Yadav, J. S. ; Reddy, B. V. S. ; Srinivas, M. ; Sathaiah, K. (2005) Allylation and cyanation of aza-aromatics activated by chloroformate and a catalytic amount of iodine Tetrahedron Letters, 46 (20). pp. 3489-3492. ISSN 0040-4039
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Official URL: http://www.sciencedirect.com/science/article/pii/S...
Related URL: http://dx.doi.org/10.1016/j.tetlet.2005.03.127
Abstract
Allyltrimethylsilane and trimethylsilyl cyanide undergo smooth addition to N-acylated quinolines in the presence of a catalytic amount of iodine to afford 2-allyl- and 2-cyano-1,2-dihydroquinoline derivatives, respectively in good yields with high chemo- and regioselectivity. A variety of functional groups such as alkyl, alkoxy, halo, and nitro functionalities are tolerated under the reaction conditions.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier Science. |
| Keywords: | Aza-aromatics; Iodine Catalysis; Allylation; Cyanation |
| ID Code: | 58916 |
| Deposited On: | 02 Sep 2011 03:21 |
| Last Modified: | 02 Sep 2011 03:21 |
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