| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5142337 | Arabian Journal of Chemistry | 2017 | 9 Pages |
Abstract
Reaction of 2,2-dimethyl-1,3-dioxane-4,6-dione (Meldrum's acid) with various aldehydes in the presence of cyanogen bromide and triethylamine leads to the selective and efficient formation of full-substituted cyclopropanes at room temperature. The products were obtained in good to excellent yields. Structure elucidation is carried out by 1H, 13C NMR, FT-IR spectroscopy and mass analysis techniques. A possible mechanism for the formation is discussed.
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Authors
Nader Noroozi Pesyan, Ali Gharib, Mohammad Behroozi, Alireza Shokr,