2.11 Iron-Based Chiral Lewis Acid Catalysts in Organic Synthesis
Book
Editor: Yoshikai, N.
Title: Base-Metal Catalysis 2
Print ISBN: 9783132455030; Online ISBN: 9783132455054; Book DOI: 10.1055/b000000440
1st edition © 2023 Thieme. All rights reserved.
Georg Thieme Verlag KG, Stuttgart
Subjects: Organic Chemistry;Chemical Reactions, Catalysis;Organometallic Chemistry;Laboratory Techniques, Stoichiometry
Science of Synthesis Reference Libraries
Parent publication
Title: Science of Synthesis
DOI: 10.1055/b-00000101
Series Editors: Fürstner, A. (Editor-in-Chief); Carreira, E. M.; Faul, M.; Kobayashi, S.; Koch, G.; Molander, G. A.; Nevado, C.; Trost, B. M.; You, S.-L.
Type: Multivolume Edition
Abstract

Various synthetic applications of iron-based Lewis acid complexes are presented through their most noteworthy and groundbreaking applications in asymmetric catalysis. The iron Lewis acids are organized according to their structure, and then their reactivity. It has been reported that various chiral iron Lewis acids can be used in a broad range of synthetic transformations. Diverse categories of chiral ligands are used in asymmetric catalysis using chiral iron complexes, including N,N′-dioxides, bipyridines, oxazolines, Schiff bases, salen/salan-type structures, and aminopyridines.
Key words
base-metal catalysis - iron catalysis - asymmetric catalysis - chiral Lewis acids - chiral iron complexes - chiral ligands- 40 Ge L, Zhou H, Chiou M.-F, Jiang H, Jian W, Ye C, Li X, Zhu X, Xiong H, Li Y, Song L, Zhang X, Bao H. Nat. Catal. 2021; 4: 28
- 60 Chen K.-G, Lu H, Zhou Y.-M, Wan X.-L, Wang H.-Y, Xu Z.-J, Guo H.-M, Che C.-M. J. Org. Chem. 2022; 87: 8289