Nucleic acid related compounds .91. Biomimetic reactions are in harmony with loss of 2'-substituents as free radicals (not anions) during mechanism-based inactivation of ribonucleotide reductases. Differential interactions of azide, halogen, and alkylthio groups with tributylstannane and triphenylsilane Article

Robins, MJ, Wnuk, SF, HernandezThirring, AE et al. (1996). Nucleic acid related compounds .91. Biomimetic reactions are in harmony with loss of 2'-substituents as free radicals (not anions) during mechanism-based inactivation of ribonucleotide reductases. Differential interactions of azide, halogen, and alkylthio groups with tributylstannane and triphenylsilane . JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 118(46), 11341-11348. 10.1021/ja962117m

cited authors

  • Robins, MJ; Wnuk, SF; HernandezThirring, AE; Samano, MC

sustainable development goals

authors

publication date

  • November 20, 1996

published in

keywords

  • 2'-AZIDO-2'-DEOXYURIDINE 5'-DIPHOSPHATE
  • 3'-AZIDO-3'-DEOXYTHYMIDINE AZT
  • ANTI-HIV ACTIVITY
  • CHAIN REACTIONS
  • Chemistry
  • Chemistry, Multidisciplinary
  • DIPHOSPHATE REDUCTASE
  • ESCHERICHIA-COLI
  • NUCLEOSIDES
  • ORGANIC-SYNTHESIS
  • POTENTIAL INHIBITORS
  • Physical Sciences
  • STEREOSPECIFIC SYNTHESIS
  • Science & Technology

Digital Object Identifier (DOI)

publisher

  • AMER CHEMICAL SOC

start page

  • 11341

end page

  • 11348

volume

  • 118

issue

  • 46