4-Quinolylmethyl and 1-Naphthylmethyl as Benzyl-type Protecting Groups of Carboxylic Acids Removable by Homogeneous Palladium-Catalyzed Hydrogenolysis
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference20 articles.
1. Palladium-catalyzed nucleophilic substitution of napht hylmethyl and 1-naphthylethyl esters
2. Palladium-catalyzed substitution of esters of naphthylmethanols, 1-naphthylethanols, and analogues by sodium dimethyl malonate. Stereoselective synthesis from enantiomerically pure substrates
3. Asymmetric palladium-catalyzed nucleophilic substitution of racemic 1-naphthylethyl esters
4. DMF as a dimethylamine equivalent in the palladium-catalyzed nucleophilic substitution of naphthylmethyl and allyl acetates
5. Protective Groups in Organic Synthesis;Greene,1991
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1. 1-Naphthylmethyl and 1-naphthylmethoxymethyl protecting groups: New members of the benzyl- and benzyloxymethyl-type family;Tetrahedron Letters;2017-06
2. Protection for the Carboxyl Group;Greene's Protective Groups in Organic Synthesis;2014-08-11
3. Pd0-Catalyzed Hydrogenolysis of a Bicyclic Allylic Diacetate;European Journal of Organic Chemistry;2013-08-15
4. ChemInform Abstract: 4-Quinolylmethyl and 1-Naphthylmethyl as Benzyl-Type Protecting Groups of Carboxylic Acids Removable by Homogeneous Palladium-Catalyzed Hydrogenolysis.;ChemInform;2010-06-07
5. Catalytic Transformations of Benzylic Carboxylates and Carbonates;Synthesis;2009-03-06
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