1,2-disubstituted cyclohexane carbocyclic analogues of nucleosides

Nucleosides Nucleotides Nucleic Acids. 2001 Apr-Jul;20(4-7):1363-5. doi: 10.1081/NCN-100002556.

Abstract

Several compounds of a new series of cyclohexane-based 1,2-disubstituted carbonucleoside analogues, were synthesized. The adenine and uridine derivatives, were prepared by construction of the heterocyclic base on the primary amino group of 2-aminocyclohexylmethanol, and the thymine derivative by condensation of 2-hydroxycyclohexylmethanol with thymine using the Mitsunobu reaction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenine / analogs & derivatives
  • Cyclohexanes / chemical synthesis*
  • Nucleosides / chemical synthesis*
  • Thymine / analogs & derivatives
  • Uridine / analogs & derivatives

Substances

  • Cyclohexanes
  • Nucleosides
  • Adenine
  • Thymine
  • Uridine