A NEW STRATEGY FOR SYNTHESIS OF THE DINUCLEOTIDE pdCpA: A CONVENIENT METHOD FOR THE DEPROTECTION OF CYANOETHYL, TBDMS, AND BENZOYL GROUPS IN ONE STEP AT HIGH PRESSURE

摘要

A new convenient method for the preparative-scale synthesis of the dinucleotide pdCpA was developed. This method takes advantage of the complete deprotection of cyanoethyl, TBDMS, and benzoyl groups in one step under high-pressure conditions in the final stage of the synthetic sequence.