Srinivasa, G. R. and Abiraj, K. and Chenne Gowda, D. (2004) Facile synthesis of azo compounds from aromatic nitro compounds using magnesium and triethylammonium formate. Australian Journal Of Chemistry, 57 (6). pp. 609-610. ISSN 0004-9425
Full text not available from this repository. (Request a copy)Abstract
Magnesium/triethylammonium formate is a convenient reagent for the reduction of aromatic nitro compounds to corresponding symmetrically substituted azo compounds. Various azo compounds containing additional reducible substituents, including halogen, nitrile, acid, phenol, ester, and methoxy functions, have been synthesized in a single step by the use of this reagent. The conversion is reasonably fast, clean, high yielding, and occurs at room temperature in methanol.
| Item Type: | Article |
|---|---|
| Subjects: | C Chemical Science > Chemistry |
| Divisions: | Department of > Chemistry |
| Depositing User: | Users 23 not found. |
| Date Deposited: | 22 Aug 2019 09:45 |
| Last Modified: | 02 Jul 2022 09:41 |
| URI: | http://eprints.uni-mysore.ac.in/id/eprint/6626 |
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