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Silyl protecting groups for oligonucleotide synthesis removed by a ZnBr2 treatment.

作者信息

Ferreira Fernando, Morvan François

机构信息

Laboratoire de Chimie Organique Biomoléculaire de Synthèse, UMR 5625 CNRS-UM II, Université de Montpellier U1, Place E. Bataillon, 34095 Montpellier Cedex 5, France.

出版信息

Nucleosides Nucleotides Nucleic Acids. 2005;24(5-7):1009-13. doi: 10.1081/ncn-200060342.

Abstract

An oligonucleotide protected with N-(trimethylsilyloxycarbonyl) (Teoc) and P-(trimethylsilylethanol) (Tse) groups was synthesized and deprotected by a single ZnBr2 treatment. Finally it was released from the solid support by cleavage of a disulfide linkage with TCEP. The olgonucleotide was obtained without any basic treatment.

摘要

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