One-pot tandem epoxidation and rearrangement of styrenes to phenylacetaldehydes over a bifunctional metal-organic layer catalyst

Pengkun Su; Yuhang Song; Huihui Hu; Cheng Wang

doi:10.1039/d5cc07141k

January 1, 2026Chemical Communications

One-pot tandem epoxidation and rearrangement of styrenes to phenylacetaldehydes over a bifunctional metal-organic layer catalyst

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Key Points

The aim is to create an efficient method for converting styrene to phenylacetaldehyde using a metal-organic layer catalyst.
Developed a tandem catalytic strategy using a metal-organic layer (MOL) catalyst.
Integrated dual functional active sites within the catalyst for enhanced reactivity.
Conducted reaction trials to assess conversion efficiency.
Achieved high conversion rates of styrene to phenylacetaldehyde.
Demonstrated the potential of the MOL catalyst in facilitating this tandem reaction.

Implication

New catalyst efficiently converts styrene into phenylacetaldehyde, suggesting a promising synthetic pathway.

Abstract

This study develops an efficient tandem catalytic strategy for the direct conversion of styrene into phenylacetaldehyde. The process employs a well-designed metal-organic layer (MOL) catalyst integrated with dual functional active...

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Cite This Study

Su et al. (2026) studied this question.

synapsesocial.com/papers/69c37af0b34aaaeb1a67cf21 https://doi.org/10.1039/d5cc07141k

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One-pot tandem epoxidation and rearrangement of styrenes to phenylacetaldehydes over a bifunctional metal-organic layer catalyst

Key Points

Implication

Abstract

Discussion

Cite This Study

One-pot tandem epoxidation and rearrangement of styrenes to phenylacetaldehydes over a bifunctional metal-organic layer catalyst

Key Points

Implication

Abstract

Discussion

Cite This Study

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