Nucleosides and Nucleotides · 1993 · 12 citations · 24 references
Natural SciencesChemistryNatural Product BiosynthesisNucleic Acid ChemistryOrganometallic ChemistryAmino Acid ChemistryOrganic SynthesisAmine FunctionalizationNucleoside Analog SynthesisThymidylate Synthesis
Abstract A series of 3′-N-substituted 3′-amino-3′-deoxythymidine derivatives with alkyl, alkenyl and alkylaryl substituents was synthesized by two methods. The first method involved the reaction of 1-(2,3-dideoxy-3-0-mesyl-5-0-trityl-β-D-threo-pentofuranosyl)thymine with an appropriate amine. In the second method, 3′-amino-5′-0-trityl-3′-deoxy-thymidine served as a synthetic precursor which was reacted with an appropiate aldehyde or ketone followed by sodium borohydride reduction. An improved synthesis of 3′-amino-3′-deoxythymidine from 3′ -azido-5′-0-trityl-3′-deoxythymidine using sodium borohydride was also described.
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Hiroaki Mitsuya, Kent J. Weinhold, P A Furman et al. · Proceedings of the National Academy of Sciences · 1985 · 1.9K citations · Full text
Ying‐Chih Cheng, Ginger E. Dutschman, Kenneth F. Bastow et al. · Journal of Biological Chemistry · 1987 · 227 citations · Full text