Radical-chain deoxygenation of tertiary alcohols, protected as their methoxymethyl (MOM) ethers, using thiols as polarity- reversal catalysts.
499 - 500.
The deoxygenation of tertiary alcohols can be accomplished by heating their MOM ethers in the presence of a peroxide initiator and a thiol catalyst: the proposed radical-chain mechanism is supported by EPR spectroscopic studies
|Title:||Radical-chain deoxygenation of tertiary alcohols, protected as their methoxymethyl (MOM) ethers, using thiols as polarity- reversal catalysts|
|Additional information:||Journal Article 292YA Roberts BP Univ London Univ Coll, Dept Chem, Christopher Ingold Labs, 20 Gordon St, London WC1H 0AJ, England CHEM COMMUN|
|Keywords:||Alcohol, ALCOHOLS, As, CATALYSTS, ELECTRON-SPIN RESONANCE, EPR, MECHANISM, thiols|
|UCL classification:||UCL > School of BEAMS > Faculty of Maths and Physical Sciences > Chemistry|
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