Nitration of sydnones. Reaction with 3-arylsydnones containing electron-donors on the aryl ring

被引:8
作者
Turnbull, K
Blackburn, TL
Miller, JJ
机构
[1] Department of Chemistry, Wright State University, Dayton
关键词
D O I
10.1002/jhet.5570330244
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Exclusive aryl ring nitration of a series of 3-arylsydnones 1 with electron donors (di- or tri-methyl) on the aryl ring is reported.
引用
收藏
页码:485 / 487
页数:3
相关论文
共 6 条
[1]   BROMINATION OF SYDNONES .2. BROMINATION OF 3-(2-AMINOPHENYL)SYDNONE AND RELATED-COMPOUNDS [J].
HODSON, SJ ;
TURNBULL, K .
JOURNAL OF HETEROCYCLIC CHEMISTRY, 1985, 22 (05) :1223-1227
[2]  
OHTA M, 1969, NONBENZENOID AROMATI, V1, P146
[3]   SN MECHANISM IN AROMATIC COMPOUNDS .PART 30. SYDNONE RING [J].
TINLOK, C ;
MILLER, J ;
STANSFIELD, F .
JOURNAL OF THE CHEMICAL SOCIETY, 1964, (APR) :1213-&
[5]   C-13 NMR-STUDIES ON 3-ARYL-4-CYANOSYDNONES (II) - NMR-SPECTROSCOPY AND THE CHAIN-CONJUGATED STRUCTURE OF SYDNONES [J].
WANG, SP ;
KUO, CN ;
MA, S ;
YEH, MY .
SPECTROSCOPY LETTERS, 1993, 26 (03) :431-445
[6]  
WEINTRAUB PM, 1969, TETRAHEDRON LETT, P579