基本释义:

溴代樟脑

网络释义

1)bromcamphor,溴代樟脑

2)D-3-bromophor-8-sulfonic acid ammonium salt,D-3-溴代樟脑-8-磺酸铵

3)bromination,溴代

4)bromization,溴代

5)aryl bromide,溴代芳烃

6)α-bromoketone,α-溴代酮

用法和例句

Study on synthesis bromination derivatives of polyethylene glycol monomethyl ether;

聚乙二醇单甲醚溴代衍生物的合成研究

Comparing to different reaction methods, the method starting from 1,3-dimethyladamantane was certified with the memantine hydrochloride synthesized by bromination ,acetimidolation, hydrolysis and acidation.

通过比较不同的反应路线,确定了以1,3-二甲基金刚烷为原料,经溴代、乙酰氨基化、水解反应最后经酸化得到盐酸美金刚胺。

Bromacil was synthesized using 2-bromobutane and urea as the starting materials in three steps including condensation,cyclization and bromination with total yield of 61%.

以2-溴丁烷和尿素作为起始原料,经缩合、环化、溴代三步反应得到除草定,总收率为61%。

The Study on Bromization of Benzene on the Platinum Electrode By Confocal Microprobe Raman Spectroscopy;

苯在铂电极上溴代反应的共焦显微拉曼光谱研究

Suzuki cross-coupling reactions between aryl bromides and phenylboronic acids were studied over a hydroxyapatite-supported Mn catalyst(MnHAP) for the first time.

对于不同取代基取代的溴代芳烃或苯硼酸,可以得到中等产率(18%~46%)的偶联产物。

The palladium catalyst supported on fluoride pillared layered double hydroxide(LDH-F) was prepared by the incipient wetness method,and it was used to catalyze the Heck and Suzuki coupling reactions of aryl bromides.

以氟离子插层的水滑石LDH-F为载体,用逐滴浸渍法制备了新型Pd/LDH-F催化剂,并用其催化溴代芳烃的Heck和Suzuki偶联反应。

6 were obtained from thioamides and α-bromoketones by a four-step reaction.

以硫代酰胺和α-溴代酮为原料,经4步反应合成了N,N′-二酰基肼(6),6在POCl3作用下脱水环化,合成了7个未见文献报道的2-芳基-5-[(4-芳基噻唑-2-基)甲基]-1,3,4-噁二唑类化合物,其结构经1H NMR,IR,MS和元素分析表征。

Quinoxalines were obtained from α-bromoketones,1,2-diaminobenzene and DMSO in a solvent-free one-pot process at room temperature under grinding.

在室温无溶剂条件下,将α-溴代酮、邻苯二胺和二甲亚砜(DMSO)置于研钵中研磨,一锅法合成了一系列喹喔啉类化合物。

On the basis of this, the additionreactions of N-sulfonylimines with α-bromoketones and α-bromoesters in the presentof zinc powder were carried out.

在此基础上又研究了α-溴代酮和α-溴代酯在金属锌的作用下与磺酰亚胺的加成反应。