215862-10-5Relevant academic research and scientific papers
Chemoselective activation of nucleoside 3′-O-methylphosphonothioates with 1,3,5-triazinyl morpholinium salts
Wozniak, Lucyna A.,Gora, Marcin,Stec, Wojciech J.
, p. 8584 - 8587 (2007)
(Chemical Equation Presented) Chemoselective and stereospecific O-activation of 2′-deoxy-nucleoside 3′-O-methylphosphonothioates 5 with N-methyl-N-4,6-dimethoxy-1,3,5-triazin-2-yl morpholinium salts results in formation with retention of configuration of 5′-O-DMT-2′- deoxynucleoside 3′-O-(4,6 dimethoxy-1,3,5-triazin-2-yl methylphosphonothioates (7). Active esters 7 are convenient intermediates for hydrolytic interconversion of Rp-5 into Sp-5 and can be used as monomers for stereoselective synthesis of dinucleoside (3′,5′)-methyl phosphonothioates.
