113808-27-8Relevant articles and documents
USE OF 5-DEOXY-ribo-HEXOFURANOSE DERIVATIVES FOR THE PREPARATION OF 5'-NUCLEOTIDE PHOSPHONATES AND HOMORIBONUCLEOSIDES
Mikhailov, Sergei N.,Padyukova, Nelly Sh.,Karpeiskii, Marat Ya.,Kolobushkina, Lidiya I.,Beigelman, Leon N.
, p. 1055 - 1066 (2007/10/02)
A convenient and general method is proposed for the synthesis of 5'-nucleotide phosphonate analogs starting from 5-deoxy-1,2-O-isopropylidene-α-D-xylo-hexofuranose which can easily be produced in preparative quantities from D-glucose.Phosphonate IIIa was synthesized by means of the Arbuzov reaction between 3-O-benzoyl-6-bromo-5,6-dideoxy-1,2-O-isopropylidene-α-D-ribo-hexofuranose and triethyl phosphite.The consecutive acetolysis, condensation with uracil and N6-benzoyladenine bis-trimethylsilyl derivatives and deblocking possessed phosphonate analogs of 5'-nucleotides in good yields.The intermediate 5-deoxy-1,2-O-isopropylidene-α-D-ribo-hexofuranose derivatives were used for the preparation of homonucleosides.
A NEW SCHEME FOR THE SYNTHESIS OF 5'-NUCLEOTIDE PHOSPHONATE ANALOGS
Padyukova, Nelly Sh.,Karpeisky, Marat Ya.,Kolobushkina, Lidiya I.,Mikhailov, Sergey N.
, p. 3623 - 3626 (2007/10/02)
A convenient and general method is proposed for the synthesis of 5'-nucleotide phosphonate analogs starting from 5-deoxy-1,2-O-isopropylidene-α-D-xylo-hexofuranose (1).