硝酮
化學性質
編輯硝酮是1,3-偶極體,可發生1,3-偶極環加成反應。它與烯烴發生環加成得到異噁唑啉環系:
這類反應的一個典型例子是Baylis-Hillman加成物與 C-苯基-N-甲基硝酮(R1 = 苯基,R2 = 氫,R3 = 甲基)加成為異噁唑啉的反應。[1]
硝酮也可與末端炔烴在銅鹽存在下反應生成 β-內酰胺,即Kinugasa反應。[2] 例如:[3]
參考資料
編輯- ^ Branislav Dugovič, Lubor Fišera, Christian Hametner and Nada Prónayovác. Diastereoselectivity of Nitrone 1,3-Dipolar Cycloaddition to Baylis-Hillman Adducts. Arkivoc. 2004,. BS-834A [2009-09-22]. (原始內容存檔於2007-09-27).
- ^ Manabu Kinugasa and Shizunobu Hashimoto. The reactions of copper(I) phenylacetylide with nitrones. J. Chem. Soc., Chem. Commun. 1972: 466–467. doi:10.1039/C39720000466.
- ^ Runa Pal and Amit Basak. A novel synthesis of -lactam fused cyclic enediynes by intramolecular Kinugasa reaction. Chem. Commun. 2006: 2992–2994. doi:10.1039/b605743h.