4.5 Article

Ortho-Quinone Methide Finds Its Application in Bioorthogonal Ligation

Journal

CURRENT ORGANIC CHEMISTRY
Volume 18, Issue 1, Pages 86-92

Publisher

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/138527281801140121123419

Keywords

Bioorthogonal ligation; ortho-quinone methide; vinyl thioether; chemical genetics; hetero-Diels-Alder cycloaddition; protein labeling

Funding

  1. National High Technology Projects 973 [2012CB837400]
  2. Program for New Century Excellent Talents in University [NCET-10-0614]
  3. NSFC [21072150, 21222209]

Ask authors/readers for more resources

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).

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available