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- W2167029347 abstract "Carboxamide functions may be tritylated by an acid-catalyzed reaction with triphenylmethanol and acetic anhydride in glacial acetic acid. The ω-trityl group of asparagine and glutamine is cleavable by TFA, but stable to strong mineral acids in aqueous solution, as well as to nucleophiles and bases. In peptide syntheses, it is ideally suited for combination with side-chain protections of the t.butyl-type." @default.
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- W2167029347 date "1991-02-01" @default.
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- W2167029347 title "Protection of carboxamide functions by the trityl residue. Application to peptide synthesis" @default.
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- W2167029347 doi "https://doi.org/10.1016/s0040-4039(00)74872-6" @default.
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