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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.
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页数:7
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