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https://hdl.handle.net/10356/97583
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Wei, Ye | en |
dc.contributor.author | Deb, Indubhusan | en |
dc.contributor.author | Yoshikai, Naohiko | en |
dc.date.accessioned | 2013-07-11T08:17:13Z | en |
dc.date.accessioned | 2019-12-06T19:44:18Z | - |
dc.date.available | 2013-07-11T08:17:13Z | en |
dc.date.available | 2019-12-06T19:44:18Z | - |
dc.date.copyright | 2012 | en |
dc.date.issued | 2012 | en |
dc.identifier.citation | Wei, Y., Deb, I., & Yoshikai, N. (2012). Palladium-Catalyzed Aerobic Oxidative Cyclization of N-Aryl Imines: Indole Synthesis from Anilines and Ketones. Journal of the American Chemical Society, 134(22), 9098-9101. | en |
dc.identifier.uri | https://hdl.handle.net/10356/97583 | - |
dc.description.abstract | We report here an operationally simple, palladium-catalyzed cyclization reaction of N-aryl imines, affording indoles via the oxidative linkage of two C–H bonds under mild conditions using molecular oxygen as the sole oxidant. The process allows quick and atom-economical assembly of indole rings from inexpensive and readily available anilines and ketones and tolerates a broad range of functional groups. | en |
dc.language.iso | en | en |
dc.relation.ispartofseries | Journal of the American chemical society | en |
dc.rights | © 2012 American Chemical Society. | en |
dc.title | Palladium-catalyzed aerobic oxidative cyclization of N-aryl imines : indole synthesis from anilines and ketones | en |
dc.type | Journal Article | en |
dc.contributor.school | School of Physical and Mathematical Sciences | en |
dc.identifier.doi | 10.1021/ja3030824 | en |
item.grantfulltext | none | - |
item.fulltext | No Fulltext | - |
Appears in Collections: | SPMS Journal Articles |
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