Synthesis of oligoribonucleotides using 4-methoxybenzyl group as a new protecting group of the 2′-hydroxyl group of adenosine
H Takaku, K Kamaike
Index: Takaku, Hiroshi; Kamaike, Kazuo Chemistry Letters, 1982 , p. 189 - 192
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Citation Number: 43
Abstract
4-Methoxybenzyl group was introduced directly to the 2′-hydroxyl group from the reaction of adenosine with 4-methoxybenzyl bromide in the presence of sodium hydride. The 2′-O- (4-methoxybenzyl) adenosine can be successfully used in the synthesis of oligoribonucleotides via phosphotriester approach. The 4-methoxybenzyl group was removed rapidly from the oligoribonucleotides by triphenylmethyl fluoroborate and the ...
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