The synthesis of 4-amino-8-(β--ribofuranosyl)aminopyrimido[5,4-]pyrimidine from a purine nucleoside: a novel rearrangement of the purine ring
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference9 articles.
1. Non-catalytic Fusion Reaction of 1, 2, 3, 5-Tetra-O-acetyl-β-D-ribofuranose with Purine Derivatives
2. Catalysts and By-products in the Fusion Reaction of Acetylated Sugars with Purine Derivatives
3. Purine studies. Part I. Stability to acid and alkali. Solubility. Ionization. Comparison with pteridines
4. A Study of the Action of Acid and Alkali on Certain Purines and Purine Nucleosides1
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1. Applications of Purine Ring Opening in the Synthesis of Imidazole, Pyrimidine, and New Purine Derivatives;European Journal of Organic Chemistry;2021-08-26
2. Bicyclic 6 + 6 systems: the chemistry of pyrimido[4,5-d]pyrimidines and pyrimido[5,4-d]pyrimidines;RSC Advances;2019
3. Dimroth-type rearrangement of 1-benzyl- and 1-glycosyl-5-aminoimidazoles to 4-(N-substituted amino)imidazoles;Tetrahedron Letters;2012-01
4. Synthesis and in vitro evaluation of substituted pyrimido[5,4-d]pyrimidines as a novel class of Antimycobacterium tuberculosis agents;European Journal of Medicinal Chemistry;2010-07
5. A Mild Approach to the Synthesis of 4-Amino-8-(arylamino)pyrimido[5,4-d]pyrimidine 3-Oxides;European Journal of Organic Chemistry;2009-10
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