Rh(III)-Catalyzed Chemoselective [4+2] Annulations for the Synthesis of [1,3]Oxazinoindolones: A Combined Experimental and Computational Study

被引:2
作者
Kumar, Perla Bharath [1 ,2 ]
Raju, Chittala Emmaniel [1 ,2 ]
Roy, Saikat [3 ]
Anoop, Anakuthil [3 ]
Chandra, Rajesh [1 ,2 ]
Sridhar, Balasubramanian [2 ,4 ]
Karunakar, Galla V. [1 ,2 ]
机构
[1] Indian Inst Chem Technol, Fluoro & Agrochem Div, CSIR, Hyderabad 500007, India
[2] Acad Sci & Innovat Res, Ghaziabad 201002, India
[3] Indian Inst Technol Kharagpur, Dept Chem, Kharagpur 721302, India
[4] Indian Inst Chem Technol, Ctr Xray Crystallog, CSIR, Hyderabad 500007, India
关键词
C-H BONDS; DIVERGENT SYNTHESIS; INDOLES; ALKYNES; ACCESS;
D O I
10.1021/acs.orglett.4c02770
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The interaction of N-alkoxy-1H-indole-1-carboxamides with transition metals leads to indole-fused heterocyclic scaffolds through directing group leaving/migration, [3 + 2], N-C2 [4 + 1], and [4 + 2] annulations. However, the corresponding O-C2 [4 + 2] annulation reactions have never been reported. Herein, we report the chemoselective annulation of N-alkoxy-1H-indole-1-carboxamides catalyzed by Rh(III), affording [1,3]oxazinoindolones through a hitherto unknown reaction pathway. This unprecedented C2 oxygen cyclization, rather than the known C2 nitrogen cyclization to form oxazinoindolones via five key steps, has been explained using density functional theory.
引用
收藏
页码:8680 / 8685
页数:6
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