异喹啉
催化作用
部分
化学
组合化学
选择性
芳基
钯
菲
离子键合
有机化学
离子
烷基
出处
期刊:Current catalysis
[Bentham Science]
日期:2024-08-28
卷期号:13 (2)
标识
DOI:10.2174/0122115447296524240815114327
摘要
Introduction: The gold-catalyzed benzannulation reaction of oxo-alkynes with al-kenes or alkynes is one of the important and unique reactions in gold-catalyzed organic trans-formations. Methods: In this manuscript, many facets of this reaction have been discussed concerning reac-tivity and selectivity, along with a new self-benzannulation process. The scope of this chemistry was extended to construct a phenanthrene moiety. Results: In addition, a palladium-gold dual catalytic arylation of isobenzopyrylium salts using arene-diazonium salts as an aryl group source and a one-pot isoquinoline synthesis is reported for the first time. Conclusion: Moreover, a conductance measurement experiment was performed, which supports the formation of ionic species, most likely the isobenzopyrylium auric ate complex as an inter-mediate formed during the reaction process.
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