REGIOSELECTIVE RING-OPENING OF SILYL EPOXY ALCOHOLS WITH AZIDE ION

被引：27

作者：

CHAKRABORTY, TK

REDDY, GV

机构：

[1] Indian Institute of Chemical Technology, Hyderabad

来源：

TETRAHEDRON LETTERS | 1990年 / 31卷 / 09期

关键词：

D O I：

10.1016/S0040-4039(00)88800-0

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：1335 / 1338

页数：4

共 22 条

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[4] SELECTIVE TRANSFORMATIONS OF 2,3-EPOXY ALCOHOLS AND RELATED DERIVATIVES - STRATEGIES FOR NUCLEOPHILIC-ATTACK AT CARBON-3 OR CARBON-2
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[5] REGIOSELECTIVE AZIDE OPENING OF 2,3-EPOXY ALCOHOLS BY [TI(O-I-PR)2(N3)2] - SYNTHESIS OF ALPHA-AMINO-ACIDS
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[6] TI(O-I-PR)4-MEDIATED NUCLEOPHILIC OPENINGS OF 2,3-EPOXY ALCOHOLS - A MILD PROCEDURE FOR REGIOSELECTIVE RING-OPENING
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[J]. JOURNAL OF ORGANIC CHEMISTRY, 1985, 50 (09) : 1557 - 1560
[7] Colvin E. W., 1988, SILICON REAGENTS ORG
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[10] REACTIONS OF ALPHA,BETA-EPOXYSILANES WITH ORGANOCUPRATE REAGENTS - NEW STEREOSPECIFIC OLEFIN SYNTHESIS
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