Issue 6, 2024

Direct synthesis of phenanthrenyl triflates from 1-biphenylyl-2-diazo-2-aryl ketones and triflic anhydride

Abstract

A strategy for direct synthesis of phenanthrenyl triflates from 1-biphenylyl-2-diazo-2-aryl ketones and triflic anhydride is described. The reaction of 1-biphenylyl-2-diazo-2-aryl ketones with triflic anhydride proceeded smoothly in the presence of 2,6-di-tert-butylpyridine under mild conditions to produce phenanthrenyl triflates in high to excellent yields. The phenanthrenyl triflate products were demonstrated to be utilized as coupling partners in various coupling reactions. The proposed mechanism involves an intramolecular Friedel–Crafts reaction of a vinyl cation intermediate formed in situ.

Graphical abstract: Direct synthesis of phenanthrenyl triflates from 1-biphenylyl-2-diazo-2-aryl ketones and triflic anhydride

Supplementary files

Article information

Article type
Communication
Submitted
08 Dec 2023
Accepted
04 Jan 2024
First published
05 Jan 2024

Org. Biomol. Chem., 2024,22, 1141-1145

Direct synthesis of phenanthrenyl triflates from 1-biphenylyl-2-diazo-2-aryl ketones and triflic anhydride

Y. Liu, S. Zhang, X. Feng, X. Yu, Y. Yamamoto and M. Bao, Org. Biomol. Chem., 2024, 22, 1141 DOI: 10.1039/D3OB02005C

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