REGIOSELECTIVE RING-OPENING REACTIONS OF 2,3-EPOXY ALCOHOLS WITH SODIUM-AZIDE SUPPORTED ON ZEOLITE CAY

被引：42

作者：

ONAKA, M

SUGITA, K

IZUMI, Y

机构：

来源：

CHEMISTRY LETTERS | 1986年 / 08期

关键词：

D O I：

10.1246/cl.1986.1327

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：1327 / 1328

页数：2

共 8 条

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[2]

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[7] A HIGHLY REGIOSELECTIVE AND STEREOSELECTIVE RING-OPENING OF 2,3-EPOXY ALCOHOLS WITH TRIMETHYLSILYL AZIDE-DIETHYLALUMINUM FLUORIDE SYSTEM [J].

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[8] ASYMMETRIC EPOXIDATION PROVIDES SHORTEST ROUTES TO 4 CHIRAL EPOXY ALCOHOLS WHICH ARE KEY INTERMEDIATES IN SYNTHESES OF METHYMYCIN, ERYTHROMYCIN, LEUKOTRIENE C-1, AND DISPARLURE [J].

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JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1981, 103 (02) :464-465

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