Diels–Alder Reactions of 1,2-Dihydropyridines: An Efficient Tool for the Synthesis of Isoquinuclidines

Author:

Silva Eduarda12,Silva Artur2ORCID,Rocha Djenisa2

Affiliation:

1. LAQV, REQUIMTE, Department of Chemistry Sciences, Faculty of Pharmacy, University of Porto

2. QOPNA, Department of Chemistry, University of Aveiro

Abstract

The Diels–Alder reaction of 1,2-dihydropyridines with different dienophiles is a well-established and straightforward method for the synthesis of isoquinuclidines. Nevertheless, the enantioselective preparation of isoquinuclidines using organocatalysts or organometallic catalysts is rather unexplored. This succinct review offers readers an overall perspective of the most important recent developments and concepts related to this topic.1 Introduction2 Asymmetric Diels–Alder Reaction of 1,2-Dihydropyridines2.1 Transition-Metal-Catalyzed Reactions2.2 Organocatalyzed Reactions3 Diels–Alder Reaction of 1,2-Dihydropyridines in the Synthesis of Biologically Valuable Compounds4 Conclusion

Funder

FEDER - Operational Competitiveness and Internationalization Program

Fundação para a Ciência e a Tecnologia

Publisher

Georg Thieme Verlag KG

Subject

Organic Chemistry,Catalysis

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