Affiliation:
1. Leibniz Universität Hannover, Institut für Organische Chemie
2. Quaid-I-Azam University, Department of Chemistry
3. Helmholtz Zentrum für Infektionsforschung (HZI)
Abstract
AbstractThe Diels–Alder reaction has long been established as an extremely useful procedure in the toolbox of natural product chemists. It tolerates a wide spectrum of building blocks of different complexity and degrees of derivatization, and enables the formation of six-membered rings with well-defined stereochemistry. In recent years, many total syntheses of natural products have been reported that rely, at some point, on the use of a [4+2]-cycloaddition step. Among classic approaches, several modifications of the Diels–Alder reaction, such as hetero-Diels–Alder reactions, dehydro-Diels–Alder reactions and domino-Diels–Alder reactions, have been employed to extend the scope of this process in the synthesis of natural products. Our short review covers applications of the Diels–Alder reaction in natural product syntheses between 2017 and 2020, as well as selected methodologies which are inspired by, or that can be used to access natural products.1 Introduction2 Syntheses from 20173 Syntheses from 20184 Syntheses from 20195 Syntheses from 20206 Conclusion
Funder
Alexander von Humboldt Foundation
Subject
Organic Chemistry,Catalysis
Cited by
14 articles.
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