What question did this study set out to answer?

To explore a new catalytic method for the insertion of unactivated alkynes into C–F bonds of acyl fluorides.

May 15, 2026Chemical ScienceOpen Access

AgBF ₄ -Catalyzed Insertion of Unactivated Alkynes into C–F Bonds of Acyl Fluorides

View Full Paper

Ask AI

Bookmark

To explore a new catalytic method for the insertion of unactivated alkynes into C–F bonds of acyl fluorides.
Employing AgBF4 as a catalyst for the reaction of unactivated alkynes with acyl fluorides.
Focused on achieving C-F bond cleavage and reformation.
Successfully synthesized monofluoroalkenes through the C-F insertion process.
Demonstrated a general route applicable to various unactivated alkynes.

Implication

Randomized trial reports the effective formation of monofluoroalkenes from acyl fluorides, suggesting a new synthetic method.

Abstract

We report an AgBF4-catalyzed intermolecular C-F insertion of unactivated alkynes into acyl fluorides, providing a general route to monofluoroalkenes. This transformation enables both C-F bond cleavage and reformation without activated...

Discussion

No takes yet. Share an insight, caveat, or question.

Cite This Study

Emmei et al. (2026) studied this question.

synapsesocial.com/papers/6a06b9e2e7dec685947ac88b https://doi.org/10.1039/d6sc02480g

View Full Paper

Ask AI

Bookmark

Implication

Randomized trial reports the effective formation of monofluoroalkenes from acyl fluorides, suggesting a new synthetic method.

AgBF ₄ -Catalyzed Insertion of Unactivated Alkynes into C–F Bonds of Acyl Fluorides

Key Points

Implication

Abstract

Discussion

Cite This Study

AgBF ₄ -Catalyzed Insertion of Unactivated Alkynes into C–F Bonds of Acyl Fluorides

Key Points

Implication

Abstract

Discussion

Cite This Study

Keep reading

Keep reading