2017
DOI: 10.1016/j.ejmech.2016.10.035
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Aliphatic and alicyclic camphor imines as effective inhibitors of influenza virus H1N1

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Cited by 43 publications
(24 citation statements)
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“…An interesting series of works on the topic of (+)-camphor-based imine derivatives is presented by Sokolova et al [ 88 , 93 , 94 ]. The authors pointed up a very efficient antiviral activity of synthesized monoterpene derivatives.…”
Section: Monoterpene Bicyclic Derivativesmentioning
confidence: 99%
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“…An interesting series of works on the topic of (+)-camphor-based imine derivatives is presented by Sokolova et al [ 88 , 93 , 94 ]. The authors pointed up a very efficient antiviral activity of synthesized monoterpene derivatives.…”
Section: Monoterpene Bicyclic Derivativesmentioning
confidence: 99%
“…The authors pointed up a very efficient antiviral activity of synthesized monoterpene derivatives. In their 2017 work [ 94 ], designed compounds were prepared from commercially available natural (+)-camphor and various amines ( Figure 24 ), whereas the procedures for the monoterpene derivatives were simple and reproducible. The prepared compounds were tested in vitro for antiviral activity.…”
Section: Monoterpene Bicyclic Derivativesmentioning
confidence: 99%
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“…For example, camphor diimines demonstrate antiviral activity. [9][10][11] Fenchonylamine-based molecules are potential therapeutic agents for the treatment of Alzheimer's disease. [12] Amines are a crucial class of organic compounds with multiple academic and industrial applications.…”
mentioning
confidence: 99%
“…

Photocatalytic selective oxidative coupling of amines is a promisingm ethod for imine synthesis. [2] Therefore, there is increased interest in the synthesis of imines by the hydrogenationo fn itro compounds, [3,4] oxidation and condensation of amines and alcohols, [5,6] and oxidative dehydrogenation of secondary amines. The average apparent quantum efficiency at 455 nm is 57.4 %.

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mentioning
confidence: 99%