Dual Copper Photoredox C-H Alkynylation with Arylacetylenes

被引:4
作者
Nair, Akshay M. [1 ]
Rahaman, Rajjakfur [1 ]
Patra, Jatin [1 ]
Volla, Chandra M. R. [1 ]
机构
[1] Indian Inst Technol, Dept Chem, Mumbai 400076, India
关键词
REGIOSELECTIVE SYNTHESIS; TERMINAL ALKYNES; ANNULATION; CATALYSIS; ARENES; BONDS;
D O I
10.1021/acs.orglett.4c02578
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
In the realm of organic synthesis, direct C-H alkynylation with arylacetylenes has remained a daunting challenge due to competing annulations or alkenylation. Addressing this long-standing issue, herein we demonstrate the merging of copper and photocatalysis to achieve the elusive C-H alkynylation of benzamides using arylacetylenes or arylpropiolic acids. Unlike conventional copper-mediated C-H activations, our protocol circumvents the need for high temperatures and stoichiometric amounts of copper salts or metal/non-metal oxidants. The versatility of the developed dual copper photoredox system is underscored by performing other diverse C-H functionalizations such as amination, selenylation, arylation, sulfonylation, and nitration under slightly modified conditions.
引用
收藏
页码:7822 / 7827
页数:6
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