A novel reductive ring-opening reaction of isoxazolidine to form functionalized 1, 3-aminoalcohol

Hong Kui Zhang Wing Hong Chan Albert W. M. Lee Ping Fang Xia Wai Yeung Wong

引用本文: Hong Kui Zhang,  Wing Hong Chan,  Albert W. M. Lee,  Ping Fang Xia,  Wai Yeung Wong. A novel reductive ring-opening reaction of isoxazolidine to form functionalized 1, 3-aminoalcohol[J]. Chinese Chemical Letters, 2007, 18(6): 629-632. doi: 10.1016/j.cclet.2007.04.001 shu
Citation:  Hong Kui Zhang,  Wing Hong Chan,  Albert W. M. Lee,  Ping Fang Xia,  Wai Yeung Wong. A novel reductive ring-opening reaction of isoxazolidine to form functionalized 1, 3-aminoalcohol[J]. Chinese Chemical Letters, 2007, 18(6): 629-632. doi: 10.1016/j.cclet.2007.04.001 shu

A novel reductive ring-opening reaction of isoxazolidine to form functionalized 1, 3-aminoalcohol

摘要: Reductive cleavage of the N-O bond of isoxazolidine ring with catalytic hydrogenation over Raney nickel was described.Bicyclic isoxazolidines could be effectively converted into the corresponding 1, 3-amino-alcohol possessing a sultone or sultam moiety with high conversion and yield when the hydrogenation was catalyzed by freshly prepared Raney nickel under a pressure of 40 psi in the presence of triethylamine.

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  • 收稿日期:  2006-11-13
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