COMPLETE DIASTEREOFACE SELECTION IN THE LEWIS ACID-MEDIATED ALDOL REACTIONS OF C,O-DISILYLATED GAMMA -BUTYROLACTONE ENOLATES WITH ALDEHYDES
- Author
- YAMAMOTO K; TOMO Y
TOKYO INST. TECHNOLOGY/TOKYO 152/JPN - Source
- CHEMISTRY LETTERS; ISSN 0366-7022; JPN; DA. 1983; NO 4; PP. 531-534; BIBL. 10 REF.
- Document type
- Article
- Language
- English
- Keyword (fr)
- ALDOLISATION CATALYSE ACIDE ACIDE LEWIS TITANE IV CHLORURE!ACT ACETAL ENOLATE HETEROCYCLE OXYGENE CYCLE 5 CHAINONS LACTONE DIASTEREOSELECTIVITE SILICIUM COMPOSE ORGANIQUE ETAT TRANSITION CYCLE 6 CHAINONS FURANNE(DIHYDRO-4,5 METHYL-5 TRIMETHYLSILOXY-2 TRIMETHYLSILYL-3)!ENT ACETALDEHYDE!ENT FURANNONE-2(HYDROXY-1P ETHYL-2 METHYL-5 PERHYDRO TRIMETHYLSILYL-3)!FIN PYRANNE DERIVE!ENT CHIMIE ORGANIQUE
- Keyword (en)
- ALDOL CONDENSATION ACID CATALYSIS LEWIS ACID TITANIUM IV CHLORIDES!ACT ACETAL ENOLATE OXYGEN HETEROCYCLE FIVE MEMBERED RING LACTONE DIASTEREOSELECTIVITY SILICON ORGANIC COMPOUNDS TRANSITION STATE SIX MEMBERED RING ORGANIC CHEMISTRY
- Keyword (es)
- QUIMICA ORGANICA
- Classification
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- PASCAL83X0403112
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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