化学
亲核细胞
试剂
有机合成
脱羧
组合化学
亲核加成
有机化学
多样性(控制论)
催化作用
计算机科学
人工智能
作者
Serhii Melnykov,V. A. Sukach,М. В. Вовк
标识
DOI:10.2174/1385272824999200818181531
摘要
Decarboxylative addition reactions are well known as an effective approach to C–C bonds formation due to the availability of starting reagents, ease of handling, and low environmental impact. This approach clearly demonstrated its potential for the synthesis of the variety of acyclic and heterocyclic compounds, including optically active ones. The significant amount of articles devoted to this topic published in recent years proves the importance of this approach in modern organic synthesis. In this review, the recent achievements in decarboxylative addition to C=C, C=N, and C=O bonds have been summarized and discussed over the last 6 years.
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