A three-step, one-pot strategy to unsymmetrical 1,1-diarylalkenes

Develop a one-pot, three-step procedure for effective access to diverse unsymmetrical 1,1-diarylalkenes from readily accessible reagents, catalysts and substrates. A three-step, one-pot procedure for the synthesis of unsymmetrical 1,1-diarylalkenes via a dibromination-elimination-Suzuki Miyaura coupling sequence has been designed and a range of reaction conditions have been screened. Although high selectivities can be achieved in some cases, the overall reaction typically proceeds in low to moderate isolated yields albeit up to 70% was observed. The reaction is compatible with a range of substituent patterns on the arylboronic acid and different styrenes.

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Publication Details

Journal
BMC Research Notes
Published
2025-11-10
DOI
https://doi.org/10.1186/s13104-025-07553-0
Primary Topic
Catalytic Cross-Coupling Reactions
Type
article
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article

A three-step, one-pot strategy to unsymmetrical 1,1-diarylalkenes

Jørn H. Hansen, Stian Rølvaag Martinsen, Vijayaragavan Elumalai, Hanna Bähr et al.
BMC Research Notes
Catalytic Cross-Coupling Reactions
article

A three-step, one-pot strategy to unsymmetrical 1,1-diarylalkenes

Jørn H. Hansen, Stian Rølvaag Martinsen, Vijayaragavan Elumalai, Hanna Bähr, Karoline Nordli, Cole Funk
article en

Abstract

Develop a one-pot, three-step procedure for effective access to diverse unsymmetrical 1,1-diarylalkenes from readily accessible reagents, catalysts and substrates. A three-step, one-pot procedure for the synthesis of unsymmetrical 1,1-diarylalkenes via a dibromination-elimination-Suzuki Miyaura coupling sequence has been designed and a range of reaction conditions have been screened. Although high selectivities can be achieved in some cases, the overall reaction typically proceeds in low to moderate isolated yields albeit up to 70% was observed. The reaction is compatible with a range of substituent patterns on the arylboronic acid and different styrenes.

BMC Research NotesVol. 18(1)
Chemical Synthesis Lab (SG), UiT The Arctic University of Norway (NO)
Openalex Percentile: Top 75%
Catalytic Cross-Coupling Reactions
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A three-step, one-pot strategy to unsymmetrical 1,1-diarylalkenes — Jørn H. Hansen, Stian Rølvaag Martinsen, et al. · BMC Research Notes (2025) | TGRS Research Map | TGRS