Iron-Catalyzed S-Arylation of Benzothiazole with Aryl Iodides under Aqueous Medium: Facile Synthesis of Aryl(2-aminoaryl) Sulfides

Autor:	Hang Wai Lee, Ka Fu Yung, Fuk Yee Kwong
Rok vydání:	2014
Předmět:	chemistry.chemical_classification Aqueous medium Sulfide Ligand Chemistry Aryl Organic Chemistry Chloride Combinatorial chemistry Catalysis chemistry.chemical_compound Benzothiazole Diamine medicine medicine.drug
Zdroj:	Synlett. 25:2743-2747
ISSN:	1437-2096 0936-5214
DOI:	10.1055/s-0034-1379484
Popis:	A simple route for facile access of aryl(2-aminoaryl) sulfide was reported. With the aid of iron(III) chloride catalyst and diamine ligand, benzothiazole was efficiently S-arylated with various aryl iodides (19 examples) in water under air atmosphere. This operationally simple protocol provides aryl(2-aminoaryl) sulfides in moderate to good yields.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::c480cc9aace2b7fb659fda4dc5e5ca9f https://doi.org/10.1055/s-0034-1379484 Zobrazit plný text záznamu