!ENT CHIMIE ORGANIQUE
Keyword (en)
CYCLIZATION SOLVENT EFFECT ALIPHATIC COMPOUND MONOCYCLIC COMPOUND BICYCLIC COMPOUND HALOKETONE ENONE DIKETONE STEROID MONOTERPENE KETOACID WICHTERLE REACTION 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
PASCAL8060272033

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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