SYNTHESIS AND C-13 FT NMR-SPECTROSCOPY OF FURAN-2,3-DIONE DERIVATIVES

被引：0
|
作者：
HNACH, M
AYCARD, JP
ZINEDDINE, H
机构：
[1] UNIV AIX MARSEILLE 1,CTR ST JEROME,PHYS INTERACT ION & MOLEC LAB,CNRS,URA 773,CASE 542,F-13397 MARSEILLE 4,FRANCE
[2] UNIV MOULAY ISMAIL,FAC SCI,DEPT CHIM,MEKNES,MOROCCO
来源：
BULLETIN DE LA SOCIETE CHIMIQUE DE FRANCE | 1991年 / 03期
关键词：
FURAN-2,3-DIONE; H-1 AND C-13 NMR; UV AND IR SPECTRA;
D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
Substituted furan-2,3-diones were obtained by condensation of oxalyl chloride with silyl enol ether of para-substituted acetophenones (R = H, CH3, OCH3, Cl, Br, F), propiophenone, 1-tetralone, 6-methoxytetralone and 1-benzosuberone. The spectroscopic data obtained from IR, UV, H-1 and C-13 NMR studies are quite similar whichever are the substituents.
引用
收藏
页码：393 / 396
页数：4
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