2016
DOI: 10.1002/bkcs.10641
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Synthesis of Arylthiopyrimidines by Copper‐catalyzed Aerobic Oxidative C–S Cross‐coupling

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Cited by 35 publications
(47 citation statements)
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“…The LODs for d ‐fructose or d ‐galactose were not determined. Probe uncapping was explained by the displacement of bulky cyclodextrins by the competitive interaction of monosaccharides with boronic acid moieties . It is also worth mentioning that, despite not having been designed specifically for sensing purposes, other authors have developed selective glucose‐responsive systems, and have used them for the glucose‐induced release of insulin, which was related directly with the amount of glucose present in media …”
Section: Sensing Of Small Neutral Moleculesmentioning
confidence: 99%
“…The LODs for d ‐fructose or d ‐galactose were not determined. Probe uncapping was explained by the displacement of bulky cyclodextrins by the competitive interaction of monosaccharides with boronic acid moieties . It is also worth mentioning that, despite not having been designed specifically for sensing purposes, other authors have developed selective glucose‐responsive systems, and have used them for the glucose‐induced release of insulin, which was related directly with the amount of glucose present in media …”
Section: Sensing Of Small Neutral Moleculesmentioning
confidence: 99%
“…We previously reported the substituent chemical shifts of 2-aryl derivatives of benzimidazole, benzimidazolium ion, and benzimidazolone. 10 However, the carbon atoms of interest were directly bonded to the substituted benzene ring compared to the present systems in which the carbon atoms are separated by an ester group.…”
Section: Articlementioning
confidence: 85%
“…Interestingly, all of the target compounds, except nonacetal derivatives ( 4 ) and synthetic intermediates such as 10‐substituted sulfidylyl ( 6 ) and sulfonyldihydroartemisinin ( 7 ), inhibited angiogenesis, which is a key step in the growth, invasion, and metastasis of tumors, and can be an important therapeutic strategy for cancer and related diseases . Recently, we also reported the synthesis of 10‐substituted triazolyl artemisinins ( 8 ) and their strong cytotoxicity against various cancer cells . Over the course of about 15 years of our novel drug discovery program, we have prepared four types of artemisinin mimic libraries derived from artemisinin as shown in Figure , and using these libraries, we have identified a potential osteoporosis drug candidate.…”
Section: Synthesis Of 10‐exomethylene Artemisinin (9) Using Tebbe Andmentioning
confidence: 99%