25752-18-5Relevant academic research and scientific papers
Approach for 2-(arylthio)imidazoles and imidazo[2,1-b]thiazoles from imidazo[2,1-b][1,3,4]thiadiazoles by ring-opening and -reconstruction
Shi, Benyi,Zhu, Zhouhe,Zhu, Yi-Shuo,Zhou, Dagang,Wang, Jinyuan,Zhou, Panpan,Jing, Huanwang
supporting information, p. 2978 - 2984 (2016/03/12)
A highly efficient one-pot synthesis of imidazo[2,1-b]thiazole derivatives has been developed and proceeds via a ring-opening and ring-closing reconstruction of imidazo[2,1-b][1,3,4]thiadiazoles with phenylacetylene in the presence of potassium tert-butox
Reinvestigation of 1,3,4-thiadiazol-2(3h)-iminium bromide in the two-step synthesis of imidazo[2,1-b][1,3,4]- thiadiazoles
Sano, Shigeki,Matsuura, Keisuke,Sumiyoshi, Hayato,Miki, Akira,Kitaike, Syuji,Nakao, Michiyasu
, p. 1041 - 1053 (2014/04/17)
The synthesis of 1,3,4-thiadiazol-2(3H)-iminium bromides, which are intermediates in the most commonly used synthetic approach to imidazo[2,1-b][1,3,4]thiadiazoles, and a single crystal X-ray diffraction study of one of these iminium bromides are describe
Synthesis of imidazo[2,1-b[-1,3,4-thiadiazoles in DABCO as an efficient and recyclable catalyst
Tiwari, Kamleshwar,Verma, Pankaj Kumar,Singh, Shyam Babu,Singh, Jagdamba
scheme or table, p. 3021 - 3030 (2012/07/28)
An efficient and general method has been described for the synthesis of imidazo[2,1-b]-1,3,4-thiadiazole by the reaction of 2-aminothiadiazoles with phenacyl bromides in the presence of 1,4-diazabicyclo[2.2.2]octane (DABCO). The method is suitable for the synthesis of functionalized imidazothiadiazoles.
Green synthesis of substituted imidazothiadiazoles using ionic liquid
Kidwai, Mazaahir,Rastogi, Shweta
, p. 2321 - 2324 (2007/10/03)
An eco-friendly facile synthesis of imidazo[2,1-b]-1,3,4-thiadiazoles is described using ionic liquid, [bmim]PF6 (1-butyl-3-methylimidazolium hexafluorophosphate). The use of recyclable catalyst demonstrates the advantages of significant rate e
Acid azo dyes containing heterocyclic couplers
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, (2008/06/13)
Disclosed are novel acid azo dyes containing a sulfonated, sulfated or thiosulfated organothiothiadiazole azo moiety and a heterocyclic coupler which may be substituted. The dyes produce reddish-yellow to orange shades on, for example, hydrophobic textile
Indoline coupled isothiazole azo dyes
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, (2008/06/13)
Disclosed are novel azo dyes containing an isothiazole azo moiety which may be substituted, and a heterocyclic coupler which also may be substituted. The dyes produce yellow shades on, for example, hydrophobic textile fiber including polyesters, polyamide
