MeOTf-Induced Carboannulation of Isothiocyanates and Aryl Alkynes with C═S Bond Cleavage: Access to Indenones

Org Lett. 2015 Sep 4;17(17):4388-91. doi: 10.1021/acs.orglett.5b02201. Epub 2015 Aug 19.

Abstract

MeOTf-induced carboannulation of alkyl isothiocyanates and aryl alkynes for the synthesis of indenones in good yields under metal-free conditions with C═S bond cleavage is described. The thioalkoxy group at the 3-position of the indenone can also be converted into other functional groups, such as phenyl, methylsulfonyl, amino, and ethoxy groups.

Publication types

  • Research Support, Non-U.S. Gov't