Yadav, J. S. ; Subba Reddy, B. V. ; Narasimhulu, G. ; Chandrakanth, D. ; Satheesh, G. (2009) Cerium(III) chloride heptahydrate-lithium iodide: a novel reagent system for the synthesis of N-arylpyrrolidines Synthesis, 2009 (20). pp. 3443-3448. ISSN 0039-7881
Full text not available from this repository.
Official URL: http://www.thieme-connect.com/ejournals/abstract/s...
Related URL: http://dx.doi.org/10.1055/s-0029-1216970
Abstract
Aldimines, generated in situ from arylamines and aryl aldehydes, undergo smooth cycloaddition with cyclopropane-1,1-dicarboxylate in the presence of the cerium(III) chloride heptahydrate-lithium iodide reagent system in refluxing acetonitrile under neutral conditions to produce the corresponding N-arylpyrrolidines in good yields with high selectivity.
Item Type: | Article |
---|---|
Source: | Copyright of this article belongs to Thieme Medical Publishers. |
Keywords: | Cerium(III) Reagents; Aldimines; Cyclopropanedicarboxylate; Pyrrolidines; Cycloadditions; Ring Expansion |
ID Code: | 63087 |
Deposited On: | 28 Sep 2011 03:40 |
Last Modified: | 28 Sep 2011 03:40 |
Repository Staff Only: item control page