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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.
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页码:7822 / 7827
页数:6
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