1,4-CHIRALITY TRANSFER VIA THE ESTER ENOLATE CLAISEN REARRANGEMENT

被引：18

作者：

NAGATSUMA, M ^{[1
]}

SHIRAI, F ^{[1
]}

SAYO, N ^{[1
]}

NAKAI, T ^{[1
]}

机构：

[1] TOKYO INST TECHNOL, DEPT CHEM TECHNOL, MEGURO KU, TOKYO 152, JAPAN

来源：

CHEMISTRY LETTERS | 1984年 / 08期

关键词：

D O I：

10.1246/cl.1984.1393

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：1393 / 1396

页数：4

共 12 条

[1]

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[7] STEREOCHEMICAL CONTROL THROUGH SIGMATROPIC REARRANGEMENTS - THEIR MECHANISTIC GROUNDS AND SYNTHETIC POTENTIALS AS METHODOLOGIES FOR ACYCLIC STEREOCONTROL [J].

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[8] 1,4-CHIRALITY TRANSFER VIA THE [2,3]-WITTIG REARRANGEMENT OF CHIRAL ALLYLIC PROPARGYL ETHER SYSTEM - A NEW, PRACTICAL ENTRY TO CHIRAL PROPARGYLIC ALCOHOLS [J].

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CHEMISTRY LETTERS, 1984, (02) :255-258

[9] ACYCLIC STEREOCONTROL VIA ASYMMETRIC [2,3]-WITTIG REARRANGEMENT WITH HIGH ENANTIO-SELECTIVITY AND ERYTHRO-SELECTIVITY AND ITS USE IN THE CHIRAL SYNTHESIS OF INSECT PHEROMONES [J].

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[10] HIGHLY ENANTIOSPECIFIC AND ERYTHRO-SELECTIVE [2,3]-WITTIG REARRANGEMENT OF ENANTIOMERICALLY-ENRICHED ALLYLIC BENZYL ETHERS - A NEW, FORMAL CHIRAL SYNTHESIS OF 1-EPHEDRINE [J].

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CHEMISTRY LETTERS, 1984, (02) :259-262

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