Application of the Benzyloxycarbonyloxymethyl Moiety to a Protective Group of 5-Fluorouracil. Selective Alkylation of Amide Nitrogen of the Uracil Ring
- 5 August 1988
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 17 (8) , 1381-1384
- https://doi.org/10.1246/cl.1988.1381
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- Selective Synthesis of 1-Alkoxycarbonyloxymethyl-5-fluorouracils via 1,3-Bis(hydroxymethyl)-5-fluorouracilHETEROCYCLES, 1988
- A facile method for synthesis of N-acyloxymethyl-5-fluorouracils, as a class of antitumor agents.CHEMICAL & PHARMACEUTICAL BULLETIN, 1986
- Removal of n-benzyl-and n-benzyloxymethyl substituents from substituted uracils with boron tribromideTetrahedron Letters, 1980
- Studies on the syntheses of heterocyclic compounds. 845. Studies on the synthesis of chemotherapeutics. 10. Synthesis and antitumor activity of N-acyl- and N-(alkoxycarbonyl)-5-fluorouracil derivativesJournal of Medicinal Chemistry, 1980
- Synthesis of 3-(Tetrahydro-2-furanyl)-5-fluorouracilYAKUGAKU ZASSHI, 1978