Literature DB >> 35555954

Synthesis of W-Phos Ligand and Its Application in the Copper-Catalyzed Enantioselective Addition of Linear Grignard Reagents to Ketones.

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.
© 2022 Wiley-VCH GmbH.

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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


  1 in total

1.  Ligand-dependent, palladium-catalyzed stereodivergent synthesis of chiral tetrahydroquinolines.

Authors:  Yue Wang; Er-Qing Li; Zheng Duan
Journal:  Chem Sci       Date:  2022-06-20       Impact factor: 9.969

  1 in total

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