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Article in English | MEDLINE | ID: mdl-11991147

ABSTRACT

Two enantiomerically pure hydroxymethyl substituted cyclopentene nucleoside analogues (42 and 53) related to carbovir and neplanocin A, respectively, were prepared from the chiral pool of iridoid glucosides. In addition two saturated hydroxymethylated analogues (44 and 45) were obtained from a protected intermediate.


Subject(s)
Adenosine/analogs & derivatives , Adenosine/chemistry , Dideoxynucleosides/chemistry , Nucleosides/chemical synthesis
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