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Chemical Compound Review

TBAF     tetrabutylazanium fluoride

Synonyms: PubChem3907, TBAF solution, AGN-PC-00FCB4, ACMC-1AILI, AG-E-62407, ...
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High impact information on tetrabutylazanium

  • The title product 9 p5'A(2'p5'A)(3) (tetramer 2-5A) was obtained through phosphorylation of the terminal 5'-hydroxy of the protected tetramer and removal of remaining protecting groups using concentrated ammonium hydroxide-ethanol (3:1, v/v) at 55 degrees C and tetrabutylammonium fluoride (TBAF) in THF at room temperature, respectively [1].
  • Convenient indole synthesis from 2-iodoanilines and terminal alkynes by the sequential Sonogashira reaction and the cyclization reaction promoted by tetrabutylammonium fluoride (TBAF) [2].

References

  1. Endowing RNase H-inactive antisense with catalytic activity: 2-5A-morphants. Zhou, L., Civitello, E.R., Gupta, N., Silverman, R.H., Molinaro, R.J., Anderson, D.E., Torrence, P.F. Bioconjug. Chem. (2005) [Pubmed]
  2. Convenient indole synthesis from 2-iodoanilines and terminal alkynes by the sequential Sonogashira reaction and the cyclization reaction promoted by tetrabutylammonium fluoride (TBAF). Suzuki, N., Yasaki, S., Yasuhara, A., Sakamoto, T. Chem. Pharm. Bull. (2003) [Pubmed]
 
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