64037-16-7Relevant academic research and scientific papers
INHIBITORS OF HEPATITIS C VIRUS REPLICATION
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Paragraph 0912-0913, (2019/05/15)
The present invention relates to compounds of formula (I) that are useful as hepatitis C virus (HCV) NS5A inhibitors, the synthesis of such compounds, and the use of such compounds for inhibiting HCV NS5A activity, for treating or preventing HCV infections and for inhibiting HCV viral replication and/or viral production in a cell-based system.
Cyanoguanidine as a versatile, eco-friendly and inexpensive reagent for the synthesis of 2-aminobenzoxazoles and 2-guanidinobenzoxazoles
Grytsai, Oleksandr,Druzhenko, Tetiana,Demange, Luc,Ronco, Cyril,Benhida, Rachid
supporting information, p. 1642 - 1645 (2018/03/29)
An effective, easy-to-handle, safe and inexpensive protocol is reported for the synthesis of 2-aminobenzoxazoles under Lewis acid activation, utilising cyanoguanidine as the cyanating reagent. An optimized procedure for the synthesis of 2-guanidinobenzoxazole and novel derivatives is also described.
INHIBITORS OF HEPATITIS C VIRUS REPLICATION
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Page/Page column 149, (2010/11/04)
The present invention relates to compounds of formula (I) that are useful as hepatitis C virus (HCV) NS5A inhibitors, the synthesis of such compounds, and the use of such compounds for inhibiting HCV NS5A activity, for treating or preventing HCV infections and for inhibiting HCV viral replication and/or viral production in a cell-based system.
Formation of nitrogen-containing heterocycles using di(imidazole-1-yl)methanimine
Wu, Yong-Qian,Limburg, David C.,Wilkinson, Douglas E.,Hamilton, Gregory S.
, p. 191 - 193 (2007/10/03)
A mild and efficient synthesis of five- and six-membered nitrogen containing heterocyclic compounds, in which di(imidazole-1-yl)methanimine serves as a one-carbon source, is reported.
Approach to the synthesis of (+)-ifforestine. Model studies directed at the tetracyclic framework
Roos, Gregory H. P.,Dastlik, Kim A.
, p. 2023 - 2044 (2007/10/03)
In order to design an effective asymmetric synthesis of (+)-ifforestine, model approaches to the construction of the tetracyclic ring system have been investigated. These studies have identified two key synthons, a functionalized isatoic anhydride and a p
