Polushin N N, Pashkova I N, Efimov V A
Shemyakin Institute of Bioorganic Chemistry, USSR Academy of Sciences, Moscow.
Nucleic Acids Symp Ser. 1991(24):49-50.
Two new rapid procedures for the full deprotection of synthetic oligonucleotides has been developed. We have successfully used the mixture of ethanolamine and ethanol (1:1) or pure ethanolamine for deprotection of oligonucleotides, prepared by different methods. In the case of oligonucleotides prepared by commonly used beta-cyanoethyl phosphoramidite and H-phosphonates method deprotection takes half an hour at 70 degrees C. We have found also that mixture of hydrazine, ethanolamine and methanol (1:3:3, v/v/v) can serve as a very efficient reagent for deprotection of oligonucleotides, prepared by beta-cyanoethyl phosphoramidite method with isopropoxyacetyl protecting group for cytosine residues. In this case deprotection time is 12-17 min at room temperature.
已经开发出两种用于合成寡核苷酸完全脱保护的新快速方法。我们已成功使用乙醇胺和乙醇的混合物(1:1)或纯乙醇胺对通过不同方法制备的寡核苷酸进行脱保护。对于通过常用的β-氰基乙基亚磷酰胺和H-膦酸酯方法制备的寡核苷酸,在70℃下脱保护需要半小时。我们还发现,肼、乙醇胺和甲醇的混合物(1:3:3,v/v/v)可作为一种非常有效的试剂,用于对通过β-氰基乙基亚磷酰胺方法制备的、胞嘧啶残基带有异丙氧基乙酰保护基的寡核苷酸进行脱保护。在这种情况下,室温下脱保护时间为12 - 17分钟。