Literature DB >> 31141384

Highly Enantioselective Synthesis of Chiral Benzhydrols via Manganese Catalyzed Asymmetric Hydrogenation of Unsymmetrical Benzophenones Using an Imidazole-Based Chiral PNN Tridentate Ligand.

Fei Ling1, Huacui Hou1, Jiachen Chen1, Sanfei Nian1, Xiao Yi1, Ze Wang1, Dingguo Song1, Weihui Zhong1.   

Abstract

A series of Mn(I) catalysts containing imidazole-based chiral PNN tridentate ligands with controllable "side arm" groups have been established, enabling the asymmetrical hydrogenation of unsymmetrical benzophenones with outstanding activity (up to 13 000 TON) and excellent enantioselectivity (up to >99% ee). This protocol uses K2CO3 as an industrially desirable base and features a wide substrate scope and functional group tolerance. Moreover, the imine group in the catalyst is crucial for accessing high activities and good enantioselectivities.

Entities:  

Year:  2019        PMID: 31141384     DOI: 10.1021/acs.orglett.9b01056

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Robust and efficient hydrogenation of carbonyl compounds catalysed by mixed donor Mn(I) pincer complexes.

Authors:  Wenjun Yang; Ivan Yu Chernyshov; Robin K A van Schendel; Manuela Weber; Christian Müller; Georgy A Filonenko; Evgeny A Pidko
Journal:  Nat Commun       Date:  2021-01-04       Impact factor: 14.919

2.  Recyclable Mn(I) Catalysts for Base-Free Asymmetric Hydrogenation: Mechanistic, DFT and Catalytic Studies.

Authors:  Harikrishnan Jayaprakash; Peter Coburger; Michael Wörle; Antonio Togni; Hansjorg Grützmacher
Journal:  Chemistry       Date:  2022-07-04       Impact factor: 5.020

  2 in total

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