Sequential removal of the benzyl-type protecting groups PMB and NAP by oxidative cleavage using CAN and DDQ
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference10 articles.
1. Rational Design of Benzyl-Type Protecting Groups Allows Sequential Deprotection of Hydroxyl Groups by Catalytic Hydrogenolysis
2. Preferential hydrogenolysis of NAP esters provides a new orthogonal protecting group strategy for carboxylic acids
3. Selective Hydrogenolysis of Novel Benzyl Carbamate Protecting Groups
4. Specific removal of o-methoxybenzyl protection by DDQ oxidation.
5. Use of 1,2-dichloro 4,5-dicyanoquinone (DDQ) for cleavage of the 2-naphthylmethyl (NAP) group
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