Syntheses and antiviral activities of 1,3-dioxolanyl-, 1,3-oxathiolanyl- and 1,3-dithiolanylnucleosides with 2-hydroxymethyl substituents

Authors
Chun, MWShin, DHMoon, HRLee, JWPark, HJeong, LS
Issue Date
1997-06-03
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Citation
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, v.7, no.11, pp.1475 - 1480
Abstract
Novel 1,3-dioxolanyl-, 1,3-oxathiolanyl- and 1,3-dithiolanylnucleosides with 2-hydroxymethyl substituents (1a-4b) were each synthesized with good yields through the condensation of dinucleophiles (oxygen and/or sulfur) with 1,3-dibenzoxy-2-propanone methyl ketal as a key step. (C) 1997 Elsevier Science Ltd.
Keywords
HUMAN-IMMUNODEFICIENCY-VIRUS; POTENT ANTI-HIV; NUCLEOSIDE ANALOGS; INFECTIVITY; OXETANOCIN; HBV; HUMAN-IMMUNODEFICIENCY-VIRUS; POTENT ANTI-HIV; NUCLEOSIDE ANALOGS; INFECTIVITY; OXETANOCIN; HBV
ISSN
0960-894X
URI
https://pubs.kist.re.kr/handle/201004/143738
DOI
10.1016/S0960-894X(97)00250-3
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KIST Article > Others
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