First total synthesis of macrosphelides C and F

被引:28
作者
Kobayashi, Y [1 ]
Acharya, HP [1 ]
机构
[1] Tokyo Inst Technol, Dept Biomol Engn, Midori Ku, Yokohama, Kanagawa 2268501, Japan
关键词
asymmetric synthesis; furans; macrolides; macrosphelide C; macrosphelide F;
D O I
10.1016/S0040-4039(01)00285-4
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Macrosphelides C and F were synthesized by lactonization of 14-oxo seco acids at the O(10)-C(11) bond followed by reduction and Mitsunobu inversion of the resulting hydroxyl group. The seco acids were prepared from the corresponding furans by furan ring-opening with NBS followed by further oxidation of the 4-oxo-2-alkenals with NaClO2. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:2817 / 2820
页数:4
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