ZINC IODIDE CATALYZED REACTION OF OXETANES WITH TRIMETHYLSILYL CYANIDE

被引：8

作者：

CARR, SA ^{[1
]}

WEBER, WP ^{[1
]}

机构：

[1] UNIV SO CALIF,DEPT CHEM,LOKER HYDROCARBON RES INST,LOS ANGELES,CA 90089

来源：

SYNTHETIC COMMUNICATIONS | 1985年 / 15卷 / 09期

关键词：

D O I：

10.1080/00397918508063872

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：775 / 781

页数：7

共 14 条

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[6] OPENING OF EPOXIDES WITH TRIMETHYLSILYL CYANIDE TO PRODUCE BETA-HYDROXY ISONITRILES - A GENERAL-SYNTHESIS OF OXAZOLINES AND BETA-AMINO ALCOHOLS [J].

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[7] DIRECTIVE EFFECTS IN THE OPENING OF EPOXIDES WITH TRIMETHYLSILYL CYANIDE ZINC IODIDE - THE ESTABLISHMENT OF 3 CONTIGUOUS CHIRAL CENTERS [J].

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[8]

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[9] REGIOSPECIFICITY OF REACTIONS OF EPOXIDES AND OXETANES WITH TRIMETHYLSILYL CYANIDE [J].

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WEBER, WP .

JOURNAL OF ORGANIC CHEMISTRY, 1982, 47 (15) :2873-2875

[10] REACTION OF DIMETHYLOXOSULFONIUM METHYLIDE WITH EPOXIDES - PREPARATION OF OXETANES [J].

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