Conclusion 1, 2, 4-triazoles and its derivatives can be prepared by this simple method with high yield.
结论采用该方法合成1,2,4三唑及其衍生物产率高，方法简单。
Research and development of triazoles as antimicrobial agents have become one of active fields in medicinal chemistry.
三唑类抗微生物药物已成为新药研究与开发的热点领域之一。
Process for preparing 3 - substituted phenyl -5-thienyl or fully -1, 2, 4-triazoles and nove. intermediates utilized therein.
制备3-(取代的苯基)- 5 -(噻吩基或呋喃基)-1,2,4 -三唑的方法以及在其中使用的新中间体。
Treatment and prevention of neoplasms with salts of aminoimidazole carboxamide and 5-amino or substd. amino 1, 2, 3-triazoles.
用氨基咪唑甲酰胺和5 -氨基或取代的氨基1,2,3 -三唑的盐治疗和预防肿瘤。
Treatment and prevention of neoplasms with salts of aminoimidazole carboxamide and 5-amino or substituted amino 1,2,3-triazoles.
用氨基咪唑甲酰胺和5-氨基或取代的氨基1，2，3-三唑的盐治疗和预防肿瘤。
In most cases, 1, 3-dipolar cycloaddition of azides with acetylenes is the only way to synthesize substituted 1, 2, 3-triazoles.
目前，在药物合成中绝大部分的1,2,3 -三氮唑的合成方法一直沿用1,3-偶极环加成法。
The antifungal and antibacterial assay in vitro indicated that all the synthesized 1, 2, 3-triazoles exhibited different degree of inhibitory activity.
体外抗细菌、抗真菌活性表明，所合成的1,2,3 -三唑类化合物对所测细菌和真菌表现出不同程度的抑制活性。
Newly available drugs include those in the echinocandin class, including caspofungin, micafungin, and anidulafungin, as well as the newer generation triazoles, voriconazole and posaconazole.
新药物包括棘白菌素类卡泊芬净、米卡芬净和阿尼芬净，以及新一代三唑类伏立康唑和泊沙康唑。
Newly available drugs include those in the echinocandin class, including caspofungin, micafungin, and anidulafungin, as well as the newer generation triazoles, voriconazole and posaconazole.
新药物包括棘白菌素类卡泊芬净、米卡芬净和阿尼芬净，以及新一代三唑类伏立康唑和泊沙康唑。
应用推荐