Synthesis of the optically active carbocyclic analogs of the four 2'- deoxyribonucleoslde monophosphates

Article abstract of DOI:10.1080/07328319708002566

The (+)-enantiomer of the carbocyclic analogs of the four 2'-deoxy- ribonucleoside monophosphate constituents of DNA, C-dAMP² (1: A), C-dGMP (1: G), C-dCMP (1: C), and C-TMP (1: T) have been synthesized via the Mitsunobu coupling reaction. Two

Full text of DOI:10.1080/07328319708002566

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Nucleosides and Nucleotides
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Synthesis of the Optically Active
Carbocyclic Analogs of the Four 2′-
Deoxyribonucleoside Monophosphates
Laurent Schmitt a & Carol A. Caperelli a
a Division of Pharmaceutical Sciences , College of Pharmacy
University of Cincinnati , P.O. Box 670004, Cincinnati, OH,
45267-0004
Published online: 23 Aug 2006.
To cite this article: Laurent Schmitt & Carol A. Caperelli (1997) Synthesis of the Optically Active
Carbocyclic Analogs of the Four 2′-Deoxyribonucleoside Monophosphates, Nucleosides and
Nucleotides, 16:12, 2165-2192, DOI: 10.1080/07328319708002566
To link to this article: http://dx.doi.org/10.1080/07328319708002566
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