Ring Cleavage and Modification at C-2 of a 3,5′-Cyclonucleoside Derivative of Adenosine
- 1 February 1976
- journal article
- research article
- Published by Oxford University Press (OUP) in Agricultural and Biological Chemistry
- Vol. 40 (2) , 373-376
- https://doi.org/10.1080/00021369.1976.10862039
Abstract
It was shown that under alkaline conditions the cyclonucleoside 1 was converted to an imidazole cyclonucleoside 2, and under milder conditions it was converted to an amidine 3, which reacted with N,N′-thiocarbonyldiimidazole and cyanogen bromide as well as phosgene affording the corresponding ring closure products 8, 9 and 10.This publication has 0 references indexed in Scilit: