A CONVENIENT METHOD FOR THE PREPARATION OF SECONDARY PROPARGYLIC ETHERS - THE REACTION OF ACETALS WITH 1-TRIMETHYLSILYLALKYNES PROMOTED BY THE COMBINED USE OF CATALYTIC AMOUNTS OF TIN(IV) CHLORIDE AND ZINC-CHLORIDE

被引：34

作者：

HAYASHI, M

INUBUSHI, A

MUKAIYAMA, T

机构：

来源：

CHEMISTRY LETTERS | 1987年 / 10期

关键词：

D O I：

10.1246/cl.1987.1975

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

收藏

页码：1975 / 1978

页数：4

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[1] AN ESSENTIALLY MILD AND EFFICIENT CATALYST SYSTEM FOR THE ACTIVATION OF CARBONYL-COMPOUNDS AND THEIR DERIVATIVES - THE COMBINED USE OF TRIMETHYLSILYL CHLORIDE AND TIN(II) CHLORIDE [J].

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CHEMISTRY LETTERS, 1987, (03) :463-466

[2] ASYMMETRIC-SYNTHESIS VIA ACETAL TEMPLATES .4. REACTIONS WITH SILYLACETYLENIC COMPOUNDS - FORMATION OF CHIRAL PROPARGYLIC ALCOHOLS [J].

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[4] AN EFFICIENT AND EXTREMELY MILD CATALYST SYSTEM, COMBINED USE OF TRITYL CHLORIDE AND TIN(II) CHLORIDE, IN THE ALDOL AND MICHAEL REACTIONS [J].

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[6] TITANIUM TETRACHLORIDE IN ORGANIC-SYNTHESIS [J].

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[7] A FACILE SYNTHESIS OF HOMOALLYL ETHERS - THE REACTION OF ACETALS WITH ALLYLTRIMETHYLSILANES PROMOTED BY TRITYL PERCHLORATE OR DIPHENYLBORYL TRIFLATE [J].

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[8] A FACILE SYNTHESIS OF 1,5-DIENES AND BETA,GAMMA-UNSATURATED NITRILES VIA TRITYL PERCHLORATE-CATALYZED ALLYLATION [J].

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CHEMISTRY LETTERS, 1987, (06) :1167-1170