化学
芳基
溴化物
催化作用
吡那考
对映选择合成
钴
锂(药物)
三氟甲基
偶联反应
组合化学
分子
功能群
有机化学
药物化学
烷基
聚合物
内分泌学
医学
作者
Weichen Huang,Xiaolong Wan,Qilong Shen
出处
期刊:Organic Letters
[American Chemical Society]
日期:2020-05-20
卷期号:22 (11): 4327-4332
被引量:38
标识
DOI:10.1021/acs.orglett.0c01363
摘要
A cobalt-catalyzed asymmetric cross-coupling of α-bromo-α-fluorotoluene derivatives with a variety of aryl zincates derived from lithium aryl n-butyl pinacol boronates and ZnBr2 under mild reaction conditions was described. In addition to mild reaction conditions, another advantage includes the compatibility of various common functional groups such as fluoride, chloride, bromide, cyano, or ester groups. Furthermore, this protocol was successfully applied to the enantioselective synthesis of three fluorinated derivatives of biologically active compounds or drug molecules.
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