Ligand-Enabled Gold-Catalyzed C(sp2)-N Cross-Coupling Reactions of Aryl Iodides with Amines

Ligand-Enabled Gold-Catalyzed C(sp2)-N Cross-Coupling Reactions of Aryl Iodides with Amines
复制标题

DOI:
10.1021/acs.orglett.9b03082
复制
发表时间:
2019-10-04
期刊:
影响因子:
5.2
通讯作者:
Patil, Nitin T.
Patil, Nitin T.
中科院分区:
化学1区
文献类型:
--
作者:
Akram, Manjur O.;Das, Avishek;Patil, Nitin T.

文献摘要

被引文献

相似文献

第一个例子的辅助(P,N)-配体使能金催化的C-N交叉偶联反应的芳基碘与胺的报告。在从头合成,后期修饰和级联过程中的反应的高度通用性,以获得官能化的吲哚啉酮和咔唑强调了所提出的策略的合成潜力。用ESI-GMS和NMR监测反应为推定的高价Au(III)中间体的原位形成提供了强有力的证据。
The first example of ancillary (P,N)-ligand-enabled gold-catalyzed C-N cross-coupling reactions of aryl iodides with amines is reported. The high generality of the reaction in de novo synthesis, late-stage modifications, and cascade processes to access functionalized indolinones and carbazoles underscores the synthetic potential of the presented strategy. Monitoring the reaction with ESI-HRMS and NMR provided strong evidence for the in situ formation of putative high valent Au(III) intermediates.