Effects of preorganization and hydrogen bonding on intramolecular chemical ligation of (N)-and (O)-acyl isopeptides

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The ease of intramolecular N-to N-and O-to N-acyl transfers in (N)-acyl isopeptides and (O)-acyl isopeptides was found to be governed by preorganization rationalized in terms of geometrical and energetic characteristics of the linear isopeptide backbone, which depends on the chain length. Intramolecular hydrogen bonding was found another important factor of reactivity able to stabilize the chemical ligation transition state.

Original languageEnglish (US)
Pages (from-to)75-77
Number of pages3
JournalMendeleev Communications
Issue number2
StatePublished - 2014


ASJC Scopus subject areas

  • Chemistry(all)

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