Issue 1, 1995

Total synthesis of 2′-deoxy-2′-arafluorotoyocamycin and related nucleosides

Abstract

Total synthesis of 2′-deoxy-2′-arafluoro analogues of toyocamycin 11, sangivamycin 12 and thiosangivamycin 13, starting from 5-bromo-2-ethoxymethyleneaminopyrrole-3,4-dicarbonitrile 4 has been accomplished for the first time.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1995, 115-116

Total synthesis of 2′-deoxy-2′-arafluorotoyocamycin and related nucleosides

B. K. Bhattacharya and G. R. Revankar, J. Chem. Soc., Chem. Commun., 1995, 115 DOI: 10.1039/C39950000115

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