Murphy, J.A. and Khan, T.A. and Zhou, S. and Mohan, M. and Thomson, D.W. (2005) Highly efficient reduction of unactivated aryl and alkyl iodides by a ground-state neutral organic electron donor. Angewandte Chemie, 44 (9). pp. 1356-1360. ISSN 1521-3757
Full text not available in this repository. (Request a copy from the Strathclyde author)Official URL: http://dx.doi.org/10.1002/anie.200462038
Abstract
Electron-transfer reductions of unactivated aryl and alkyl iodides with a neutral ground-state organic molecule are reported. The reducing agent 1 is formed in two steps from N-methylbenzimidazole using very simple chemistry, and subsequent treatment of the iodoalkane or -arene with 1 affords cyclized products (see scheme).
| Item type: | Article |
|---|---|
| ID code: | 9884 |
| Notes: | PV: 21365 |
| Keywords: | cyclization, synthetic methods, reduction, radical reactions, electron transfer, Chemistry |
| Subjects: | Science > Chemistry |
| Department: | Faculty of Science > Pure and Applied Chemistry Unknown Department |
| Related URLs: | |
| Depositing user: | Strathprints Administrator |
| Date Deposited: | 14 Nov 2011 11:43 |
| Last modified: | 12 Mar 2012 10:52 |
| URI: | http://strathprints.strath.ac.uk/id/eprint/9884 |
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