A Copper-Catalyzed Interrupted Domino Reaction for the Synthesis of Fused Triazolyl Benzothiadiazine-1-oxides

被引:3
|
作者
Hommelsheim, Rene [1 ]
Bausch, Sandra [1 ]
Selvakumar, Arjuna [1 ]
Amer, Mostafa M. [1 ,2 ]
Truong, Khai-Nghi [3 ]
Rissanen, Kari [3 ]
Bolm, Carsten [1 ]
机构
[1] Rhein Westfal TH Aachen, Inst Organ Chem, Landoltweg 1, D-52074 Aachen, Germany
[2] Egyptian Petr Res Inst, Cairo 11727, Egypt
[3] Univ Jyvaskyla, Dept Chem, POB 35, Survontie 9 B, Jyvaskyla 40014, Finland
关键词
CLICK; copper catalysis; cycloaddition; domino reactions; sulfoximines; sulfur heterocycles; ONE-POT SYNTHESIS; CLICK CHEMISTRY; ORGANIC AZIDES; HETEROCYCLIC CHEMISTRY; NITROGEN-HETEROCYCLES; ARYLATION SEQUENCE; TERMINAL ALKYNES; NATURAL-PRODUCTS; SULFOXIMINES; 1,2,3-TRIAZOLES;
D O I
10.1002/chem.202203729
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Copper(I)-catalyzed domino reactions of 2-azido sulfoximines with 1-iodoalkynes yield fused triazolyl-containing benzothiadiazine-1-oxides. The protocol features the synthesis of two fused heterocyclic rings in one step with good to excellent yields and a broad functional group tolerance. Detailed mechanistic investigations indicate that a copper pi-complex initiates a cycloaddition and oxidative C-N coupling reaction sequence. The results suggest an interrupted domino process involving an iodinated triazole as a key intermediate.
引用
收藏
页数:7
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