Issue 3, 2025

Iridium-catalyzed tandem olefination/aza-Michael reaction: rapid access to N–N functionalized hydrazides

Abstract

An Ir-catalyzed tandem olefination/aza-Michael reaction of protected benzoylhydrazine derivatives with olefins under mild conditions has been developed. This method can be successfully applied to the construction of various structurally N–N-functionalized hydrazide derivatives bearing the α,β-unsaturated side chain in good to excellent yields. In particular, the deaminoprotected products can be used as potential precursors for the construction of N–N axially chiral compounds.

Graphical abstract: Iridium-catalyzed tandem olefination/aza-Michael reaction: rapid access to N–N functionalized hydrazides

Supplementary files

Article information

Article type
Paper
Submitted
09 окт 2024
Accepted
02 ноя 2024
First published
04 ноя 2024

Org. Biomol. Chem., 2025,23, 673-678

Iridium-catalyzed tandem olefination/aza-Michael reaction: rapid access to N–N functionalized hydrazides

C. Zhang and L. Dong, Org. Biomol. Chem., 2025, 23, 673 DOI: 10.1039/D4OB01631A

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