Synthesis and testing of new modified nucleosides

Article abstract of DOI:10.1080/15257779908041490

New efficient routes for the high-yielding synthesis of several classes of modified nucleosides have been developed. We have prepared both the D- and L-enantiomers of the methylene-expanded oxetanocin isonucleosides 1a-c and the L-2',3'-dideoxy isonucleosides 2abc (both the oxa and thia analogues) as well as new routes for the preparation of L-ribose and 2-deoxy L-ribose 3ab and their modified nucleosides 4.

Full text of DOI:10.1080/15257779908041490

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Nucleosides and Nucleotides
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Synthesis and Testing of New Modified
Nucleosides
Michael E. Jung a , Christopher J. Nichols a , Oliver Kretschik a & Yue
Xu a
a Department of Chemistry and Biochemistry , University of
California , Los Angeles, California, 90095-1569
Published online: 04 Oct 2006.
To cite this article: Michael E. Jung , Christopher J. Nichols , Oliver Kretschik & Yue Xu (1999)
Synthesis and Testing of New Modified Nucleosides, Nucleosides and Nucleotides, 18:4-5, 541-546,
DOI: 10.1080/15257779908041490
To link to this article: http://dx.doi.org/10.1080/15257779908041490
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