Electronic substituent effects of furoxan and furazan systems

被引:6
作者
Fruttero, R
Boschi, D
Fornatto, E
Serafino, A
Gasco, A
Exner, O
机构
[1] Fac Farm, Dept Sci & Tecnol Farm, I-10125 Turin, Italy
[2] Acad Sci Czech Republ, Inst Organ Chem & Biochem, CR-16610 Prague 6, Czech Republic
来源
JOURNAL OF CHEMICAL RESEARCH-S | 1998年 / 09期
关键词
D O I
10.1039/a803585g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Heterocyclic systems 3-furoxanyl, 4-furoxanyl and 3-furazanyl have been characterised as substituents by their substituent constants sigma(m), sigma(p), sigma(1) and sigma(R), determined from pK and F-19 NMR shifts: they are strongly electron attracting but weakly conjugated.
引用
收藏
页码:495 / 495A
页数:3
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