Nitration of N-acetyl enamines with acet
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Jacek W. Morzycki; Zenon Łotowski; Monika Stȩpniowska; Agnieszka Gryszkiewicz; A
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Article
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1997
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Elsevier Science
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French
⚖ 432 KB
N-acetyl enamines undergo nitration at the double bond. Products of further nitration and oxidation in an allylic position are also formed. Sterically unhindered enamide, N-acetyl-eholest-2-en-3-amine, yields oxadiazole, as one of the reaction products.