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Making Chiral Salen Complexes Work with Organocatalysts

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CHEMICAL REVIEWS
卷 122, 期 9, 页码 8841-8883

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AMER CHEMICAL SOC
DOI: 10.1021/acs.chemrev.1c00912

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  1. Universite Paris Saclay
  2. CNRS
  3. Charm3At LabEx [ANR-11-LABEX-0039]

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In this article, the applications of bisimine derivatives of salicylaldehyde with chiral diamines (salens) in asymmetric organometallic catalysis are reviewed and classified according to the organocatalyst. The mechanisms and physical-organic chemistry considerations of these complex catalytic systems are discussed for a better understanding.
Bisimine derivatives of salicylaldehyde with chiral diamines (salens) are privileged ligands in asymmetric organometallic catalysis, which can be used in cooperation with organocatalysts as additives. The latter can be a modifier of the metal reactivity by liganding or a true co-catalyst working in tandem or in a dual system. All scenarios encountered in the literature are reviewed and classified according to the organocatalyst. In each case, mechanistic and physical-organic chemistry considerations are discussed to better understand the gears of these complex catalytic settings.

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