Preferential hydrogenolysis of NAP esters provides a new orthogonal protecting group strategy for carboxylic acids
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference9 articles.
1. Protective Groups in Organic Synthesis;Greene,1991
2. Protecting Groups;Kocienski,1994
3. Rational Design of Benzyl-Type Protecting Groups Allows Sequential Deprotection of Hydroxyl Groups by Catalytic Hydrogenolysis
4. The total syntheses of the isodityrosine-derived cyclic tripeptides OF4949-III and K-13. Determination of the absolute configuration of K-13
5. Deprotection of carboxylic esters of .beta.-lactam homologs. Cleavage of p-methoxybenzyl, diphenylmethyl, and tert-butyl esters effected by a phenolic matrix
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1. New aziridine-based inhibitors of cathepsin L-like cysteine proteases with selectivity for the Leishmania cysteine protease LmCPB2.8;European Journal of Medicinal Chemistry;2018-08
2. Protection for the Carboxyl Group;Greene's Protective Groups in Organic Synthesis;2014-08-11
3. Palladium/Carbon;Fieser and Fieser's Reagents for Organic Synthesis;2013-04-26
4. Selective removal of the (2-naphthyl)methyl protecting group in the presence of p-methoxybenzyl group by catalytic hydrogenation;Arkivoc;2012-06-22
5. Palladium/Carbon;Fieser and Fieser's Reagents for Organic Synthesis;2011-08-15
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