188262-96-6Relevant academic research and scientific papers
Silver(I)-Catalyzed Tandem Sigamatropic Rearrangement/1,3-H Shift/6π Aza-electrocyclization of N-Propargylic Hydrazones: A Mild Synthetic Route to 1,6-Dihydropyridazines
Ding, Zong-Cang,Ju, Lu-Chuan,Yang, Ying,An, Xiao-Ming,Zhou, Yun-Bing,Li, Ren-Hao,Tang, Hai-Tao,Ding, Cheng-Ke,Zhan, Zhuang-Ping
, p. 3936 - 3941 (2016/05/24)
A highly efficient AgOTf catalyzed [3,3] sigmatropic rearrangement/1,3-H shift/6' aza-electrocyclization cascade reaction of N-propargylic hydrazones has been developed. This method provides a new mild synthetic route to various polysubstituted 1,6-dihydr
1-METHYL-BENZO[1,2,4]THIADIAZINE 1-OXIDE DERIVATIVES
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Page/Page column 61-62, (2009/01/20)
The invention is directed to 1-methyl-benzo[1,2,4]thiadiazine 1-oxide derivatives and pharmaceutical compositions containing such compounds that are useful in treating infections by hepatitis C virus.
Synthesis and biological activity of P2-P4 azapeptidomimetic P1-argininal and P1-ketoargininamide derivatives: A novel class of serine protease inhibitors
Sample, J. Edward,Rowley, David C.,Brunck, Terence K.,Ripka, William C.
, p. 315 - 320 (2007/10/03)
Molecular modeling and topographic considerations of the thrombin-specific sequences Boc-Asp-Pro-Arg-TS or Ac-d-Phe-Pro-Arg-TS (TS = transition state analog electrophilic center) and related scaffolds led to the design of novel P2-P4-azapeptidomimetic P1-argininal and P1-ketoargininamide derivatives (3a-j). The synthesis and biological activity of these potential serine protease inhibitors are presented.
