Chandrasekhar, Sosale and Murthy, Tara (1987) Nucleophilic Addition to $\alpha$, $\alpha$-Dihalogenocarbonyl Compounds: Synthetic and Mechanistic Implications. In: Journal of Chemical Research, Synopses (12). pp. 414-415.
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Hydride reduction of dibromoketones $RCOCHBr_2$ $(R=Ph, CMe_3)$ gave $RCH(OH)CHBr_2$, which, when treated with KOH in $CCl_4$, gave aldehydes RCHBrCHO via intermediate bromoepoxides I. Grignard dialkylation of $Cl_2CHCOCl$ gave chloroalcs. $Cl_2CHCR_{12}OH$ $(II, R_1=Me, Ph, PhCH_2)$ in 85-96% yields. Similar rearrangement of II with KOH in $CCl_4$ gave the corresponding chloroaldehydes $R_{12}CClCHO$.
| Item Type: | Journal Article |
|---|---|
| Additional Information: | Copyright of this article belongs to Royal Society of Chemistry. |
| Department/Centre: | Division of Chemical Sciences > Organic Chemistry |
| Date Deposited: | 28 Apr 2008 |
| Last Modified: | 27 Aug 2008 13:20 |
| URI: | http://eprints.iisc.ernet.in/id/eprint/13790 |
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