| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10575605 | Journal of Organometallic Chemistry | 2005 | 5 Pages |
Abstract
The Pauson-Khand reaction of 2-ethynyl aniline gives the expected cyclopentenone product, with the aniline alpha to the ketone. Treatment with organocuprates gives not the simple conjugate addition product, but the indole derived from an addition-cyclisation-nucleophilic attack sequence.
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Michael P. Coogan, Li-ling Ooi, Derek S. Wilkins,