杀菌剂
范围(计算机科学)
计算机科学
协议(科学)
翻译(生物学)
钥匙(锁)
简单(哲学)
组合化学
化学
程序设计语言
生物
植物
医学
操作系统
生物化学
哲学
基因
信使核糖核酸
认识论
病理
替代医学
作者
Yue Zhang,Zhen Chen,Jing Nie,Fa‐Guang Zhang,Jun‐An Ma
标识
DOI:10.1021/acs.joc.9b00819
摘要
Herein, we present a facile approach to a diverse collection of 1,4-disubstituted 3-di- or mono-fluoromethylpyrazoles utilizing our previously developed cyanopyrazoles as key building blocks. This method features several merits, such as easily accessible starting materials, broad substrate scope, mild reaction conditions, and simple operation. This protocol further deserves to be highlighted by the successful translation into the synthesis of commercialized fungicide fluxapyroxad and its analogues.
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