53691-65-9Relevant academic research and scientific papers
Transition-Metal-Free Synthesis of N-Arylphenothiazines through an N- And S-Arylation Sequence
Matsuzawa, Tsubasa,Hosoya, Takamitsu,Yoshida, Suguru
supporting information, p. 2347 - 2352 (2021/04/05)
An efficient synthetic method of N-arylphenothiazines from o-sulfanylanilines under transition-metal-free conditions is disclosed. An N- and S-arylation sequence of o-sulfanylanilines enabled us to synthesize a wide variety of N-arylphenothiazines. In par
Heterogeneous copper-catalyzed synthesis of S-arylated 2-aminothiophenols via ring opening of benzothiazoles and C-S coupling using aryl halides
Ichikawa, Tomohiro,Matsuo, Tomohiro,Tachikawa, Takumu,Sawama, Yoshinari,Monguchi, Yasunari,Sajiki, Hironao
, p. 793 - 805 (2019/04/26)
Chelate resins, which are polystyrene-divinylbenezene-based polymers bearing iminodiacetic acids or polyamines as ligands, supported copper catalysts (Cu/CR11 or Cu/CR20) in effectively catalyzing the ring cleaving S-arylation of benzothiazole with aryl i
Iron-catalyzed S-arylation of benzothiazole with aryl iodides under aqueous medium: Facile synthesis of aryl(2-aminoaryl) sulfides
Lee, Hang Wai,Yung, Ka Fu,Kwong, Fuk Yee
supporting information, p. 2743 - 2747 (2015/01/08)
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.
Iron-Catalyzed S-Arylation of Benzothiazole with Aryl Iodides under Aqueous Medium: Facile Synthesis of Aryl(2-aminoaryl) Sulfides
Lee, Hang Wai,Yung, Ka Fu,Kwong, Fuk Yee
, p. 2743 - 2747 (2015/05/05)
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.
