Literature DB >> 27006303

New biphenyl iminium salt catalysts for highly enantioselective asymmetric epoxidation: role of additional substitution and dihedral angle.

Philip C Bulman Page1, Christopher J Bartlett1, Yohan Chan1, Steven M Allin2, Michael J McKenzie3, Jérôme Lacour4, Garth A Jones1.   

Abstract

New biaryl iminium salt catalysts for enantioselective alkene epoxidation containing additional substitution in the heterocyclic ring are reported. The effects upon conformation and enantioselectivity of this additional substitution, and the influence of dihedral angle in these systems, has been investigated using a synthetic approach supported by density functional theory. Enantioselectivities of up to 97% ee were observed.

Entities:  

Year:  2016        PMID: 27006303     DOI: 10.1039/c6ob00542j

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  2 in total

1.  A Highly Efficient Heterogeneous Catalyst of Bimetal-Organic Frameworks for the Epoxidation of Olefin with H2O2.

Authors:  Fei Wang; Xiang-Guang Meng; Yan-Yan Wu; Hong Huang; Jing Lv; Wen-Wang Yu
Journal:  Molecules       Date:  2020-05-21       Impact factor: 4.411

2.  Organocatalytic Enantioselective Synthesis of Bicyclo[2.2.2]octenones via Oxaziridinium Catalysed ortho-Hydroxylative Phenol Dearomatization.

Authors:  Tom D D'Arcy; Mark R J Elsegood; Benjamin R Buckley
Journal:  Angew Chem Int Ed Engl       Date:  2022-06-10       Impact factor: 16.823

  2 in total

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