Publishing: Journals, books and databases
Close Icon
 
Scheduled maintenance upgrade on Thursday, 18th of February from 10am to 12pm (GMT)
Please note that we will be performing a planned maintenance upgrade on Thursday 18th of February from 10am to 12pm Greenwich Mean Time. During this time you may experience an intermittent reduction in performance, with the possibility of our services being offline temporarily on our publishing platform . If you have any questions please use the feedback button on this page. We apologise for any inconvenience this might cause and thank you for your patience.
Urgent high quality communications from across the chemical sciences.
Impact Factor 6.834 100 Issues per Year Indexed in Medline
Communication

Product-selectivity control by the nature of the catalyst: Lewis acid-catalyzed selective formation of ring-fused tetrahydroquinolines and tetrahydroazepines via intramolecular redox reaction

*
Corresponding authors
a
Shanghai Key Laboratory of Green Chemistry and Chemical Processes, Department of Chemistry, East China Normal University, 3663 N. Zhongshan Road, Shanghai 200062, P.R. China
E-mail: jlzhang@chem.ecnu.edu.cn
Fax: (+86) 21-6223-5039
b
State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Road, Shanghai 200032, P.R. China
Chem. Commun., 2010,46, 6593-6595

DOI: 10.1039/C0CC01946A
Received 18 Jun 2010, Accepted 02 Jul 2010
First published online 10 Aug 2010
| | | | | | More
Please wait while Download options loads
 
 

Supplementary Info