A Useful Methodology for the Regioselective Deprotection of 1,3-Dibenzyluracils
- 1 November 1991
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 21 (21) , 2181-2187
- https://doi.org/10.1080/00397919108055451
Abstract
A practical, regioselective N-1 deprotection of 1,3-dibenzyl uracils 2 a-e is described. The same experimental procedure and longer reaction time afforded the complete deprotection of the uracils.Keywords
This publication has 9 references indexed in Scilit:
- 6-alkyl and 5,6-dialkyl-2-methoxy-4(3H)- pyrimidinones in the transformations of pyrimidines—2Tetrahedron, 1984
- Removal of n-benzyl-and n-benzyloxymethyl substituents from substituted uracils with boron tribromideTetrahedron Letters, 1980
- Reactions of arylsulfonylacetylenes with organolithium and Grignard reagents: a new synthesis of acetylenesThe Journal of Organic Chemistry, 1979
- Facile alkylation of purines, pyrimidines, nucleosides and nucleotides using tetrabutylammonium fluorideTetrahedron Letters, 1978
- Rapid removal of protecting groups from peptides by catalytic transfer hydrogenation with 1,4-cyclohexadieneThe Journal of Organic Chemistry, 1978
- Transfer hydrogenation; a convenient method for removal of some commonly used protecting groups in peptide synthesisJournal of the Chemical Society, Perkin Transactions 1, 1977
- Nucleosides. XVII. Benzylation-debenzylation studies on nucleosidesThe Journal of Organic Chemistry, 1975
- 5-Amino-4-imidazolecarboxamide Riboside from Inosine. Ring-opening Reactions of Purine NucleosidesJournal of the American Chemical Society, 1958