An article Three-component synthesis of 1,4-benzothiazines via iodide-catalyzed aerobic C-H sulfuration with elemental sulfur WOS:000532260100003 published article about CONTROLLED SELECTIVE SYNTHESIS; TRISULFUR RADICAL-ANION; S BOND FORMATION; MOLECULAR-OXYGEN; FACILE SYNTHESIS; DERIVATIVES; THIAZOLES; FUNCTIONALIZATION; OXIDATION; INDOLES in [Jiang, Jingjing; Tuo, Xiaotong; Fu, Zhuquan; Huang, Huawen; Deng, Guo-Jun] Xiangtan Univ, Coll Chem, Key Lab Green Organ Synth & Applicat Hunan Prov, Key Lab Environm Friendly Chem & Applicat,Minist, Xiangtan 411105, Peoples R China in 2020, Cited 77. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6. Product Details of 100-19-6
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.
Product Details of 100-19-6. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Jiang, JJ; Tuo, XT; Fu, ZQ; Huang, HW; Deng, GJ or concate me.
Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem