The Divergent Reactivity of Acid Chlorides Under Transition Metal Catalysis

The power and ability of catalysis to build multiple C-C bonds in a single step has had a transformative impact on organic synthesis. While the reactivity of organohalides with metal catalysts is widely appreciated, the related and more intricate reactivity of acid chlorides is less so, despite their use as common reagents in synthesis. Here, we review the transformations of acid chlorides in combination with unsaturated C-C bonds catalyzed by palladium, rhodium, or iridium and provide an outlook for future research opportunities.

Publication Details

Journal
Repository for Publications and Research Data (ETH Zurich)
Published
2024-12-02
DOI
https://doi.org/10.3929/ethz-b-000706681
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
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article

The Divergent Reactivity of Acid Chlorides Under Transition Metal Catalysis

Repository for Publications and Research Data (ETH Zurich)
Catalytic C–H Functionalization Methods
article

The Divergent Reactivity of Acid Chlorides Under Transition Metal Catalysis

article en

Abstract

The power and ability of catalysis to build multiple C-C bonds in a single step has had a transformative impact on organic synthesis. While the reactivity of organohalides with metal catalysts is widely appreciated, the related and more intricate reactivity of acid chlorides is less so, despite their use as common reagents in synthesis. Here, we review the transformations of acid chlorides in combination with unsaturated C-C bonds catalyzed by palladium, rhodium, or iridium and provide an outlook for future research opportunities.

Repository for Publications and Research Data (ETH Zurich)
Openalex Percentile: Top 78%
Catalytic C–H Functionalization Methods
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The Divergent Reactivity of Acid Chlorides Under Transition Metal Catalysis · Repository for Publications and Research Data (ETH Zurich) (2024) | TGRS Research Map | TGRS