Chun, MW Kim, MJ Jo, UH Kim, JH Kim, HD Jeong, LS 2024-01-21T12:42:19Z 2024-01-21T12:42:19Z 2021-09-04 2001-03 1525-7770 https://pubs.kist.re.kr/handle/201004/140694 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. English MARCEL DEKKER INC OXETANOCIN Synthesis of novel 3 '-deoxy-3 '-C-hydroxymethyl nucleosides with conformationally rigid sugar moiety as potential antiviral agents Article 10.1081/NCN-100002354 1 NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS, v.20, no.4-7, pp.699 - 702 NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS 20 4-7 699 702 scie scopus 000170690500057 2-s2.0-0034851894 Biochemistry & Molecular Biology Biochemistry & Molecular Biology Article; Proceedings Paper OXETANOCIN synthesis