Supramolecular catalysis in the dearomative Michael addition involving nitro-group-activated benzofurans

The manuscript presents supramolecular catalysis with a cinchona-based squaramide and an acidic co-catalyst. The self-assembly of a well-defined transition state resulted in the formation of relevant heterocycles bearing 3 contiguous stereocenters.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2025-01-01
DOI
https://doi.org/10.1039/d5qo00035a
Citations
1
Primary Topic
Chemical Synthesis and Reactions
Type
article
Field-Weighted Citation Impact
0.94
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article

Supramolecular catalysis in the dearomative Michael addition involving nitro-group-activated benzofurans

Łukasz Albrecht, Anna Skrzyńska, Aleksandra Topolska, Artur Przydacz
1 citations
Organic Chemistry Frontiers
Chemical Synthesis and Reactions
0.94
article

Supramolecular catalysis in the dearomative Michael addition involving nitro-group-activated benzofurans

Łukasz Albrecht, Anna Skrzyńska, Aleksandra Topolska, Artur Przydacz
article en
1 citations

Abstract

The manuscript presents supramolecular catalysis with a cinchona-based squaramide and an acidic co-catalyst. The self-assembly of a well-defined transition state resulted in the formation of relevant heterocycles bearing 3 contiguous stereocenters.

Organic Chemistry FrontiersVol. 12(11)
Lodz University of Technology (PL), Institute of Organic Chemistry (PL)
Openalex Percentile: Top 28%
Chemical Synthesis and Reactions
0.94
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