Iron-Catalyzed Nitrene Transfer Reactions Enabled by Hydroxylamine Derivatives.

The synthesis of nitrogen-containing compounds and heterocycles is of central importance in organic chemistry, as many biologically active molecules contain at least one C-N bond. Among the various strategies available for C-N bond formation, transition-metal-catalyzed nitrene transfer has emerged as a versatile approach. Although numerous nitrene precursors and catalytic systems have been developed over the years, increasing attention has recently been devoted to more sustainable methodologies. In this context, we have developed a range of iron-catalyzed nitrene transfer reactions employing hydroxylamine-derived reagents as nitrene precursors, thereby providing attractive and sustainable alternatives to conventional systems based on noble-metal catalysts and iminoiodinane or azide reagents.

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Journal
Synlett
Published
2026-09-09
DOI
https://doi.org/10.1055/a-2956-2695
Primary Topic
Synthesis and Catalytic Reactions
Type
article
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article

Iron-Catalyzed Nitrene Transfer Reactions Enabled by Hydroxylamine Derivatives.

Guillaume Prestat, Farouk Berhal
Synlett
Synthesis and Catalytic Reactions
article

Iron-Catalyzed Nitrene Transfer Reactions Enabled by Hydroxylamine Derivatives.

Guillaume Prestat, Farouk Berhal
article en

Abstract

The synthesis of nitrogen-containing compounds and heterocycles is of central importance in organic chemistry, as many biologically active molecules contain at least one C-N bond. Among the various strategies available for C-N bond formation, transition-metal-catalyzed nitrene transfer has emerged as a versatile approach. Although numerous nitrene precursors and catalytic systems have been developed over the years, increasing attention has recently been devoted to more sustainable methodologies. In this context, we have developed a range of iron-catalyzed nitrene transfer reactions employing hydroxylamine-derived reagents as nitrene precursors, thereby providing attractive and sustainable alternatives to conventional systems based on noble-metal catalysts and iminoiodinane or azide reagents.

Synlett
Université Paris Cité (FR), Sorbonne Paris Cité (FR)
Responsible consumption and production
Openalex Percentile: Top 20%
Synthesis and Catalytic Reactions
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Iron-Catalyzed Nitrene Transfer Reactions Enabled by Hydroxylamine Derivatives. — Guillaume Prestat, Farouk Berhal · Synlett (2026) | TGRS Research Map | TGRS