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DOI: 10.1055/a-1771-0641
Stereoselective Domino Reactions in the Synthesis of Spiro Compounds
M.B. thanks Ministero dell’Istruzione, dell’Università e della Ricerca (MUR) for the project PRIN 2017 NATURECHEM. F.M. also thanks MUR project PRIN 2017 NATURECHEM for a postdoctoral fellowship. S.J.G. thanks Conselho Nacional de Desenvolvimento Científico e Tecnológico for financial support.
Abstract
This review summarizes the latest developments in asymmetric domino reactions, with the emphasis on the preparation of spiro compounds. Discussions on the stereoselectivity of the transformations, the reaction mechanisms, the rationalization of the stereochemical outcome, and the applications of domino reactions to the synthesis of biologically active molecules and natural products are included when appropriate.
1 Introduction
2 Asymmetric Domino Reactions
2.1 Domino Reactions Initiated by Michael Reactions
2.2 Domino Reactions Initiated by Mannich Reactions
2.3 Domino Reactions Initiated by Knoevenagel Reactions
2.4 Domino Reactions Initiated by Cycloaddition Reactions
2.5 Domino Reactions Initiated by Metal Insertion
2.6 Other Mechanisms
3 Conclusion
Key words
domino reactions - spiro compounds - stereoselective synthesis - organocatalysis - natural productsPublication History
Received: 20 December 2021
Accepted after revision: 14 February 2022
Accepted Manuscript online:
14 February 2022
Article published online:
16 May 2022
© 2022. Thieme. All rights reserved
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For reviews, see:
For review, see:
Reviews:
For selected examples of biologicaly active pyrrolin-4-ones see:
For review see:
For review see: