NUCLEOSIDE H-PHOSPHONATES - 18 - SYNTHESIS OF UNPROTECTED NUCLEOSIDE 5'-H-PHOSPHONATES AND NUCLEOSIDE 5'-H-PHOSPHONOTHIOATES AND THEIR CONVERSION INTO THE 5'-PHOSPHOROTHIOATE AND 5'-PHOSPHORODITHIOATE MONOESTERS
J. Jankowska et al., NUCLEOSIDE H-PHOSPHONATES - 18 - SYNTHESIS OF UNPROTECTED NUCLEOSIDE 5'-H-PHOSPHONATES AND NUCLEOSIDE 5'-H-PHOSPHONOTHIOATES AND THEIR CONVERSION INTO THE 5'-PHOSPHOROTHIOATE AND 5'-PHOSPHORODITHIOATE MONOESTERS, Journal of organic chemistry, 63(23), 1998, pp. 8150-8156
A simple and efficient protocol for the preparation of unprotected nuc
leoside 5'-H-phosphonates and nucleoside 5'-H-phosphonothioates via a
one-step deprotection of suitable precursors with methylamine has been
developed. The synthetic utility of the unprotected nucleotide deriva
tives was demonstrated by converting them under mild conditions to the
corresponding nucleoside 5'-phosphorothioate and nucleoside 5'-phosph
orodithioate monoesters. Factors affecting oxidation of H-phosphonate,
H-phosphonothioate, and phosphite derivatives with elemental sulfur a
re also discussed.