SYNTHESES OF (+/-)- AND (-)-CIS-TRIKENTRIN-A, (+/-)- AND (-)-TRANS-TRIKENTRIN-A, (+/-)-CIS-TRIKENTRIN-B, (+/-)-TRANS-TRIKENTRIN-B, AND (+/-)-ISO-TRANS-TRIKENTRIN-B
SYNTHESES OF (+/-)- AND (-)-CIS-TRIKENTRIN-A, (+/-)- AND (-)-TRANS-TRIKENTRIN-A, (+/-)-CIS-TRIKENTRIN-B, (+/-)-TRANS-TRIKENTRIN-B, AND (+/-)-ISO-TRANS-TRIKENTRIN-B
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DOI：
10.1016/s0040-4020(01)86755-7
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发表时间：
1990-01-01
期刊：
影响因子：
2.1
通讯作者：
NATSUME, M
中科院分区：
文献类型：
--
作者：
MURATAKE, H;WATANABE, M;NATSUME, M
根据图1中的一般方案，从海洋来源合成了标题吲哚生物碱。关键步骤是制备适当取代的β。-羟基羰基化合物（8b）由7b生成，随后8b与吲哚环化反应生成9b。
Synthesis of the titled indole alkaloids from a marine source was accomplished according to the general scheme in Chart 1. The key steps were preparation of suitably substituted .beta.-hydroxyl carbonyl compounds (8b) from 7b, and the subsequent indole cyclization reaction of 8b to form 9b.