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Nucleic Acids Res. 1996 Aug 1;24(15):3115-7. doi: 10.1093/nar/24.15.3115.
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[Directed introduction of amino groups by internucleotide phosphate group during solid-phase synthesis of oligodeoxyribonucleotides. Preparation of biotinylated oligonucleotide probes].[寡脱氧核糖核苷酸固相合成过程中通过核苷酸间磷酸基团定向引入氨基。生物素化寡核苷酸探针的制备]
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7
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本文引用的文献

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Oligodeoxyribonucleotide phosphotriesters.寡脱氧核糖核苷酸磷酸三酯。
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A survey of nucleic acid services in core laboratories.核心实验室核酸检测服务调查
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3
Labile exocyclic amine protection of nucleosides in DNA, RNA and oligonucleotide analog synthesis facilitating N-deacylation, minimizing depurination and chain degradation.在DNA、RNA和寡核苷酸类似物合成中对核苷进行不稳定的环外胺保护,有助于N-脱酰化,使脱嘌呤和链降解最小化。
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4
The final deprotection step in oligonucleotide synthesis is reduced to a mild and rapid ammonia treatment by using labile base-protecting groups.通过使用不稳定的碱基保护基团,寡核苷酸合成中的最终脱保护步骤简化为温和且快速的氨处理。
Nucleic Acids Res. 1987 Jan 26;15(2):397-416. doi: 10.1093/nar/15.2.397.
5
The isopropoxyacetic group for convenient base protection during solid-support synthesis of oligodeoxyribonucleotides and their triester analogs.异丙氧基乙酰基用于在寡脱氧核糖核苷酸及其三酯类似物的固相合成过程中方便地进行碱基保护。
Nucleic Acids Res. 1989 Jun 26;17(12):4863-71. doi: 10.1093/nar/17.12.4863.

从可控孔径玻璃载体上切割寡脱氧核糖核苷酸及其通过气态胺进行的快速脱保护。

Cleavage of oligodeoxyribonucleotides from controlled-pore glass supports and their rapid deprotection by gaseous amines.

作者信息

Boal J H, Wilk A, Harindranath N, Max E E, Kempe T, Beaucage S L

机构信息

Division of Hematologic Product, Center for Biologics Evaluation and Research, Food and Drug Administration, Bethesda, MD 20892, USA.

出版信息

Nucleic Acids Res. 1996 Aug 1;24(15):3115-7. doi: 10.1093/nar/24.15.3115.

DOI:10.1093/nar/24.15.3115
PMID:8760903
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC146024/
Abstract

A novel method for the deprotection of oligodeoxyribonucleotides has been developed. Gaseous amines such as ammonia or methylamine were employed under pressure to achieve mild and rapid deprotection conditions. For example, oligodeoxyribonucleotides having a (tert-butyl)phenoxyacetyl group for the protection of the exocyclic amino function of cytosine, adenine and guanine were released from controlled-pore glass supports and fully deprotected by ammonia or methylamine under gas phase conditions, at room temperature, within 35 or 2 min respectively.

摘要

已开发出一种用于寡脱氧核糖核苷酸脱保护的新方法。在压力下使用气态胺,如氨或甲胺,以实现温和且快速的脱保护条件。例如,具有(叔丁基)苯氧基乙酰基用于保护胞嘧啶、腺嘌呤和鸟嘌呤的环外氨基功能的寡脱氧核糖核苷酸,从可控孔径玻璃载体上释放出来,并在室温下分别于35分钟或2分钟内在气相条件下用氨或甲胺完全脱保护。