Paper
Protection of Alcohols Using 2‐Benzyloxy‐1‐Methylpyridinium Trifluoromethanesulfonate: Methyl (R)‐(−)‐3‐Benzyloxy‐2‐Methyl Propanote
Published Oct 15, 2007 · Kevin W. C. Poon, Philip A. Albiniak, G. Dudley
Organic Syntheses
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Abstract
Benzyl alcohol 2-Chloropyridine 2-Benzyloxypyridine 2-Benzyloxy-1-methylpyridinium trifluoromethanesulfonate Methyl (R)-(−)-3-benzyloxy-2-methyl propanoate Magnesium oxide Methyl (R)-(−)-3-hydroxy-2-methyl propionate Keywords: alcohol protection; benzylation reactions; benzyl ethers; Williamson ether synthesis; coupling; trifluoromethanesulfonic acid; benzyloxymethylpyridinium triflate; waste disposal
Using 2Benzyloxy-1Methylpyridinium Trifluoromethanesulfonate effectively protects alcohols from waste disposal and benzylation reactions.
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