ASYMMETRIC ALLYLATION OF PROCHIRAL ALDEHYDES WITH A NEW ENANTIOSELECTIVE ALLYLATING AGENT PREPARED FROM STANNOUS TRIFLATE, A CHIRAL DIAMINE, AND ALLYLDIALKYLALUMINUM

被引：38

作者：

MUKAIYAMA, T

MINOWA, N

ORIYAMA, T

NARASAKA, K

机构：

来源：

CHEMISTRY LETTERS | 1986年 / 01期

关键词：

D O I：

10.1246/cl.1986.97

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：97 / 100

页数：4

共 17 条

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[3] B-ALLYLDIISOCARANYLBORANE - A NEW, REMARKABLE ENANTIOSELECTIVE ALLYLBORATING AGENT FOR PROCHIRAL ALDEHYDES - SYNTHESIS OF HOMOALLYLIC ALCOHOLS APPROACHING 100-PERCENT ENANTIOMERIC PURITIES [J].

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[6] AN ASYMMETRIC-SYNTHESIS OF GLYCEROL DERIVATIVES BY THE ENANTIOSELECTIVE ACYLATION OF PROCHIRAL GLYCEROL [J].

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CHEMISTRY LETTERS, 1984, (06) :949-952

[7] ALLYLATION OF ALDEHYDES WITH ETHERIFICATION BY DIALKOXYDICHLOROTITANIUM ALLYLTRIMETHYLSILANE - AN ASYMMETRIC VARIANT OF THE SAKURAI REACTION [J].

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[8] ENANTIOSELECTIVE CROSS ALDOL REACTION VIA DIVALENT TIN ENOLATE [J].

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[9] HIGHLY ENANTIOSELECTIVE ALDOL-TYPE REACTION OF 3-ACETYLTHIAZOLIDINE-2-THIONE WITH ACHIRAL ALDEHYDES [J].

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[10]

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