Published August 13, 2003
| Supplemental Material
Journal Article
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Catalytic C−H Bond Functionalization with Palladium(II): Aerobic Oxidative Annulations of Indoles
- Creators
- Ferreira, Eric M.
- Stoltz, Brian M.
Abstract
A palladium-catalyzed aerobic oxidative annulation of indoles is described. We have demonstrated that a variety of factors influence these cyclizations, and in particular the electronic nature of the pyridine ligand is crucial. It is also remarkable that these oxidative cyclizations can proceed in good yield despite background oxidative decomposition pathways, testament to the facile nature with which molecular oxygen can serve as the direct oxidant for Pd(0). We have also shown that the mechanism most likely involves initial indole palladation (formal C−H bond activation) followed by migratory insertion and β-hydrogen elimination.
Additional Information
© 2003 American Chemical Society. Received 7 March 2003. Published online 22 July 2003. Published in print 1 August 2003. We thank the NIH-NIGMS (GM65961-01) and the NSF (predoctoral fellowship to E.M.F.) for generous financial support, and Professors András Kotschy and Greg Fu for stimulating discussions.Attached Files
Supplemental Material - ja035054ysi20030620_120442.pd
Supplemental Material - ja035054ysi20030620_120442.pdf
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Additional details
- Eprint ID
- 74363
- DOI
- 10.1021/ja035054y
- Resolver ID
- CaltechAUTHORS:20170216-082726177
- GM65961-01
- NIH
- NSF Predoctoral Fellowship
- Created
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2017-02-16Created from EPrint's datestamp field
- Updated
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2021-11-11Created from EPrint's last_modified field