-transparent.png){kind=logo}
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.
Related Publications
D Viña, and
L Santana, and
E Uriarte
September 2002,
European journal of medicinal chemistry,
D Viña, and
L Santana, and
E Uriarte
September 1986,
Journal of medicinal chemistry,
D Viña, and
L Santana, and
E Uriarte
September 1981,
Journal of medicinal chemistry,
D Viña, and
L Santana, and
E Uriarte
January 2003,
Nucleosides, nucleotides & nucleic acids,
D Viña, and
L Santana, and
E Uriarte
October 1984,
Journal of medicinal chemistry,
D Viña, and
L Santana, and
E Uriarte
September 2001,
Chemical & pharmaceutical bulletin,
D Viña, and
L Santana, and
E Uriarte
January 1986,
Medicinal research reviews,
D Viña, and
L Santana, and
E Uriarte
February 1983,
Journal of medicinal chemistry,
D Viña, and
L Santana, and
E Uriarte
July 1995,
Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme,
D Viña, and
L Santana, and
E Uriarte
May 1998,
Bioorganic & medicinal chemistry letters,
