76148-56-6Relevant articles and documents
AIBN-Promoted Synthesis of Bibenzo[ b][1,4]thiazines by the Condensation of 2,2′-Dithiodianiline with Methyl Aryl Ketones
Huang, Xianqiang,Rong, Nianxin,Li, Pengfei,Shen, Guodong,Li, Qiang,Xin, Nana,Cui, Chuansheng,Cui, Jichui,Yang, Bingchuan,Li, Dacheng,Zhao, Changqiu,Dou, Jianmin,Wang, Bo
supporting information, p. 3332 - 3336 (2018/06/11)
A series of bibenzo[b][1,4]thiazines with various functional groups has been synthesized by a free-radical condensation reaction. Bibenzo[b][1,4]thiazines were obtained in moderate to good yield (up to 85%) through a one-step reaction of readily available 2,2′-dithiodianiline and methyl aryl ketones with AIBN as radical initiator in HOAc. Bibenzo[b][1,4]thiazines exhibit diversiform solid-state packing.
New dyes based on 3-aryl-benzo- and -naphtho-1,4-thiazines
MacKenzie, Neil E.,Thomson, Ronald H.,Greenhalgh, Colin W.
, p. 2923 - 2932 (2007/10/02)
3-Aryl-2H-1,4-benzothiazines have been converted into cyanine dyes by condensing their hydroperchlorates with aldehydes, and into azo-compounds by coupling with reactive diazonium salts. The azo-compounds were also obtained by condensing arylglyoxal hydra