CHIRAL 3-SUBSTITUTED ALDEHYDES - DETERMINATION OF ABSOLUTE-CONFIGURATIONS AND ENANTIOMERIC EXCESSES BY NMR ANALYSIS OF DERIVED OXAZOLIDINES

被引：28

作者：

AGAMI, C ^{[1
]}

MEYNIER, F ^{[1
]}

BERLAN, J ^{[1
]}

BESACE, Y ^{[1
]}

BROCHARD, L ^{[1
]}

机构：

[1] ECOLE NATL SUPER CHIM PARIS, SYNTHESE ORGAN LAB, F-75005 PARIS, FRANCE

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1986年 / 51卷 / 01期

关键词：

D O I：

10.1021/jo00351a014

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：73 / 75

页数：3

共 31 条

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[5] DIASTEREOSELECTIVE ADDITION OF ORGANOCUPRATES TO A CHIRAL ALPHA,BETA-UNSATURATED OXAZOLIDINE - EFFECT OF A SOLVENT AND THE APPLICATION OF H-1-NMR RESULTS TO THE DETERMINATION OF THE ABSOLUTE-CONFIGURATION AND THE OPTICAL PURITY OF 3-ARYLALKANALS
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[6] REGIOSELECTIVITY OF THE REACTION OF MAGNESIUM DIALKYL CUPRATES ON ALPHA,BETA-ETHYLENIC ALDEHYDES
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[7] BRIENNE MJ, 1967, B SOC CHIM FR, P613
[8] OPTICAL ROTATORY DISPERSION STUDIES .24. EFFECT OF DISTANCE OF A SINGLE ASYMMETRIC CENTER FROM AN ALIPHATIC CARBONYL FUNCTION
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