Issue 8, 2019

Enynone-enabled migratory insertion and Schmittel cyclization cascade for the synthesis of furan-fused fluorenes

Abstract

A new method for the synthesis of furan-/benzo-fused fluorenes through copper(I)-catalyzed coupling of conjugated enynones or α-diazocarbonyl compounds with dialkynylbenzenes has been developed. This process includes 5-exo-dig cyclization, carbene migratory insertion, Schmittel cyclization and 1,5-H transfer. The obvious advantages of wide substrate scopes, mild reaction conditions, and high atom efficiency make this system highly appealing for the construction of six-substituted benzofuran-embedded fluorenes in a one-pot manner.

Graphical abstract: Enynone-enabled migratory insertion and Schmittel cyclization cascade for the synthesis of furan-fused fluorenes

Supplementary files

Article information

Article type
Research Article
Submitted
10 Jan 2019
Accepted
19 Feb 2019
First published
21 Feb 2019

Org. Chem. Front., 2019,6, 1118-1122

Enynone-enabled migratory insertion and Schmittel cyclization cascade for the synthesis of furan-fused fluorenes

H. Zhang, T. Cao, H. Luo, L. Chen and S. Zhu, Org. Chem. Front., 2019, 6, 1118 DOI: 10.1039/C9QO00045C

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