Diimidazo [1, 2-c: 4′, 5′-e] pyrimidines: N 6-N1 conformationally restricted adenosines

D Camp, Y Li, A McCluskey, RW Moni…

Index: Camp, David; Li, Ying; McCluskey, Adam; Moni, Roger W.; Quinn, Ronald J. Bioorganic and Medicinal Chemistry Letters, 1998 , vol. 8, # 6 p. 695 - 698

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Citation Number: 5

Abstract

Download full text in PDF Opens in a new window. Article suggestions will be shown in a dialog on return to ScienceDirect. ... Please enable JavaScript to use all the features on this page. ... Tethering the N 6 -substituents of N 6 -substituted adenosines to N1 has resulted in a series of conformationally restricted adenosine analogues. The resultant diimidazo[1,2-c:4′,5′-e] pyrimidines were shown to be adenosine A 1 selective. ... Tethering the N 6 -substituents ...