219692-88-3Relevant academic research and scientific papers
Synthesis and deprotection of β-silylethyl protected O,O,O-and O,O,S-trialkylphosphorothioates
Krotz, Achim H.,Cole, Douglas L.,Ravikumar, Vasulinga T.
, p. 1999 - 2002 (2007/10/03)
Functionalized 2-(diphenylmethylsilyl)ethyl protected thymidyl-thymidine phosphorothioate dimers are easily accessible and stable under conditions used in oligophosphorothioate synthesis. Deprotection with ammonium hydroxide occurs through β-fragmentation. Methylamine and tetrabutyl-ammonium fluoride rapidly and selectively remove the DPSE protecting group of O,O,O-and O,O,S-trialkylphosphorothioates.
