THE ADDITION-REACTION OF ACETALS(ALDEHYDES) TO SIMPLE OLEFINS BY THE USE OF A NEW CATALYST SYSTEM

被引：14

作者：

MUKAIYAMA, T

WARIISHI, K

FURUYA, M

KOBAYASHI, S

机构：

来源：

CHEMISTRY LETTERS | 1989年 / 07期

关键词：

D O I：

10.1246/cl.1989.1277

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：1277 / 1280

页数：4

共 14 条

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[5] A NOVEL METHOD FOR THE PREPARATION OF SYMMETRICAL AND UNSYMMETRICAL ETHERS - TRITYL PERCHLORATE PROMOTED REDUCTION OF CARBONYL-COMPOUNDS WITH TRIETHYLSILANE [J].

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CHEMISTRY LETTERS, 1988, (08) :1291-1294

[8] 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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[9] THE ADDITION-REACTION OF ACETALS TO ACTIVATED OLEFINS UNDER EXTREMELY MILD CONDITIONS [J].

MUKAIYAMA, T ;

WARIISHI, K ;

SAITO, Y ;

HAYASHI, M ;

KOBAYASHI, S .

CHEMISTRY LETTERS, 1988, (07) :1101-1104

[10] STEREOSELECTIVE 1,2-CIS GLYCOSYLATION REACTION OF 1-O-ACETYLRIBOSE WITH SILYLATED NUCLEOPHILES BY THE PROMOTION OF A NEW CATALYST SYSTEM [J].

MUKAIYAMA, T ;

SHIMPUKU, T ;

TAKASHIMA, T ;

KOBAYASHI, S .

CHEMISTRY LETTERS, 1989, (01) :145-148

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