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Synthesis of trifluoromethyl-/cyclopropyl-substituted 2-isoxazolines by DBU-promoted domino reaction
Chinese Chemical Letters ( IF 9.4 ) Pub Date : 2017-08-01 , DOI: 10.1016/j.cclet.2017.03.031 Xiao-Dong Liu , Hai-Yan Ma , Chun-Hui Xing , Long Lu
Chinese Chemical Letters ( IF 9.4 ) Pub Date : 2017-08-01 , DOI: 10.1016/j.cclet.2017.03.031 Xiao-Dong Liu , Hai-Yan Ma , Chun-Hui Xing , Long Lu
Abstract NTrifluoromethyl and cyclopropyl substituted 2-isoxazolines were synthesized via a DBU-promoted domino reaction of β-trifluoromethyl-/β-cyclopropyl-substituted enones with hydroxylamine. The domino reaction consists of a Michael addition and the followed cyclization. A wide range of 3-substituted 5-cyclopropyl-5- trifluoromethyl-2-isoxazolines were obtained in good to excellent yields under mild reaction conditions. The method could also apply to other trifluoromethyl-substituted enones.
中文翻译:
DBU促进的多米诺反应合成三氟甲基/环丙基取代的2-异恶唑啉
摘要通过β-三氟甲基-/β-环丙基取代的烯酮与羟胺的DBU促进的多米诺反应,合成了N-三氟甲基和环丙基取代的2-异恶唑啉。多米诺反应由迈克尔加成和随后的环化组成。在温和的反应条件下,以良好或优异的产率获得了广泛的3-取代的5-环丙基-5-三氟甲基-2-异恶唑啉。该方法也可以应用于其他三氟甲基取代的烯酮。
更新日期:2017-08-01
中文翻译:
DBU促进的多米诺反应合成三氟甲基/环丙基取代的2-异恶唑啉
摘要通过β-三氟甲基-/β-环丙基取代的烯酮与羟胺的DBU促进的多米诺反应,合成了N-三氟甲基和环丙基取代的2-异恶唑啉。多米诺反应由迈克尔加成和随后的环化组成。在温和的反应条件下,以良好或优异的产率获得了广泛的3-取代的5-环丙基-5-三氟甲基-2-异恶唑啉。该方法也可以应用于其他三氟甲基取代的烯酮。