Tetrahedron letters

A facile synthesis of tubercidin and related 7-deazapurine nucleosides via the stereospecific sodium salt glycosylation procedure

K Ramasamy, N Imamura, RK Robins, GR Revankar

Index: Ramasamy; Imamura; Robins; Revankar Tetrahedron Letters, 1987 , vol. 28, # 43 p. 5107 - 5110

Full Text: HTML

Citation Number: 37

Abstract

Summary. A facile high-yield synthesis of 7-deazaadenosine(tubercidin, z), 7- deazaguanosine (lo) t 2'-deoxy-7-deaza-6-thioguanosine(12) and 2'-deoxy-7- deazaguanosine(15) by the regioselective and stereospecific sodium salt glycosylation procedure is described.

Related Articles:

Structure− activity relationships of 7-deaza-6-benzylthioinosine analogues as ligands of Toxoplasma gondii adenosine kinase

[Journal of Medicinal Chemistry, , vol. 51, # 13 p. 3934 - 3945]

Stereoselective synthesis of pyrrolo [2, 3??d] pyrimidine α??and β??D??ribonucleosides from anomerically pure D??ribofuranosyl chlorides: Solid??Liquid Phase??Transfer …

[Helvetica Chimica Acta, , vol. 71, # 6 p. 1573 - 1585]

6-(Het) aryl-7-deazapurine ribonucleosides as novel potent cytostatic agents

[Journal of Medicinal Chemistry, , vol. 53, # 1 p. 460 - 470]

More Articles...