Mild arming and derivatization of natural products via an In(OTf)3-catalyzed arene iodination

Org Lett. 2010 May 7;12(9):2104-7. doi: 10.1021/ol100587j.

Abstract

Iodination of arene-containing natural products employing N-iodosuccinimide catalyzed by In(OTf)(3) at ambient temperature is reported as a versatile and mild method for natural product derivatization amenable to small scale. This process facilitates natural product derivatization of arene moieties for SAR studies, homo- and heterodimerization of natural products, and also conjugation with reporters such as biotin via subsequent metal-mediated coupling reactions.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biological Products / chemistry*
  • Catalysis
  • Indium / chemistry*
  • Structure-Activity Relationship
  • Succinimides / chemistry
  • Temperature

Substances

  • Biological Products
  • Succinimides
  • Indium
  • N-iodosuccinimide