835917-10-7Relevant academic research and scientific papers
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
A practical synthesis of highly functionalized fused 1,6-dihydroimidazo-[1, 2-a]imidazole-2,5-diones, key intermediates for LFA-1 inhibitors
Wang, Xiao-Jun,Xu, Yibo,Zhang, Li,Krishnamurthy, Dhileepkumar,Nummy, Laurence,Farina, Vittorio,Senanayake, Chris H.
, p. 2800 - 2802 (2007/10/03)
An alternative and chromatography-free approach for synthesis of a new class of LFA-1 inhibitors was developed. A key feature of this process involved a transformation of thioureas 14 to acyclic guanidine derivatives 9 followed by intramolecular cyclizati
