Oxindole

Study on green process for synthesis of oxindole

氧化吲哚的绿色合成工艺研究

It was further converted to oxindole through reduction by hydrazine hydrate in water , catalyzed by ( FeO ( OH )) .

在水溶液中，以FeO（OH）为催化剂，水合肼还原邻硝基苯乙酸得到氧化吲哚。

Method Eight compounds were synthesized by condensation between oxindole and benzaldehyde derivatives under microwave irradiation , and their antitumor activities were assayed using human HepG_2 cells .

方法以吲哚酮和苯甲醛衍生物在微波辐射条件下进行缩合反应制得目标化合物，用人肝癌HepG2细胞进行抗肿瘤活性检测。

OBJECTIVE : A facile synthesis of sodium salt of 5 chloro 3 ( 2 thenoyl ) 2 oxindole 1 carboxyamide from common 4 chloroaniline is described .

目的：合成具抗炎活性的5氯3（2噻吩甲酰）1甲酰胺2羟基吲哚钠盐。

The substituted indole , 3 methylindole , was hydroxylated at the 2 position but not at the 3 position and could not be further metabolized through the oxindole isatin pathway .

3甲基吲哚可在2位上羰基化，但不能在3位上羰基化，所以不能通过氧化吲哚&靛红途径进行代谢。