Preparation and absolute configuration of hexahydroxyter- and octahydroxyquaternapthalene derivatives

被引:38
作者
Tanaka, K
Furuta, T
Fuji, K
Miwa, Y
Taga, T
机构
[1] KYOTO UNIV,INST CHEM RES,UJI,KYOTO 611,JAPAN
[2] KYOTO UNIV,FAC PHARMACEUT SCI,SAKYO KU,KYOTO 606,JAPAN
关键词
D O I
10.1016/0957-4166(96)00270-4
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Oxidative coupling reactions of the stereochemically defined S-tetrahydroxybinaphthalene derivative gave a separable mixture of two diastereomers of the quaternaphthalenes of S, S, S and S, R, S configurations, whose stereostructures were confirmed by an alternative chemical transformation through the temaphthalenes as well as the X-ray structure analysis. The CD spectra of the corresponding diastereomers were indicative of the stereochemistry across the axis. Copyright (C) 1996 Elsevier Science Ltd
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页码:2199 / 2202
页数:4
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