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1)  4-oxo-thiazolidine
4-羰基噻唑烷酮
2)  4-thiazolidone
4-噻唑烷酮
1.
3-Substituted-2-acylimino-4-thiazolidones were synthesized by reaction of N-substituted-N'-benzoyl (or acetyl) ureas with haloacetic acid or ethyl α-bromoacetate and its 5-acetic acid compounds were obtained by reaction of N-aryl-N'-benzoyl ureas with maleic anhydride.
通过N-烃基-N′-酰基硫脲和卤代乙酸(或卤代乙酸酯)反应,合成了一些新的3-取代-2-酰亚胺-4-噻唑烷酮类化合物,并对反应机理作了探讨。
3)  thiazolidin-4-one
噻唑烷-4-酮
1.
Microwave Assisted Synthesis and Antibacterial Study of 3-Naphthyl-2-[(un)substituted phenyl]-1,3-thiazolidin-4-ones;
新型3-萘基-1,3-噻唑烷-4-酮衍生物的微波促进合成及其抗菌活性研究
2.
Microwave Assisted Synthesis and Antifungal, Anti-tumor Study of 2-(2,6-Dichlorophenyl)-1,3-thiazolidin-4-ones
2-(2,6-二氯苯基)-1,3-噻唑烷-4-酮衍生物的微波促进合成及抗真菌、抗肿瘤活性研究
4)  thiazolidonyl
噻唑烷酮基
5)  N-Carboalkoxy(aryloxy)-2-thiazolidinones
N-烃氧羰基-2-噻唑烷酮衍生物
1.
Synthesis and Fungicidal Activities of N-Carboalkoxy(aryloxy)-2-thiazolidinones;
N-烃氧羰基-2-噻唑烷酮衍生物的合成及其杀菌活性(英文)
6)  5-(4-hydroxybenzyl)thiazolidine-2-4-dione
5-(4-羟基苄基)噻唑烷-2,4-二酮
补充资料:1,4-二乙氧羰基-3-吡咯烷酮
分子式:C10H15NO5
分子量:229.23
CAS号:142288-14-0

性质:暂无

制备方法:用甘氨酸与丙烯腈加成,生成N-氰乙基甘氨酸,然后水解并与乙醇在酸催化下酯化得N-乙氧羰基乙基甘氨酸乙酯,进而在乙醇钠作用下环合制得该品。

用途:南瓜子氨酸氢溴酸盐的中间体。

说明:补充资料仅用于学习参考,请勿用于其它任何用途。
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