Jump to main content
Jump to site search
PLANNED MAINTENANCE Close the message box

Scheduled maintenance work on Wednesday 27th March 2019 from 11:00 AM to 1:00 PM (GMT).

During this time our website performance may be temporarily affected. We apologise for any inconvenience this might cause and thank you for your patience.


Issue 4, 2018
Previous Article Next Article

Enantioselective palladium-catalyzed C–H functionalization of pyrroles using an axially chiral 2,2′-bipyridine ligand

Author affiliations

Abstract

An enantioselective C–H functionalization of pyrrole derivatives with diazo compounds has been successfully realized with up to 90% ee by employing dichlorobis(benzonitrile)palladium with an axially chiral bipyridine ligand C3-ACBP as the catalyst. Asymmetric C–H functionalization at the gram scale was also conducted smoothly with good reactivity and enantioselectivity.

Graphical abstract: Enantioselective palladium-catalyzed C–H functionalization of pyrroles using an axially chiral 2,2′-bipyridine ligand

Back to tab navigation

Supplementary files

Publication details

The article was received on 09 Sep 2017, accepted on 03 Nov 2017 and first published on 06 Nov 2017


Article type: Research Article
DOI: 10.1039/C7QO00815E
Citation: Org. Chem. Front., 2018,5, 611-614

  •   Request permissions

    Enantioselective palladium-catalyzed C–H functionalization of pyrroles using an axially chiral 2,2′-bipyridine ligand

    H. Shen, C. Liu, J. Zhou and Y. Zhou, Org. Chem. Front., 2018, 5, 611
    DOI: 10.1039/C7QO00815E

Search articles by author

Spotlight

Advertisements