SYNTHESIS OF 5-FLUORO-1,3-DIOXIN-4-ONES - VERSATILE BUILDING-BLOCKS OF FLUORINATED COMPOUNDS

被引:18
作者
SATO, M
KANEKO, C
IWAOKA, T
KOBAYASHI, Y
IIDA, T
机构
[1] TOHOKU UNIV,INST PHARMACEUT,SENDAI,MIYAGI 980,JAPAN
[2] CHUGAI PHARMACEUT CO LTD,PROD TECHNOL RES LAB,KITA KU,TOKYO 115,JAPAN
[3] TOKYO COLL PHARM,HACHIOJI,TOKYO 19203,JAPAN
[4] DAIKIN IND LTD,MEC LAB,TSUKUBA,IBARAKI 305,JAPAN
关键词
D O I
10.1039/c39910000699
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Fluorination of 5,6-unsubstituted 1,3-dioxin-4-ones by fluorine followed by treatment with triethylamine affords the title compounds, which can be converted into fluorinated derivatives of either formylacetic acid or of heterocyclic systems.
引用
收藏
页码:699 / 700
页数:2
相关论文
共 10 条
[1]  
CHECH D, 1976, COLLECT CZECH CHEM C, V41, P3335
[2]   1,3-DIOXIN-4-ONES AS VERSATILE INTERMEDIATES FOR ORGANIC-SYNTHESIS [J].
KANEKO, C ;
SATO, M ;
SAKAKI, JI ;
ABE, Y .
JOURNAL OF HETEROCYCLIC CHEMISTRY, 1990, 27 (01) :25-30
[3]  
KNUNYANTS IL, 1985, SYNTHESIS FLUOROORGA
[4]   ONE-POT SYNTHESIS OF 5-FLUORO-6-ALKOXY-5,6-DIHYDROURACILS [J].
KOBAYASHI, Y ;
KUMADAKI, I ;
NAKAZATO, A .
TETRAHEDRON LETTERS, 1980, 21 (48) :4605-4606
[5]  
SATO M, 1985, SYNTHESIS-STUTTGART, P224
[6]  
SATO M, 1986, CHEM PHARM BULL, V34, P4577
[7]  
SATO M, 1986, SYNTHESIS-STUTTGART, P672
[8]  
SATO M, IN PRESS TETRAHEDRON
[9]   ADVANCES IN THE PREPARATION OF BIOLOGICALLY-ACTIVE ORGANOFLUORINE COMPOUNDS [J].
WELCH, JT .
TETRAHEDRON, 1987, 43 (14) :3123-3197
[10]  
Yoshioka H., 1990, KAGAKU TO SEIBUTSU, V28, P789