Recent Advances in the Cycloaddition Reactions of 2-Benzylidene-1-benzofuran-3-ones, and Their Sulfur, Nitrogen and Methylene Analogues

Chem Asian J. 2020 Sep 15;15(18):2838-2853. doi: 10.1002/asia.202000550. Epub 2020 Aug 26.

Abstract

Benzothiophene, benzofuran, indole, and indene derivatives are privileged heterocyclic motifs. These are present in a wide range of bioactive natural products and pharmaceutical drugs and are the subject of materials science research. However, the construction of benzothiophene, benzofuran, indole, and indene frameworks have been long-standing challenges to organic chemists. In this review, we classify the derivatives of four structures synthesized from 2-benzylidene-1-benzofuran-3-one and their analogues in terms of their ring size (from three- to ten-membered) and type (fused or spiro), as well as summarizing the developments of this field. Finally, we discuss the ring opening and 1,4-addition reactions.

Keywords: 2-benzylidene-1-benzofuran-3-one; 2-benzylidene-1-benzothiophen-3-one; cycloaddition reaction; heterocycle compounds •.

Publication types

  • Review