Aryl Silicon Nucleophiles in Bismuth Catalysis

We present a catalytic protocol utilizing bismuth for the synthesis of aromatic fluorinated thiosulfones, showcasing a seminal example of aryl silicon nucleophiles in Bi catalysis. This catalytic process is enabled by a series of Bi-based organometallic transformations, including an unprecedented transmetalation of aryl silicates to Bi(III) complexes and the formal migratory insertion of sulfur dioxide (SO<sub>2</sub>) into the Bi-C bond. The protocol is compatible with a wide range of anionic and neutral Ar-Si compounds, including heterocycles. Stoichiometric investigations of individual organometallic steps provide strong evidence supporting a Bi-redox-neutral catalytic cycle.

Authors

Institutions

Publication Details

Journal
Angewandte Chemie International Edition
Published
2025-02-11
DOI
https://doi.org/10.1002/anie.202424698
Citations
11
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
10.30

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Aryl Silicon Nucleophiles in Bismuth Catalysis

Josep Cornellà, Teresa Faber, Sophia Engelhardt
11 citations
Angewandte Chemie International Edition
Sulfur-Based Synthesis Techniques
10.30
article

Aryl Silicon Nucleophiles in Bismuth Catalysis

Josep Cornellà, Teresa Faber, Sophia Engelhardt
article en
11 citations

Abstract

We present a catalytic protocol utilizing bismuth for the synthesis of aromatic fluorinated thiosulfones, showcasing a seminal example of aryl silicon nucleophiles in Bi catalysis. This catalytic process is enabled by a series of Bi-based organometallic transformations, including an unprecedented transmetalation of aryl silicates to Bi(III) complexes and the formal migratory insertion of sulfur dioxide (SO<sub>2</sub>) into the Bi-C bond. The protocol is compatible with a wide range of anionic and neutral Ar-Si compounds, including heterocycles. Stoichiometric investigations of individual organometallic steps provide strong evidence supporting a Bi-redox-neutral catalytic cycle.

Angewandte Chemie International EditionVol. 64(13)
Max-Planck-Institut für Kohlenforschung (DE)
European Commission, Deutsche Forschungsgemeinschaft, Max-Planck-Gesellschaft
Openalex Percentile: Top 2%
Sulfur-Based Synthesis Techniques
10.30
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.