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Merck

A safe and practical procedure for global deprotection of oligoribonucleotides.

The Journal of organic chemistry (2010-07-31)
Daniel Zewge, Francis Gosselin, Rick Sidler, Lisa DiMichele, Raymond J Cvetovich
ABSTRAKT

We report a practical global deprotection of RNA 2'-O-tert-butyldimethylsilyl (TBS) ethers using commercially available aqueous NH(4)F. The procedure is applicable to both 96-well plate format and large-scale production of RNA. This improved procedure provides a safe, mild, and cost-effective alternative to highly hazardous Et(3)N x 3 HF, a reagent commonly used in the routine synthesis of RNA.

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Sigma-Aldrich
Ammonium fluoride, ≥99.99% trace metals basis
Sigma-Aldrich
Ammonium fluoride, ACS reagent, ≥98.0%
Sigma-Aldrich
Ammonium hydrogen difluoride, 99.999% trace metals basis
Sigma-Aldrich
Ammonium hydrogen difluoride, reagent grade, 95%