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Chemical & Engineering News Archive, 1949 Some of the next articles are maybe not open access.
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ChemInform, 2005
AbstractFor Abstract see ChemInform Abstract in Full Text.
R. D. Larsen, D. Cai
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AbstractFor Abstract see ChemInform Abstract in Full Text.
R. D. Larsen, D. Cai
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Current Medicinal Chemistry, 2010
Although the assortment of antifungal drugs is broad, the most commonly used agents have major drawbacks. Toxicity, serious side effects or the emergence of drug resistance are amongst them. New drugs and drug candidates under clinical trials do not guarantee better pharmacological parameters. These new medicines may appear effective; however; they may
R, Musiol +3 more
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Although the assortment of antifungal drugs is broad, the most commonly used agents have major drawbacks. Toxicity, serious side effects or the emergence of drug resistance are amongst them. New drugs and drug candidates under clinical trials do not guarantee better pharmacological parameters. These new medicines may appear effective; however; they may
R, Musiol +3 more
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Quinoline-Annulated Porphyrins
Organic Letters, 2011Porphyrin-2,3-dione mono- and dioximes were used as starting materials for the efficient syntheses of mono- and bis-quinoline-annulated porphyrins and their corresponding N-oxides. Owing to an extended π-system, these novel porphyrinoid chromophores show significantly red-shifted UV-vis spectra compared to the parent porphyrins.
Joshua, Akhigbe +2 more
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Friedländer quinoline synthesis
2009Also known as the Friedlander condensation, it combines an α-amino aldehyde or ketone with another aldehyde or ketone with at least one methylene α adjacent to the carbonyl to furnish a substituted quinoline. The reaction can be promoted by either acid, base, or heat.
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