Preparation of 8-Chloropurine Nucleosides Through the Reaction Between their C-8 Lithiated Species andp-Toluenesulfonyl Chloride
Author:
Publisher
Informa UK Limited
Subject
Genetics,Biochemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/07328318808068708
Reference8 articles.
1. Preparation of 8-chloroadenosine and its phosphate esters
2. Intestinal absorption aspect of non-lipophilic low molecular weight drugs: A case of cephalexin and cefazolin.
3. New procedure for the chlorination of pyrimidine and purine nucleosides
4. Direct C-8 lithiation of naturally-occurring purine nucleosides. A simple method for the synthesis of 8-carbon-substituted purine nucleosides.
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1. Efficient functionalization of 2-amino-6-chloropurine derivatives at C-8 via 8-lithiated species;Tetrahedron Letters;2015-10
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3. Halogen–deuterium exchange reaction mediated by tributyltin hydride using THF-d8 as the deuterium source;Tetrahedron;2011-02
4. Alternative I-D Exchange Reaction on Pyrimidine and Purine Nuclei Mediated by Tributyltin Hydride Using THF-d 8 as a Deuterium Source;Synlett;2008-10-15
5. Structural Determinants for N1/N7 Cyclization of Nicotinamide Hypoxanthine 5‘-Dinucleotide (NHD+) Derivatives by ADP-Ribosyl Cyclase from Aplysia californica: Ca2+-Mobilizing Activity of 8-Substituted Cyclic Inosine 5‘-Diphosphoribose Analogues in T-Lymphocytes;Journal of Medicinal Chemistry;2006-07-28
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