Moon, HR Kim, HO Lee, KM Chun, MW Kim, JH Jeong, LS 2024-01-21T10:01:30Z 2024-01-21T10:01:30Z 2021-09-01 2002-10-03 1523-7060 https://pubs.kist.re.kr/handle/201004/139137 [GRAPHICS] A total synthesis of apio-neplanocin A, which combines properties of apio nucleoside and neplanocin A and is a potential inhibitor of S-adenosylhomocysteine hydrolase, was accomplished starting from D-ribose via stereoselective hydroxymethylation and RCM reaction. English AMER CHEMICAL SOC CARBOCYCLIC ADENOSINE-ANALOGS 2&apos -DEOXY-3&apos -THIACYTIDINE BCH-189 ANTIVIRAL ACTIVITY L929 CELLS MECHANISM SPECTRUM INVITRO TARGET AGENTS Stereoselective synthesis of a novel apio analogue of neplanocin A as potential S-adenosylhomocysteine hydrolase inhibitor Article 10.1021/ol026624m 1 ORGANIC LETTERS, v.4, no.20, pp.3501 - 3503 ORGANIC LETTERS 4 20 3501 3503 scie scopus 000178327500042 2-s2.0-0037015428 Chemistry, Organic Chemistry Article CARBOCYCLIC ADENOSINE-ANALOGS 2&apos -DEOXY-3&apos -THIACYTIDINE BCH-189 ANTIVIRAL ACTIVITY L929 CELLS MECHANISM SPECTRUM INVITRO TARGET AGENTS synthesis