An article Regioselective C-H Thioarylation of Electron-Rich Arenes by Iron(III) Triflimide Catalysis WOS:000641292800044 published article about BOND FUNCTIONALIZATIONS; ARYL CHALCOGENIDES; BORONIC ACIDS; THIOLS; SULFIDES; DICHALCOGENIDES; SULFENYLATION; DERIVATIVES; THIOETHERS in [Dodds, Amy C.; Sutherland, Andrew] Univ Glasgow, Sch Chem, WestCHEM, Joseph Black Bldg, Glasgow G12 8QQ, Lanark, Scotland in 2021, Cited 59. The Name is 1,3-Dimethoxybenzene. Through research, I have a further understanding and discovery of 151-10-0. Name: 1,3-Dimethoxybenzene
A mild and regioselective method for the preparation of unsymmetrical biaryl sulfides using iron(III) catalysis is described. Activation of N-(arylthio)succinimides using the powerful Lewis acid iron(III) triflimide allowed the efficient thiolation of a range of arenes, including anisoles, phenols, acetanilides, and N-heterocycles. The method was applicable for the late-stage thiolation of tyrosine and tryptophan derivatives and was used as the key step for the synthesis of pharmaceutically relevant biaryl sulfur-containing compounds such as the antibiotic dapsone and the antidepressant vortioxetine. Kinetic studies revealed that while N-(arylthio)succinimides lbearing electron-deficient arenes underwent thioarylation catalyzed entirely by iron(III) triflimide, N-(arylthio)succinimides with electron-rich arenes displayed an autocatalytic mechanism promoted by the Lewis basic product.
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Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com