化学
镍
催化作用
电泳剂
组合化学
化学空间
分子
纳米技术
计算化学
药物发现
有机化学
材料科学
生物化学
作者
Ramagonolla Kranthikumar
出处
期刊:Organometallics
[American Chemical Society]
日期:2022-03-04
卷期号:41 (6): 667-679
被引量:109
标识
DOI:10.1021/acs.organomet.2c00032
摘要
The formation of a new C–C bond at sp3-hybridized centers is highly desirable, as it opens up a unique, unexplored chemical space. The revolutionary discoveries in this field meet the longstanding challenge of forming stereocontrolled C–C bonds and provide rapid access to C(sp3)-rich drug molecules. The new and improved catalytic systems have enabled the creative design of challenging transformations. The latest advancements in nickel catalysis are particularly attractive and have shown excellent catalytic performance in this field. The progress that has been made toward C(sp3)–C(sp3) bond formation (traditional and cross-electrophile couplings) in the past decade is highlighted in this review.
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