161987-82-2Relevant articles and documents
Synthesis and biological evaluation of pyrimidine nucleosides fused with 3′,4′-tetrahydrofuran ring
Chun, Moon Woo,Kim, Myong Jung,Kim, Hea Ok,Moon, Hyung Ryong,Kim, Hee-Doo,Kim, Joong Hyup,Jeong, Lak Shin
, p. 719 - 721 (2007/10/03)
Pyrimidine nucleosides fused with 3′,4′-tetrahydrofuran ring were synthesized, starting from 1,2;5,6-di-O-isopropylidene-D-glucose and assayed for antiviral activities. Thymine analogue 1 and its corresponding 2′-deoxy analogue 3 exhibited high cytotoxici
Synthesis of novel 3′-deoxy-3′-C-hydroxymethyl nucleosides with conformationally rigid sugar moiety as potential antiviral agents
Moon Woo Chun,Myung Jung Kim,Un Hee Jo,Joong Hyup Kim,Kim,Lak Shin Jeong
, p. 699 - 702 (2007/10/03)
Based on the fact that the ring expanded 3′-C-hydroxymethyl analogue of oxetanocin A exhibited potent antiviral activity, two types of conformationally rigid 3′-C-hydroxymethyl derivatives in which 2′-hydroxyl group is linked to the 4′-position or to the 6′-position were synthesized starting from 1,2;5,6-di-O-isopropylidene-D-glucose, respectively.