1) furoxan derivatives
氧化呋咱衍生物
1.
Dimerization reaction of cyanide oxide leads to formation the furoxan derivatives with symmetrical substituent groups.
总结了氧化氰结构的制备方法及其优缺点,如羟肟酰氯与弱碱的作用、醛肟与氧化氮作用、肼钾盐与氧化剂作用等,以及由氧化氰二聚反应获得的具有不同对称结构的氧化呋咱衍生物。
2) Furoxan-coupled diclofenac compounds
呋咱氮氧化物偶联的双氯芬酸衍生物
3) furoxan
呋咱氮氧化物
1.
Study on NO-Donating Antihypertensive AgentsⅠ. Synthesis and Antihypertensive Activity of C-3 Nitrate or Furoxan Substituted Benzopyrans;
一氧化氮供体型抗高血压药物的研究Ⅰ.C-3位具有硝酸酯和呋咱氮氧化物取代结构的苯骈吡喃类化合物的合成及其降压活性
2.
Studies on Synthesis and NO-release in Vitro Activity of the New Drugs Containing Furoxanyl Moiety;
新呋咱氮氧化物类NO供体药物合成及体外NO释放测试
3.
The protected p-coumaric acid was esterified with corresponding hydroxyfuroxan, and the re-sulted ester was deprotected and condensed with aspirin to give II1～II3, respectively.
对羟基桂皮酸酚羟基经保护后与相应的羟基呋咱氮氧化物酯化,酯化物脱保护,再与阿司匹林缩合得II1～II3;对羟基桂皮酸与相应二溴烷烃作用,再经阿司匹林酯化,得到的溴代烷基酯与硝酸银反应得II4～II7;酚羟基保护的对羟基桂皮酸与异山梨醇单硝酸酯酯化,脱保护后与阿司匹林缩合得II8。
4) furoxans
呋咱氮类氧化物
5) furoxan
氧化呋咱
1.
Synthesis and Properties of Pentanitrohexaazatricyclotetradecanedifuroxan;
五硝基六氮杂三环十四烷并双氧化呋咱的合成和性质
2.
Synthesis of Hexanitrohexaazatricyclotetradecanedifuroxan;
六硝基六氮杂三环十四烷并双氧化呋咱的合成
3.
Theoretical Calculation of the Detonation Parameters of New Furazan(furoxan) Explosives;
新型呋咱(氧化呋咱)类炸药爆轰参数的理论计算
6) furazan (furoxan)
呋咱(氧化呋咱)
补充资料：氯磺酸及其衍生物
氯磺酸及其衍生物
Chlorosulfonic Acid and Its Derivatives
lohuangsuan jiqi yanshengwu氯磺酸及其衍生物Chlorosulfonie Aeid and Its Derivative号赵季芝太原化工厂汪金铝太原化工厂1.2.2 .1.2 .2.3.3 .1.3 .2.3 .3.4.4 .1.4 .2.4 .2.1.概述······························”··········……217性质·…，·····································……217物理性质····································……217化学牲质····································……217生产方法····································……218气相合成法·································……218气一液相合成法···························……219技术进展····································……219经济概况····································……219国内外生产现状···························……219技术经济状况············……;..·········……22。消耗定额························“··········……2204 .2.2.5.5 .1.5 .2.6。7。
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