采用铜粉、硫粉、硫化钾及3-甲基吡啶在常湿、常温下直接合成了标题化合物。
The title compound has been obtained by the reaction of copper powder with sulfur powder, potassium sulfide and 3-methylpyridine at ambient temperature and normal atmosphere.
用两种方法合成了标题化合物。
合成了标题化合物，为紫色晶体，用X射线衍射法测定了晶体结构。
The title complex has been synthesized and its crystal structure has been determined by X-ray diffraction.
以菲醌为原料合成了标题化合物，通过IR和1H NM R对其结构进行了表征。
The title compound was synthesized with phenanthrenequinone as starting material and was characterized by IR and 1H NMR spectra.
采用新工艺方法，通过三步反应合成了标题化合物，并对有关的理论问题作了说明。
The title compound was synthesized with a new method in three steps. Some of the theoretical analyses concerning this compound are given.
苯甲酰硫叶立德对芳磺酰基乙烯的环加成合成了标题系列化合物，它们是一类生物活性物质。
Aryl carbonyl stabilized sulfur ylids can cycloadd to aryl vinyl sulfones to produce the title compounds. The title compounds have potentially interesting biological activity properties.
结论成功的合成了所设计的标题化合物，有助于新一代四碘苯类非离子型X线造影剂的研制。
CONCLUSION The successful synthesis of the new compound is helpful to the new generational research of tetraiodobenzene series X-ray contrast agent.
结论成功的合成了所设计的标题化合物，有助于新一代四碘苯类非离子型X线造影剂的研制。
CONCLUSION The successful synthesis of the new compound is helpful to the new generational research of tetraiodobenzene series X-ray contrast agent.
应用推荐