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.
引用
收藏
页码:3234 / 3238
页数:5
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