Journal of the Chemical Society. Chemical communications p. 274 - 275 (1987)
Update date:2022-08-17
Topics:
Fujii, Nobutaka
Otaka, Akira
Ikemura, Osamu
Akaji, Kenichi
Funakoshi, Susumu
et al.
Trimethylsilyl trifluoromethanesulphonate in trifluoroacetic acid has been found to cleave, in the presence of thioaisole, a number of protecting groups currently employed in peptide synthesis, without significant side reactions and with a much faster rate of reaction than trifluoromethanesulphonic acid in trifluoroacetic acid; this new deprotecting reagent has been used in solution and solid phase peptide syntheses of neuromedin U-25 (a 25-residue peptide) and a rabbit stomach peptide (an 8-residue peptide), respectively.
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