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A second-generation ligand for the enantioselective rhodium-catalyzed addition of arylboronic acids to alkenylazaarenes

Roy, Iain D.; Burns, Alan R.; Pattison, Graham; Michel, Boris; Parker, Alexandra J.; Lam, Hon Wai

Authors

Iain D. Roy

Alan R. Burns

Graham Pattison

Boris Michel

Alexandra J. Parker

HON LAM Hon.Lam@nottingham.ac.uk
Professor of Sustainable Chemistry



Abstract

A 2,4,6-trialkylanilide-containing chiral diene has been identified as a superior ligand for the enantioselective rhodiumcatalyzed arylation of alkenylazaarenes with arylboronic acids.

Citation

Roy, I. D., Burns, A. R., Pattison, G., Michel, B., Parker, A. J., & Lam, H. W. (2014). A second-generation ligand for the enantioselective rhodium-catalyzed addition of arylboronic acids to alkenylazaarenes. Chemical Communications, 50(22), https://doi.org/10.1039/C4CC00340C

Journal Article Type Article
Acceptance Date Jan 24, 2014
Online Publication Date Feb 3, 2014
Publication Date Mar 18, 2014
Deposit Date Jun 9, 2017
Publicly Available Date Jun 9, 2017
Journal Chemical Communications
Print ISSN 1359-7345
Electronic ISSN 1364-548X
Publisher Royal Society of Chemistry
Peer Reviewed Peer Reviewed
Volume 50
Issue 22
DOI https://doi.org/10.1039/C4CC00340C
Public URL http://eprints.nottingham.ac.uk/id/eprint/43481
Publisher URL http://pubs.rsc.org/en/Content/ArticleLanding/2014/CC/C4CC00340C#!divAbstract
Copyright Statement Copyright information regarding this work can be found at the following address: http://eprints.nottingham.ac.uk/end_user_agreement.pdf

Files


HON2 Arylation of alkenylazaarenes Chem Commun submission 2.pdf (1.1 Mb)
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Copyright Statement
Copyright information regarding this work can be found at the following address: http://eprints.nottingham.ac.uk/end_user_agreement.pdf





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