A highly efficient method for the reductive etherification of carbonyl compounds with triethylsilane and alkoxytrimethylsilane catalyzed by iron(III) chloride

Synthesis

Volumn , Issue 2, 2005, Pages 183-186

  Iwanami, Katsuyuki ^a   Seo, Hana ^a   Tobita, Yuki ^a   Oriyama, Takeshi ^a  

^a IBARAKI UNIVERSITY   (Japan)

Author keywords

Alkoxytrimethylsilane; Carbonyl compounds; Iron(III) chloride; Reductive etherification; Triethylsilane

Indexed keywords

ALCOHOLS; BENZENE; CATALYSIS; ETHERS; IRON COMPOUNDS; REACTION KINETICS; REDUCTION; SILANES;

ALKYL ETHERS; CARBONYL COMPOUNDS; REACTION CONDITIONS; REDUCTIVE ETHERIFICATION;

SYNTHESIS (CHEMICAL);

ALCOHOL DERIVATIVE; ALDEHYDE; ALKYL ETHER; ALLYL ETHER; BENZYL 3 PHENYLPROPYL ETHER; BENZYL ETHER; BENZYLOXYTRIMETHYLSILANE; CARBONYL DERIVATIVE; ETHER DERIVATIVE; FERRIC CHLORIDE; HYDROCINNAMALDEHYDE; KETONE; NITROMETHANE; SILANE DERIVATIVE; TRIETHYLSILANE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CATALYST; ETHERIFICATION; INFRARED SPECTROSCOPY; PROTON NUCLEAR MAGNETIC RESONANCE; REDUCTION; SYNTHESIS; THIN LAYER CHROMATOGRAPHY;

EID: 13844289128     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2004-834942     Document Type: Article

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