First Evident Generation of Purin-2-yllithium: Lithiation of an 8-Silyl-Protected 6-Chloropurine Riboside as a Key Step for the Synthesis of 2-Carbon-Substituted Adenosines
- 28 September 1999
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 64 (21) , 7773-7780
- https://doi.org/10.1021/jo9906577
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Adenosine receptor agonists: Synthesis and biological evaluation of the diastereoisomers of 2-(3-hydroxy-3-phenyl-1-propyn-1-yl)NECABioorganic & Medicinal Chemistry, 1997
- A New Entry to 2-Substituted Purine Nucleosides Based on Lithiation-Mediated Stannyl Transfer of 6-Chloropurine NucleosidesThe Journal of Organic Chemistry, 1997
- Nucleosides and nucleotides. 103. 2-Alkynyladenosines: a novel class of selective adenosine A2 receptor agonists with potent antihypertensive effectsJournal of Medicinal Chemistry, 1992
- Principles of Nucleic Acid StructurePublished by Springer Nature ,1984
- “Umpulong” of reactivity at the C-6 position of uridine: a simple and general method for 6-substituted uridinesTetrahedron, 1982
- Studies on chemical alterations of nucleic acids and their components—VIITetrahedron, 1974
- Synthesis of 2-methyladenosine and its 5'-phosphateThe Journal of Organic Chemistry, 1968
- Antituberculous Compounds. XXII.1 MonoalkylaminobenzothioamidesJournal of Medicinal Chemistry, 1965
- Some Synthetic Analogs of the Natural Purine Nucleosides1Journal of the American Chemical Society, 1952