142095-47-4Relevant articles and documents
The synthesis of two 2'-deoxy carbocyclic purine nucleosides lacking the 5'-methylene
Koga,Schneller
, p. 5861 - 5864 (1990)
The synthesis of the adenine derivative (±)-(1α,2β,4α)-4-(6-amino-9H-purin-9-yl)-1,2-cyclopentanediol (2) and its hypoxanthine analogue (3) as carbocyclic nucleosides lacking the 5'-methylene is described in 7 steps from 3-cyclopenten-1-ylamine hydrochlor
(+/-)-Carbocyclic 5'-Nor-2'-deoxyguanosine and Related Purine Derivatives: Synthesis and Antiviral Properties
Patil, Sharadbala D.,Koga, Masakazu,Schneller, Stewart W.,Snoeck, Robert,Clercq, Erik De
, p. 2191 - 2195 (2007/10/02)
Beginning with 3-cyclopenten-1-ylamine hydrochloride, the 5'-nor derivatives of carbocyclic 2'-deoxyguanosine (2), 2'-deoxyadenosine (3),, and 2,6-diaminopurine 2'-deoxyribofuranoside (4) have been prepared.These compounds were evaluated for antiviral pot