DIASTEREOISOMERIC MUTATOCHROMES - SEPARATION, ABSOLUTE-CONFIGURATION, AND SPECTRA AND CHROMATOGRAPHIC BEHAVIOR

被引：14

作者：

ESCHENMOSER, W ^{[1
]}

MARKIFISCHER, E ^{[1
]}

EUGSTER, CH ^{[1
]}

机构：

[1] UNIV ZURICH,INST ORGAN CHEM,CH-8057 ZURICH,SWITZERLAND

来源：

HELVETICA CHIMICA ACTA | 1984年 / 67卷 / 01期

关键词：

D O I：

10.1002/hlca.19840670121

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：170 / 174

页数：5

共 27 条

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[8] SYNTHESIS AND CHIRALITY OF (5R,6R)-5,6-DIHYDRO-BETA,PSI-CAROTENE-5,6-DIOL, (5R,6R,6'R)-5,6-DIHYDRO-BETA,EPSILON-CAROTENE-5,6-DIOL, (5S,6R)-5,6-EPOXY-5,6-DIHYDRO-BETA,PSI-CAROTENE AND (5S,6R6'R)-5,6-EPOXY-5,6-DIHYDRO-BETA,EPSILON-CAROTENE [J].

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[9] SYNTHESIS OF (+)-(5S,6S)-AZAFRIN METHYL-ESTER - ABSOLUTE-CONFIGURATION OF AEGINETIC ACID AND OF FURTHER VICINAL APOCAROTENE-DIOLS [J].

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[10] SYNTHESIS AND CHIRALITY OF (5S,6R)-5,6-EPOXY-5,6-DIHYDRO-BETA,BETA-CAROTENE AND (5R,6R)-5,6-DIHYDRO-BETA,BETA-CAROTENE-5,6-DIOL, A COMPOUND WITH UNEXPECTED SOLUBILITY CHARACTERISTICS [J].

ESCHENMOSER, W ;

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HELVETICA CHIMICA ACTA, 1978, 61 (02) :822-831

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