Re-Evaluating Chalcogen Bonding Trends: Catalytic Performance of Chaclonium(IV) Salts in the Povarov [4+2] Cycloaddition Reaction

This study investigates the catalytic activity of three chalconium salts Ar3Ch+OTf– (Ch = SIV, SeIV, TeIV) in the Povarov [4+2] cycloaddition reaction of N-phenyl-1-(p-tolyl)methanimine and 2,3-dihydrofuran. Kinetic experiments revealed that, in contrast to the established trends, a sulfur-based catalyst (Cat1OTf) displayed the highest activity, while selenium- and tellurium-based catalysts showed negligible activity. This unexpected outcome suggests that the imine activation may proceed via an alternative pathway, challenging traditional assumptions about the catalytic power of chalcogen bonding.

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Publication Details

Journal
Russian Journal of General Chemistry
Published
2024-11-01
DOI
https://doi.org/10.1134/s1070363224110124
Primary Topic
Organic Chemistry Cycloaddition Reactions
Type
article
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article

Re-Evaluating Chalcogen Bonding Trends: Catalytic Performance of Chaclonium(IV) Salts in the Povarov [4+2] Cycloaddition Reaction

Yana V. Safinskaya, Mikhail V. Il’in
Russian Journal of General Chemistry
Organic Chemistry Cycloaddition Reactions
article

Re-Evaluating Chalcogen Bonding Trends: Catalytic Performance of Chaclonium(IV) Salts in the Povarov [4+2] Cycloaddition Reaction

Yana V. Safinskaya, Mikhail V. Il’in
article en

Abstract

This study investigates the catalytic activity of three chalconium salts Ar3Ch+OTf– (Ch = SIV, SeIV, TeIV) in the Povarov [4+2] cycloaddition reaction of N-phenyl-1-(p-tolyl)methanimine and 2,3-dihydrofuran. Kinetic experiments revealed that, in contrast to the established trends, a sulfur-based catalyst (Cat1OTf) displayed the highest activity, while selenium- and tellurium-based catalysts showed negligible activity. This unexpected outcome suggests that the imine activation may proceed via an alternative pathway, challenging traditional assumptions about the catalytic power of chalcogen bonding.

Russian Journal of General ChemistryVol. 94(11)
St Petersburg University (RU)
Openalex Percentile: Top 83%
Organic Chemistry Cycloaddition Reactions
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