ALPHA -METHYLENATION OF LACTONES AND ESTERS ZINC BROMIDE-CATALYSED PHENYLTHIOMETHYLATION OF O-SILYLATED ENOLATES
- Author
- PATERSON I; FLEMING I
UNIV. CHEM. LAB., CAMBRIDGE CB2 1EW, GBR - Source
- TETRAHEDRON LETTERS; GBR; DA. 1979; NO 11; PP. 993-994; BIBL. 9 REF.
- Document type
- Article
- Language
- English
- Keyword (fr)
- HETEROCYCLE OXYGENE LACTONE CYCLE 6 CHAINONS SILICIUM COMPOSE ORGANIQUE ENOL ETHER PREPARATION REACTION CATALYTIQUE SILYLATION ZINC II BROMURE!ACT OXYDATION PYROLYSE ESTER COMPOSE ALIPHATIQUE ALKYLIDENATION SODIUM PERIODATE!ENT SILANE(CHLORO TRIMETHYL)!ENT BENZOFURANNONE-2(PERHYDRO)!ENT PYRANNONE-2(PERHYDRO)!ENT SULFURE(CHLOROMETHYL PHENYL)!ENT BUTYRIQUE ACIDE,ESTER ETHYLE!ENT ACRYLIQUE ACIDE(ETHYL-2) ESTER ETHYLE!FIN SILANE(ETHOXY-1 BUTENE-1YLOXY TRIMETHYL)!FIN!ENT BUTYRIQUE ACIDE(PHENYLTHIOMETHYL-2) ESTER ETHYLE!FIN!ENT PYRANNE(DIHYDRO-3,4 TRIMETHYLSILOXY-6)!FIN!ENT PYRANNONE-2(PERHYDRO PHENYLTHIOMETHYL-3)!FIN!ENT PYRANNONE-2(METHYLENE-3 PERHYDRO)!FIN BENZOFURANNONE-2(METHYLENE-3 PERHYDRO)!FIN ACETIQUE ACIDE!SUB METHANOL!SUB COMPOSE SATURE CETENE DERIVE ACETAL BENZOFURANNONE-2(PERHYDRO PHENYLTHIOMETHYL-3)!FIN!ENT COMPOSE BICYCLIQUE BENZOFURANNE(HEXAHYDRO TRIMETHYLSILOXY-2)!FIN!ENT CHIMIE ORGANIQUE
- Keyword (en)
- OXYGEN HETEROCYCLE LACTONE SIX MEMBERED RING ENOL ETHER PREPARATION CATALYTIC REACTION SILYLATION OXIDATION PYROLYSIS ESTER ALIPHATIC COMPOUND ALKYLIDENATION SATURATED COMPOUND ACETAL BICYCLIC COMPOUND ORGANIC CHEMISTRY
- Keyword (es)
- QUIMICA ORGANICA
- Classification
- Discipline
- General chemistry and physical chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- PASCAL7960332616
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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