Allen(oat)e transformations catalyzed by isothioureas
Allen(oat)e transformations catalyzed by isothioureas
Matching Funds - Oberösterreich
Disciplines
Chemistry (100%)
Keywords
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Organocatalysis,
Cyclizations,
Method Development,
Asymmetric Catalysis,
Allenoates
Allenoates represent a class of easily accessible and highly reactive small compounds that allow for unique reactions in the presence of different catalysts. The hereby accessible products show high degrees of complexity and are of interest for the syntheses of advanced targets with interesting biological properties, i.e. with respect to potential medical applications. Within this project we wish to establish well-known isothioureas as catalysts for reactions of allenoates, a strategy that has so far not been reported. Preliminary investigations have shown that these catalysts hold much potential to obtain novel products that are not accessible with existing strategies and we will investigate this in detail within this project. The overall goal will therefore be the development of novel unprecedented synthesis methods that provide efficient entries towards complex molecules. Mario Waser 1
- Universität Linz - 100%
- Johanna Novacek, Universität Linz , national collaboration partner
- Markus Himmelsbach, Universität Linz , national collaboration partner
- Matthias Bechmann, Universität Linz , national collaboration partner
- Uwe Monkowius, Universität Linz , national collaboration partner
Research Output
- 6 Publications
- 2 Datasets & models
- 3 Scientific Awards
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2025
Title Asymmetric isochalcogenourea-catalysed (4 + 2)-cycloadditions of ortho-quinone methides and allenoates. DOI 10.1039/d4ob01855a Type Journal Article Author Gross C Journal Organic & biomolecular chemistry Pages 827-834 -
2025
Title Determination of the p K aH of Established Isothiourea Catalysts DOI 10.1002/ejoc.202401412 Type Journal Article Author Bechmann M Journal European Journal of Organic Chemistry -
2024
Title Isochalcogenourea-catalyzed asymmetric (4 + 2)-heterocycloadditions of allenoates. DOI 10.1093/chemle/upae168 Type Journal Article Author Waser M Journal Chemistry letters -
2024
Title Enantioselective Syntheses of 3,4-Dihydropyrans Employing Isochalcogenourea-Catalyzed Formal (4+2)-Cycloadditions of Allenoates. DOI 10.1002/adsc.202400038 Type Journal Article Author Hofer M Journal Advanced synthesis & catalysis Pages 2115-2122 -
2024
Title Chiral Isochalcogenourea-Catalysed Enantioselective (4+2) Cycloadditions of Allenoates. DOI 10.1002/ange.202315345 Type Journal Article Author Mayer P Journal Angewandte Chemie (Weinheim an der Bergstrasse, Germany) -
2024
Title Chiral Isochalcogenourea-Catalysed Enantioselective (4+2) Cycloadditions of Allenoates. DOI 10.1002/anie.202315345 Type Journal Article Author Mayer P Journal Angewandte Chemie (International ed. in English)
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2024
Link
Title CCDC 2324831: Experimental Crystal Structure Determination DOI 10.5517/ccdc.csd.cc2j15kb Type Database/Collection of data Public Access Link Link -
2023
Link
Title CCDC 2297199: Experimental Crystal Structure Determination DOI 10.5517/ccdc.csd.cc2h3f68 Type Database/Collection of data Public Access Link Link
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2025
Title Plenary Lecture Type Personally asked as a key note speaker to a conference Level of Recognition Regional (any country) -
2024
Title ZinShen Lecture at Hangzhou Normal University, China Type Personally asked as a key note speaker to a conference Level of Recognition Continental/International -
2024
Title Angewandte Advances Lecture Type Personally asked as a key note speaker to a conference Level of Recognition Continental/International