Issue 19, 2021

Matsuda–Heck arylation of itaconates: a versatile approach to heterocycles from a renewable resource

Abstract

Itaconic acid esters and hemiesters undergo Pd-catalyzed coupling reactions with arene diazonium salts in high to excellent yields. The coupling products of ortho-nitro arene diazonium salts can be converted in one or two steps to benzazepine-2-ones.

Graphical abstract: Matsuda–Heck arylation of itaconates: a versatile approach to heterocycles from a renewable resource

Supplementary files

Article information

Article type
Paper
Submitted
01 Mar 2021
Accepted
15 Apr 2021
First published
20 Apr 2021

Org. Biomol. Chem., 2021,19, 4292-4302

Matsuda–Heck arylation of itaconates: a versatile approach to heterocycles from a renewable resource

A. Krause, E. Sperlich and B. Schmidt, Org. Biomol. Chem., 2021, 19, 4292 DOI: 10.1039/D1OB00392E

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