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Three-component synthesis of 1,4-benzothiazines via iodide-catalyzed aerobic C-H sulfuration with elemental sulfur
被引:17
|作者:
Jiang, Jingjing
[1
]
Tuo, Xiaotong
[1
]
Fu, Zhuquan
[1
]
Huang, Huawen
[1
]
Deng, Guo-Jun
[1
]
机构:
[1] Xiangtan Univ, Coll Chem, Key Lab Green Organ Synth & Applicat Hunan Prov, Key Lab Environm Friendly Chem & Applicat,Minist, Xiangtan 411105, Peoples R China
基金:
中国国家自然科学基金;
关键词:
CONTROLLED SELECTIVE SYNTHESIS;
TRISULFUR RADICAL-ANION;
S BOND FORMATION;
MOLECULAR-OXYGEN;
FACILE SYNTHESIS;
DERIVATIVES;
THIAZOLES;
FUNCTIONALIZATION;
OXIDATION;
INDOLES;
D O I:
10.1039/d0ob00074d
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
Herein, iodide-catalyzed aerobic synthesis of 1,4-benzothiazines via functionalization of multiple C-H bonds with elemental sulfur is described. Beyond the well-established thiazole formation from elemental sulfur, this method provides the first access to the corresponding six-membered N,S-heterocyclic products via direct functionalization of multiple C-H bonds. Hence, 1,4-benzothiazine products were generated in satisfactory yields with a range of compatible functionalities.
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页码:3234 / 3238
页数:5
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