Enantioselective Synthesis of [6]Carbohelicenes

J Am Chem Soc. 2017 Feb 1;139(4):1428-1431. doi: 10.1021/jacs.6b12443. Epub 2017 Jan 23.

Abstract

The use of α-cationic phosphonites derived from TADDOL as ancillary ligands has allowed a highly regio- and enantioselective synthesis of substituted [6]carbohelicenes by sequential Au-catalyzed intramolecular hydroarylation of diynes. Key for these results is the modular structure of these new ligands, and the enhanced reactivity that they impart to Au(I)-centers after coordination.

Publication types

  • Research Support, Non-U.S. Gov't