On the selectivity of deprotection of benzyl, mpm (4-methoxybenzyl) and dmpm (3,4-dimethoxybenzyl) protecting groups for hydroxy functions
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference27 articles.
1. Specific removal of o-methoxybenzyl protection by DDQ oxidation.
2. Protection of hydroxy groups by intramolecular oxidative formation of methoxybenzylidene acetals with DDQ
3. Kinetic acetalization for 1,2- and 1,3-diol protection by the reaction of p-methoxyphenylmethyl methyl ether with DDQ
4. DMPM (3,4-dimethoxybenzyl) protecting group for hydroxy function more readily removable than MPM (P-methoxybenzyl) protecting group by DDQ oxidation
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