Ex post glycoconjugation of phthalocyanines

J Org Chem. 2010 Jun 4;75(11):3859-62. doi: 10.1021/jo100362n.

Abstract

For the first time, fully fledged phthalocyanines (Pcs) were ex post glycoconjugated, that is, via 1,3-dipolar cycloaddition reaction. This divergent approach gains rapid access to a broad range of highly diverse Pcs bearing chemically sensitive substituents. This will be a breakthrough in generating structure-activity relationships (SAR) for the development of novel bioactive molecules.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Glycosylation
  • Indoles / chemistry*
  • Isoindoles
  • Radiation-Sensitizing Agents
  • Structure-Activity Relationship

Substances

  • Indoles
  • Isoindoles
  • Radiation-Sensitizing Agents
  • phthalocyanine