化学
芳基
卡宾
亲核细胞
组合化学
反应条件
有机化学
催化作用
功能群
亲核取代
药物化学
亲核芳香族取代
亲核加成
群(周期表)
化学合成
作者
Subhashis Mukhopadhyay,Anisha Pal,Soumen Barik,Akkattu T. Biju
标识
DOI:10.1021/acs.orglett.6c02011
摘要
The N-heterocyclic carbene (NHC)-catalyzed C-H heteroarylation of aromatic aldehydes for the synthesis of aryl heteroaryl ketones under mild and metal-free conditions is reported. This operationally simple strategy proceeds via the nucleophilic substitution of aldehyde-derived Breslow intermediates with 2-chloro-substituted heteroarenes in an addition-elimination pathway following the irreversible formation of benzoin. Moreover, the reaction exhibited good functional group tolerance, providing access to a diverse range of heteroaryl ketones in moderate to high yields. In addition, the synthetic utility of the method is demonstrated through the preparation of pharmaceutically relevant molecules.
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