Directing group assisted para-selective C-H alkynylation of unbiased arenes enabled by rhodium catalysis

被引:2
作者
Dutta, Uttam [1 ]
Prakash, Gaurav [1 ]
Devi, Kirti [1 ]
Borah, Kongkona [1 ]
Zhang, Xinglong [2 ]
Maiti, Debabrata [1 ]
机构
[1] Indian Inst Technol, Dept Chem, Mumbai 400076, Maharashtra, India
[2] ASTAR, Inst High Performance Comp IHPC, Singapore, Singapore
关键词
ORTHO-ETHYNYLATION; BASIS-SETS; BONDS; GOLD; DIFLUOROMETHYLATION; BORYLATION; ALKYLATION; AMIDES; META; FUNCTIONALIZATION;
D O I
10.1039/d3sc03528j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Regioselective C-H alkynylation of arenes via C-H activation is challenging yet a highly desirable transformation. In this regard, directing group assisted C(sp2)-H alkynylation of arenes offers a unique opportunity to ensure precise regioselectivity. While the existing methods are mainly centered around ortho-C-H alkynylation and a few for meta-C-H alkynylation, the DG-assisted para-selective C-H alkynylation is yet to be reported. Herein we disclose the first report on Rh-catalyzed para-C-H alkynylation of sterically and electronically unbiased arenes. The para-selectivity is achieved with the assistance of a cyano-based directing template and the selectivity remained unaltered irrespective of the steric and electronic influence of the substituents. The post-synthetic modification of synthesized para-alkynylated arenes is also demonstrated. The mechanistic intricacies of the developed protocol are elucidated through experimental and computational studies. A first work on rhodium-catalyzed para-selective C-H alkynylation has been reported and its mechanistic insights were gleaned from experimental and computational studies.
引用
收藏
页码:11381 / 11388
页数:8
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