FormylBODIPYs: Privileged Building Blocks for Multicomponent Reactions. The Case of the Passerini Reaction

J Org Chem. 2016 Apr 1;81(7):2888-98. doi: 10.1021/acs.joc.5b02893. Epub 2016 Mar 22.

Abstract

Eleven formyl-containing BODIPY dyes were prepared by means of either the Liebeskind-Srogl cross-coupling reaction or the Vilsmeier reaction. These dyes were used as components in the Passerini reaction to give highly substituted BODIPY dyes. A joined spectroscopic and theoretical characterization of the synthesized compounds was conducted to unravel the impact of the structural rigidity/flexibility on the photophysical signatures. These dyes were tested as fluorescent trackers for phagocytosis. Additionally, they proved to be useful to stain different blood cells with an intense and stable signal at a very low exposure time.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Boron Compounds
  • Cytophagocytosis / drug effects
  • Fluorescent Dyes / chemistry*
  • Molecular Structure
  • Spectrophotometry, Ultraviolet

Substances

  • 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene
  • Boron Compounds
  • Fluorescent Dyes