Nucleosides, Nucleotides and Nucleic Acids vol. 22, no. 5-8, pp. 919 - 921
Indexed
SCIE; SCOPUS
Document Type
Conference Paper
Abstract
Novel halovinyl analogues of neplanocin A without 4′-hydroxymethyl group were easily synthesized starting from D-ribose via cyclopentenone 5 as a key intermediate and their inhibitory activity against SAH hydrolase was assayed.