Removal of t-butyldimethylsilyl protection in RNA-synthesis. Triethylamine trihydrofluoride (TEA, 3HF) is a more reliable alternative to tetrabutylammonium fluoride (TBAF)

. 1994 Jun 25;22(12):2430–2431. doi: 10.1093/nar/22.12.2430

Removal of t-butyldimethylsilyl protection in RNA-synthesis. Triethylamine trihydrofluoride (TEA, 3HF) is a more reliable alternative to tetrabutylammonium fluoride (TBAF).

PMCID: PMC523709 PMID: 7518583

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Gasparutto D., Livache T., Bazin H., Duplaa A. M., Guy A., Khorlin A., Molko D., Roget A., Téoule R. Chemical synthesis of a biologically active natural tRNA with its minor bases. Nucleic Acids Res. 1992 Oct 11;20(19):5159–5166. doi: 10.1093/nar/20.19.5159. [DOI] [PMC free article] [PubMed] [Google Scholar]
Hogrefe R. I., McCaffrey A. P., Borozdina L. U., McCampbell E. S., Vaghefi M. M. Effect of excess water on the desilylation of oligoribonucleotides using tetrabutylammonium fluoride. Nucleic Acids Res. 1993 Oct 11;21(20):4739–4741. doi: 10.1093/nar/21.20.4739. [DOI] [PMC free article] [PubMed] [Google Scholar]
Rozners E., Westman E., Strömberg R. Evaluation of 2'-hydroxyl protection in RNA-synthesis using the H-phosphonate approach. Nucleic Acids Res. 1994 Jan 11;22(1):94–99. doi: 10.1093/nar/22.1.94. [DOI] [PMC free article] [PubMed] [Google Scholar]
Stawinski J., Strömberg R., Thelin M., Westman E. Studies on the t-butyldimethylsilyl group as 2'-O-protection in oligoribonucleotide synthesis via the H-phosphonate approach. Nucleic Acids Res. 1988 Oct 11;16(19):9285–9298. doi: 10.1093/nar/16.19.9285. [DOI] [PMC free article] [PubMed] [Google Scholar]