Target-driven selection in a dynamic nitrone library

Simon M. Turega, Christiane Lorenz, Jan W. Sadownik, Douglas Philp

Research output: Contribution to journalArticlepeer-review

Abstract

Nitrones undergo dynamic exchange in chloroform at room temperature through two mechanisms-hydrolysis and recombination or hydroxylamine addition/elimination, this dynamic exchange is harnessed to select a nitrone-based bis(amidopyridine) receptor for diacids from a group of four nitrones through its binding to a glutaric acid-based target.

Original languageEnglish
Pages (from-to)4076-4078
Number of pages3
JournalChemical Communications
Issue number34
DOIs
Publication statusPublished - 14 Sept 2008

Keywords

  • COMBINATORIAL LIBRARIES
  • CHEMISTRY
  • AMPLIFICATION
  • RECEPTORS
  • DISCOVERY
  • SENSORS
  • SYSTEM

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