Jump to main content
Jump to site search

Issue 95, 2019
Previous Article Next Article

Enantioselective palladium-catalyzed diarylation of unactivated alkenes

Author affiliations

Abstract

Enantioselective Pd-catalyzed diarylation of unactivated alkenes between arenediazonium salts and arylboronic acids has been developed. This method provides an efficient route to dihydrobenzofurans with all-carbon quaternary centers in good yields with 88–99% ee. This reaction proceeding under mild and open-flask conditions is compatible with a variety of functional groups, including cyano, ketone, ester, amide, bromine and free hydroxyl groups.

Graphical abstract: Enantioselective palladium-catalyzed diarylation of unactivated alkenes

Back to tab navigation

Supplementary files

Article information


Submitted
09 Sep 2019
Accepted
01 Nov 2019
First published
01 Nov 2019

Chem. Commun., 2019,55, 14311-14314
Article type
Communication

Enantioselective palladium-catalyzed diarylation of unactivated alkenes

B. Ju, S. Chen and W. Kong, Chem. Commun., 2019, 55, 14311
DOI: 10.1039/C9CC07036B

Social activity

Search articles by author

Spotlight

Advertisements