Issue 38, 2013

Palladium-catalyzed annulation reactions of methyl o-halobenzoates with azabicyclic alkenes: a general protocol for the construction of benzo[c]phenanthridine derivatives

Abstract

The annulation reaction of methyl o-halobenzoates with azabicyclic alkenes proceeds efficiently to give the corresponding benzo[c]phenanthridine derivatives in good to excellent yields using a developed base-free methodology based on our preliminary studies. Thirty-seven application examples validate the compatibility of the present strategy with different groups, particularly with the electron-deficient ones, that are difficult to access using other traditional methods. In addition, annulation reactions with non-symmetric azabicyclic alkenes are achieved in high regioselectivity.

Graphical abstract: Palladium-catalyzed annulation reactions of methyl o-halobenzoates with azabicyclic alkenes: a general protocol for the construction of benzo[c]phenanthridine derivatives

Supplementary files

Article information

Article type
Paper
Submitted
19 May 2013
Accepted
08 Jul 2013
First published
09 Jul 2013

RSC Adv., 2013,3, 17271-17280

Palladium-catalyzed annulation reactions of methyl o-halobenzoates with azabicyclic alkenes: a general protocol for the construction of benzo[c]phenanthridine derivatives

C. Guo, K. Huang, B. Wang, L. Xie and X. Xu, RSC Adv., 2013, 3, 17271 DOI: 10.1039/C3RA42474J

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