An enantio- and stereocontrolled route to epopromycin B via cinchona alkaloid-catalyzed Baylis-Hillman reaction
An enantio- and stereocontrolled route to epopromycin B via cinchona alkaloid-catalyzed Baylis-Hillman reaction
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DOI：
10.1016/s0040-4039(01)01676-8
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发表时间：
2001-10-29
影响因子：
1.8
通讯作者：
Hatakeyama, S
中科院分区：
文献类型：
--
作者：
Iwabuchi, Y;Sugihara, T;Hatakeyama, S
An enantio- and stereocontrolled route to epopromycin B having the epoxy-beta -aminoketone pharmacophore is developed based on the cinchona alkaloid-catalyzed Baylis-Hillman reaction of N-Fmoc-leucinal. (C) 2001 Elsevier Science Ltd. All rights reserved.
