B. Sproat et al., AN EFFICIENT METHOD FOR THE ISOLATION AND PURIFICATION OF OLIGORIBONUCLEOTIDES, Nucleosides & nucleotides, 14(1-2), 1995, pp. 255-273
Problems associated with the use of tetrabutylammonium fluoride like i
ncomplete desilylation and removal of the tetrabutylammonium salts dur
ing large scale syntheses of oligoribonucleotides (RNA) have been elim
inated by the use of triethylamine trihydrofluoride and precipitation
of the RNA with 1-butanol. An efficient anion-exchange HPLC method has
been developed for the purification of chemically synthesized RNA and
the resulting product precipitated directly by the addition of 1-prop
anol. A new activator, 5-ethylthio-1H-tetrazole significantly enhances
the synthesis quality and yield of oligoribonucleotides. RNA synthesi
zed using these improvements has been