Protection of Alcohols Using 2‐Benzyloxy‐1‐Methylpyridinium Trifluoromethanesulfonate: Methyl ( <scp>R</scp> )‐(−)‐3‐Benzyloxy‐2‐Methyl Propanote
説明
<jats:title>Abstract</jats:title> <jats:p> <jats:list list-type="simple"> <jats:list-item> <jats:p>Benzyl alcohol</jats:p> </jats:list-item> <jats:list-item> <jats:p>2‐Chloropyridine</jats:p> </jats:list-item> <jats:list-item> <jats:p>2‐Benzyloxypyridine</jats:p> </jats:list-item> <jats:list-item> <jats:p>2‐Benzyloxy‐1‐methylpyridinium trifluoromethanesulfonate</jats:p> </jats:list-item> <jats:list-item> <jats:p>Methyl (R)‐(−)‐3‐benzyloxy‐2‐methyl propanoate</jats:p> </jats:list-item> <jats:list-item> <jats:p>Magnesium oxide</jats:p> </jats:list-item> <jats:list-item> <jats:p>Methyl (R)‐(−)‐3‐hydroxy‐2‐methyl propionate</jats:p> </jats:list-item> </jats:list> </jats:p>
収録刊行物
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- Organic Syntheses
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Organic Syntheses 295-305, 2007-09-11
Wiley