Abstract
N-Aryl- and N-allylimines derived typically from substituted acetophenones undergo palladium(II)-catalyzed dehydrogenative cyclization reactions in the presence of tetrabutylammonium bromide and molecular oxygen in DMSO to afford indole and pyrrole derivatives, respectively, in moderate to good yields. The reactions are operationally simple and can be readily performed on multigram scales (up to 55 mmol).
Original language | English |
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Article number | ss-2014-z0303-psp |
Pages (from-to) | 2727-2733 |
Number of pages | 7 |
Journal | Synthesis |
Volume | 46 |
Issue number | 20 |
DOIs | |
Publication status | Published - 2014 Oct 1 |
Keywords
- C-H activation
- Heck reaction
- imines
- indoles
- palladium
- pyrroles