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Mechanisms and prevention of trifluoroacetylation in solid-phase peptide synthesis

A novel mechanism for trifluoroacetylation in solid-phase peptide synthesis, independent of the coupling step, has been elucidated. It involves the presence of trifluoroacetoxymethyl groups on the resin support, which react with resin-bound amines by an intersite nucleophilic reaction. The trifluoro...

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Vydáno v:Proc Natl Acad Sci U S A
Hlavní autoři: Kent, Stephen B. H., Mitchell, Alexander R., Engelhard, Martin, Merrifield, R. B.
Médium: Artigo
Jazyk:Inglês
Vydáno: National Academy of Sciences 1979
Témata:
On-line přístup:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC383561/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/287055/
https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.76.5.2180
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