Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5270018 | Tetrahedron Letters | 2014 | 11 Pages |
Abstract
The trichloroacetamidine intermediates, generated by addition of benzylamine derivatives to trichloroacetonitrile, react with the Knoevenagel condensation product of ninhydrin and malononitrile to afford trichloromethylated [3.3.3]propellanes, in good yields. When benzylamine was used, a plane-symmetrical spiro-compound was obtained.
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Authors
Issa Yavari, Alaleh Malekafzali, Stavroula Skoulika,