Enantioselective intramolecular benzylic C-H bond amination: efficient synthesis of optically active benzosultams.

Angew Chem Int Ed Engl

Department of Chemistry, Faculty of Science Graduate School, Kyushu University, Hakozaki, Higashi-ku, Fukuoka, Japan.

Published: October 2011

'Salen' along: the iridium(III)-salen complex 1 efficiently catalyzes the title reaction of 2-ethylbenzenesulfonyl azides to give five-membered sultams with high enantioselectivity. Other 2-alkyl-substitued substrates lead to five- and six-membered sultams with high enantioselectivity; the regioselectivity depends upon the substrate and the catalyst used. EDG=electron-donating group.

Download full-text PDF

Source
http://dx.doi.org/10.1002/anie.201101801DOI Listing

Publication Analysis

Top Keywords

sultams high
8
high enantioselectivity
8
enantioselective intramolecular
4
intramolecular benzylic
4
benzylic c-h
4
c-h bond
4
bond amination
4
amination efficient
4
efficient synthesis
4
synthesis optically
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!