胺化
钯
氢胺化
催化作用
化学
组合化学
分子间力
多米诺骨牌
有机化学
分子
作者
Michael S. Christodoulou,Egle M. Beccalli,Sabrina Giofrè
出处
期刊:Catalysts
[MDPI AG]
日期:2020-06-06
卷期号:10 (6): 634-634
被引量:14
标识
DOI:10.3390/catal10060634
摘要
This review is focused on palladium-catalyzed reactions as efficient strategies aimed at the synthesis of different classes of benzodiazepines. Several reaction typologies are reported including hydroamination, amination, C–H arylation, N-arylation, and the Buchwald–Hartwig reaction, depending on the different substrates identified as halogenated starting materials (activated substrates) or unactivated unsaturated systems, which then exploit Pd(0)- or Pd(II)-catalytic species. In particular, the use of the domino reactions, as intra- or intermolecular processes, are reported as an efficient and eco-compatible tool to obtain differently functionalized benzodiazepines. Different domino reaction typologies are the carboamination, aminoarylation, aminoacethoxylation, aminohalogenation, and aminoazidation.
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