144534-61-2Relevant articles and documents
Synthesis of three new carbocyclic analogues of 3'-deoxy purine ribonucleosides
Agrofoglio,Condom,Guedj,Challand,Selway
, p. 1147 - 1160 (1994)
The 1-hydroxymethyl-3-cyclopentene (4) was converted, after epoxidation, to two new exocyclic amino carbocyclic nucleosides (1, 2), and a new cyclopentane nucleoside analogue (3), with potential biological activities. The regioselectivity of the epoxidation (4), which is the key step, is governed by steric control using aryl and silyl hydroxyl protecting groups.