321724-11-2Relevant academic research and scientific papers
Synthesis of 6,7-Dihydro-5H-imidazo[1,2-a]imidazole-3-sulfonic acid amides
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Page/Page column 10; 20, (2010/11/28)
Disclosed is an improved multi-step process for preparing a compound of Formula I: wherein R1 to R3 are as defined herein. The compounds of formula I inhibit the binding of human intercellular adhesion molecules to the Leukointegrins
A practical synthesis of LFA-1 inhibitors utilizing CuCl-promoted intramolecular cyclization of thiohydantoins
Wang, Xiao-Jun,Zhang, Li,Xu, Yibo,Krishnamurthy, Dhileepkumar,Varsolona, Richard,Nummy, Laurence,Shen, Sherry,Frutos, Rogelio P.,Byrne, Denis,Chung,Farina, Vittorio,Senanayake, Chris H.
, p. 273 - 276 (2007/10/03)
An efficient and chromatography-free approach for synthesis of a new class of LFA-1 inhibitors was developed. A copper(I) chloride-promoted intramolecular cyclization of thiohydantoins 7a-b serves as a key step to highly functionalized bicyclic guanidines
