Chemistry Letters p. 721 - 724 (1993)
Update date:2022-08-11
Topics:
Ueki, Masaaki
Nishigaki, Naohiko
Aoki, Hiroko
Tsurusaki, Takeshi
Katoh, Tsuyoshi
9-Fluorenylmethyloxycarbonyl (Fmoc) group can be quickly removed with tetrabutylammonium fluoride hydrate (TBAF*xH2O) in the presence of a large excess of phenylmethanethiol or 1-octanethiol. Subsequent oxidation of the thiol with bis(1-methyl-1H-tetrazol-5-yl) disulfide simultaneously inactivated the TBAF and enabled one-pot peptide bond elongation by the Fmoc strategy.
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