Substituent--directed aralkylation and alkylation reactions of the tricyclic analogues of acyclovir and guanosine

Nucleosides Nucleotides Nucleic Acids. 2000 Oct-Dec;19(10-12):1911-29. doi: 10.1080/15257770008045468.

Abstract

Aryl or tert-butyl substituent in the 6 position of 3,9-dihydro-3-[(2-hydroxyethoxy)methyl]-9-oxo-6-R-5H-imidazo[1,2-a]purine (6-R-TACV) 1 partly directs aralkylation reactions into unusual positions: N-4 to give 3 and C-7 to give N-5,7-disubstituted or N-4,7-disubstituted derivatives. In the case of alkylation the effect is limited to aryl substituent and position N-4. Replacement of acyclic moiety of 1 with a ribosyl one like in 7 prevents N-4 substitution. Cleavage of the third ring of 3b to give 3-benzylacyclovir 10 is an example of a new short route to 3-aralkyl-9-substituted guanines.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acyclovir / analogs & derivatives
  • Acyclovir / chemistry*
  • Alkylation
  • Guanosine / analogs & derivatives
  • Guanosine / chemistry*
  • Spectrum Analysis

Substances

  • Guanosine
  • Acyclovir