Skip to content
2000
Volume 18, Issue 1
  • ISSN: 1385-2728
  • E-ISSN: 1875-5348

Abstract

Bioorthogonal ligations have found widespread use in biomedical research for site selective labeling of biomolecules in living systems. Discovering new reactions to expand the toolbox of bioorthogonal chemistry remains an important, yet challenging task as most reactions do not meet the stringent requirements of bioorthogonal reaction. As highly useful synthetic intermediates, ortho-quinone methides (oQMs) have been broadly utilized in the total synthesis of natural products but have rarely been applied to biological studies. The required harsh reaction condition to generate oQMs would be detrimental to the cell or living organism. In this highlight, we would like to describe our recent development of a new bioorthogonal ligation enabled by the “click” cycloaddition of ortho-quinolinone quinone methide (oQQM) and vinyl thioether (VT).

Loading

Article metrics loading...

/content/journals/coc/10.2174/138527281801140121123419
2014-01-01
2025-05-24
Loading full text...

Full text loading...

/content/journals/coc/10.2174/138527281801140121123419
Loading
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test