Amino acid bioconjugation via iClick reaction of an oxanorbornadiene-masked alkyne with a Mn(I)(bpy)(CO)3-coordinated azide

Chem Commun (Camb). 2014 Dec 25;50(99):15692-5. doi: 10.1039/c4cc07892f. Epub 2014 Nov 5.

Abstract

The catalyst-free room temperature iClick reaction of an unsymmetrically 2,3-disubstituted oxanorbornadiene (OND) as a "masked" alkyne equivalent with [Mn(N3)(bpy(CH3,CH3))(CO)3] leads to isolation of a phenylalanine ester bioconjugate, in which the model amino acid is linked to the metal moiety via a N-2-coordinated triazolate formed in a cycloaddition-retro-Diels-Alder (crDA) reaction sequence, in a novel approach to bioorthogonal coupling reactions based on metal-centered reactivity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkynes / chemistry*
  • Amino Acids / chemistry*
  • Azides / chemistry*
  • Camphanes / chemistry*
  • Catalysis
  • Click Chemistry
  • Coordination Complexes / chemistry*
  • Crystallography, X-Ray
  • Cycloaddition Reaction
  • Manganese / chemistry
  • Molecular Conformation
  • Phenylalanine / chemistry
  • Temperature
  • Thermodynamics

Substances

  • Alkynes
  • Amino Acids
  • Azides
  • Camphanes
  • Coordination Complexes
  • Manganese
  • Phenylalanine