| Literature DB >> 35555954 |
Wenjun Luo1,2, Li-Ming Zhang1, Zhan-Ming Zhang1, Junliang Zhang1,2,3.
Abstract
The asymmetric catalytic addition of linear Grignard reagents to ketones has been a long-standing challenge in organic synthesis. Herein, a novel family of PNP ligands (W-Phos) was designed and applied in copper-catalyzed asymmetric addition of linear Grignard reagents to aryl alkyl ketones, allowing facile access to versatile chiral tertiary alcohols in good to high yields with excellent enantioselectivities (up to 94 % yield, 96 % ee). The process can also be used to synthesize chiral allylic tertiary alcohols from more challenging α,β-unsaturated ketones. Notably, the potential utility of this method is demonstrated in the gram-scale synthesis and modification of various densely functionalized medicinally relevant molecules.Entities:
Keywords: Alcohols; Asymmetric Catalysis; Copper; Grignard Reagents; Ketones
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Year: 2022 PMID: 35555954 DOI: 10.1002/anie.202204443
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 16.823