Synthesis and Potent Anti-leukemic Activity of Novel 5 '-Norcarbocyclic C-nucleoside Phosphonic Acids

Authors
Kim, SeyeonKim, EunaeOh, Chang-HyunYoo, Kyung HoHong, Joon Hee
Issue Date
2014-12-20
Publisher
WILEY-V C H VERLAG GMBH
Citation
BULLETIN OF THE KOREAN CHEMICAL SOCIETY, v.35, no.12, pp.3502 - 3508
Abstract
The first synthetic route to 5'-norcarbocyclic C-nucleoside [7-oxa-7,9-dideazadenosine (furo[3,2-d]pyrimidine) and 9-deazaadenosine (pyrrolo[3,2-d]pyrimidine)] phosphonic acids from commercially available 1,3dihydroxy cyclopentane was described. The key C-C bond formation from sugar to base precursor was performed using Knoevenagel-type condensation from a ketone derivative. Synthesized C-nucleoside phosphonic acids were tested for anti-HIV activity as well as anti-leukemic activity. Compound 26 showed significant anti-leukemic activity.
Keywords
ENANTIOSELECTIVE SYNTHESIS; ANTIVIRAL ACTIVITY; NUCLEOTIDE ANALOGS; FACILE SYNTHESIS; ADENOSINE; ENANTIOSELECTIVE SYNTHESIS; ANTIVIRAL ACTIVITY; NUCLEOTIDE ANALOGS; FACILE SYNTHESIS; ADENOSINE; Antiviral agent; Anti-leukemic agent; C-nucleoside; Knoevenagel reaction
ISSN
0253-2964
URI
https://pubs.kist.re.kr/handle/201004/125980
DOI
10.5012/bkcs.2014.35.12.3502
Appears in Collections:
KIST Article > 2014
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE