Tunable thiofumarate stereoselective cycloadditions <i>via</i> aminomefloquine catalysis

Norcamphane dicarboxylic acid ester thioester derivatives are obtained with high enantioselectivity via a formal cycloaddition reaction using amino-mefloquine catalysis.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2025-01-01
DOI
https://doi.org/10.1039/d5qo01014d
Primary Topic
Synthesis and Catalytic Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Tunable thiofumarate stereoselective cycloadditions via aminomefloquine catalysis

Rafał Szabla, Przemysław J. Boratyński, Błażej Dziuk, Anna Spyszkiewicz et al.
Organic Chemistry Frontiers
Synthesis and Catalytic Reactions
article

Tunable thiofumarate stereoselective cycloadditions via aminomefloquine catalysis

Rafał Szabla, Przemysław J. Boratyński, Błażej Dziuk, Anna Spyszkiewicz, Radosław Suchanek, Rafał Kowalczyk, Michał Błauciak
article en

Abstract

Norcamphane dicarboxylic acid ester thioester derivatives are obtained with high enantioselectivity via a formal cycloaddition reaction using amino-mefloquine catalysis.

Organic Chemistry FrontiersVol. 12(19)
Wrocław University of Science and Technology (PL), University of Ostrava (CZ), Wroclaw University of Economics and Business (PL), Institute of Advanced Manufacturing Technology (PL), AGH University of Krakow (PL)
Narodowe Centrum Nauki, Wroclawskie Centrum Sieciowo-Superkomputerowe, Politechnika Wroclawska
Openalex Percentile: Top 86%
Synthesis and Catalytic Reactions
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