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Synthesis 2020; 52(06): 781-795
DOI: 10.1055/s-0039-1690044
DOI: 10.1055/s-0039-1690044
review
Recent Developments in Highly Stereoselective Michael Addition Reactions Catalyzed by Metal Complexes
We gratefully acknowledge the financial support of the Russian Science Foundation (grant No. 18-13-00447).Weitere Informationen
Publikationsverlauf
Received: 05. November 2019
Accepted after revision: 09. Dezember 2019
Publikationsdatum:
03. Januar 2020 (online)
Abstract
Achieving high enantioselectivity and diastereoselectivity simultaneously is a rather challenging task for asymmetric catalytic synthesis. Thanks to the rapid development of asymmetric transition-metal catalysis, significant progress has been made during recent years in achieving highly enantio- and diastereoselective conjugate addition reactions with a diverse combination of Michael donors and acceptors. This short review surveys the advances in transition-metal-catalyzed asymmetric diastereoselective Michael addition including diastereodivergent catalysis developed between 2015 and 2019. The review is divided into multiple parts according to the type of nucleophiles involved in the reaction.
1 Introduction
2 Addition of Functionalized Ketones and Dicarbonyl Compounds
3 Addition of Aldimino Esters and Their Cyclic Analogues
4 Addition of Indolin-2-ones
5 Vinylogous Michael Reactions
6 Other Michael Donors
7 Cascade Reactions Initiated by Michael Addition
8 Conclusion
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