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A straightforward synthesis of 5'-peptide oligonucleotide conjugates using N(alpha)-Fmoc-protected amino acids.

作者信息

Ocampo Sandra M, Albericio Fernando, Fernández Irene, Vilaseca Marta, Eritja Ramon

机构信息

Institut de Biologia Molecular de Barcelona, CSIC, Jordi Girona 18-26, E-08034 Barcelona, Spain.

出版信息

Org Lett. 2005 Sep 29;7(20):4349-52. doi: 10.1021/ol0514698.

DOI:10.1021/ol0514698
PMID:16178530
Abstract

[reaction: see text] 5'-Peptide oligonucleotide conjugates were prepared stepwise on a single support using N(alpha)-Fmoc-protected amino acids and unprotected phosphate groups. The method uses commercially available reagents and is successful with most natural amino acids. The simplicity of the method may encourage researchers to prepare new oligonucleotide-peptide conjugates with novel properties.

摘要

相似文献

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A straightforward synthesis of 5'-peptide oligonucleotide conjugates using N(alpha)-Fmoc-protected amino acids.
Org Lett. 2005 Sep 29;7(20):4349-52. doi: 10.1021/ol0514698.
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An activated triple bond linker enables 'click' attachment of peptides to oligonucleotides on solid support.
一个活化的三键连接子使得在固体载体上的寡核苷酸能够通过点击反应连接到肽上。
Nucleic Acids Res. 2011 Nov 1;39(20):9047-59. doi: 10.1093/nar/gkr603. Epub 2011 Jul 27.
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Diels-Alder cycloadditions in water for the straightforward preparation of peptide-oligonucleotide conjugates.在水中进行狄尔斯-阿尔德环加成反应以直接制备肽-寡核苷酸缀合物。
Nucleic Acids Res. 2006 Feb 14;34(3):e24. doi: 10.1093/nar/gnj020.