195307-35-8Relevant articles and documents
Triarylmethyl substituted 4,5-dicyanoimidazoles as activators for Rp- diastereoselective synthesis of TpN dinucleoside methylphosphonates
Schell, Peter,Laux, Wolfgang H. G.,Engels, Joachim W.
, p. 1169 - 1174 (1999)
2-Triarylmethyl-4,5-dicyanoimidazoles 1-3 were synthesized and tested as activators in the methylphosphonamidite approach. TpN dinucleoside methylphosphonates generated showed diastereoselectivity of up to 8/1 (Rp/Sp). The influence of the different triarylmethyl substituents on diastereoselectivity is shown.
Methylphosphonate modified hairpin loops
Schweitzer, Markus,Engels, Joachim W.
, p. 317 - 326 (2007/10/03)
We synthesized and analyzed DNA hairpin molecules with methylphosphonate linkages of defined stereochemistry in the loop region. Dinucleotide building blocks ApA and TpT (p indicating methylphosphonate linkage with either Rp or Sp configuration) were synt