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Convenient synthesis of (4R,5R)-4,5-bis(aminomethyl)-2-isopropyl- 1,3-dioxolane
引用本文:Jian Jiang De Cai Wang Wei Lin Ping Kai Ouyang. Convenient synthesis of (4R,5R)-4,5-bis(aminomethyl)-2-isopropyl- 1,3-dioxolane[J]. 中国化学快报, 2007, 18(7): 783-784. DOI: 10.1016/j.cclet.2007.05.035
作者姓名:Jian Jiang De Cai Wang Wei Lin Ping Kai Ouyang
作者单位:Jian Jiang,De Cai Wang *,Wei Lin,Ping Kai Ouyang College of Life Science and Pharmaceutical Engineering,Nanjing University of Technology,Nanjing 210009,China
摘    要:A convenient approach for the preparation of (4R,5R)-4,5-bis(aminomethyl)-2-isopropyl-1,3-dioxolane is described. The target compound via two steps is synthesized from diethyl-2,3-O-isobutylidene-D-tartrate, through ammonolysis and reduction.

关 键 词:合成 抗癌药物 氨甲基 中间体 二恶茂烷
收稿时间:2007-02-26
修稿时间:2007-02-26

Convenient synthesis of (4R,5R)-4,5-bis(aminomethyl)-2-isopropyl- 1,3-dioxolane
Jian Jiang,De Cai Wang,Wei Lin,Ping Kai Ouyang. Convenient synthesis of (4R,5R)-4,5-bis(aminomethyl)-2-isopropyl- 1,3-dioxolane[J]. Chinese Chemical Letters, 2007, 18(7): 783-784. DOI: 10.1016/j.cclet.2007.05.035
Authors:Jian Jiang  De Cai Wang  Wei Lin  Ping Kai Ouyang
Affiliation:College of Life Science and Pharmaceutical Engineering, Nanjing University of Technology, Nanjing 210009, China
Abstract:A convenient approach for the preparation of (4R,5R)-4,5-bis(aminomethyl)-2-isopropyl-1,3-dioxolane is described. The target compound via two steps is synthesized from diethyl-2,3-O-isobutylidene-D-tartrate, through ammonolysis and reduction.
Keywords:Heptaplatin  Aminomethyl  Intermediate  Anticancer drug
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