Studies in the Solid Phase Synthesis of Oligo- and Poly-Ribonucleotides

Abstract
The solid phase synthesis of the 3′-terminal 10-mer, 19-mer and 37-mer sequences of unmodified yeast tRNAAla is described. The 2′- and 5′-hydroxy functions are protected, respectively, by the 1- (2-fluorophenyl)-4-methoxypiperidin-4-yl [Fpmp (11)] and 9-phenylxan-then-9-yl [px] groups, and 2-cyanoethyl di-isopropylphosphoramidite building blocks are used.

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