2 research outputs found

    A novel and chemoselective process of N-alkylation of aromatic nitrogen compounds using quaternary ammonium salts as starting material

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    ArtĂ­culo Internacional Open AccesThe process of N-alkylation of several pyrroles, indoles, and derivative heterocycles is herein described, using quaternary ammonium salts as the source of an alkylating agent. These reactions were carried out on several heterocyclic rings with triethylbenzylammonium chloride or tetradecyltrimethyl ammonium bromide and an NaOH solution at 50%, leading to a chemoselective N-alkylated product and an average yield of 73%. This is an alternative process to the traditional benzylation and methylation of N-heterocycles with direct handling of alkyl halides.CONACYT, SecretarĂ­a de InvestigaciĂłn y Estudios Avanzados de la UAE

    Synthesis and antifungal activity of novel oxazolidin-2-one linked-1,2,3-triazole derivatives

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    ArtĂ­culo IndizadoNovel oxazolidin-2-one-linked 1,2,3-triazole derivatives (4a–k) were synthesized by straightforward and versatile azide–enolate (3 + 2) cycloaddition. The series of compounds was screened for antifungal activity against four filamentous fungi as well as six yeast species of Candida spp. According to their efficiency and breadth of scope, they can be ordered as 4k > 4d > 4h > 4a, especially in relation to the activity displayed against Candida glabrata ATCC-34138, Trichosporon cutaneum ATCC-28592 and Mucor hiemalis ATCC-8690, i.e. compounds 4d, 4h and 4k showed excellent activity against C. glabrata (MIC 0.12, 0.25 and 0.12 ÎŒg mL−1, respectively), better than that of itraconazole (MIC 1 ÎŒg ml−1). The activity of compound 4d (MIC = 2 ÎŒg mL− 1) was higher than that observed for the standard antifungal drug (MIC = 8 ÎŒg mL−1) against Trichosporon cutaneum, while compound 4k displayed an excellent antimycotic activity against Mucor hiemalis (MIC = 2 ÎŒg mL−1 vs. 4 ÎŒg mL−1 for itraconazole). In addition, we describe herein a novel mild and eco-friendly synthetic protocol for obtaining ÎČ-ketosulfones (adducts to afford compounds 4a–k) from α-brominated carbonyls in an aqueous nanomicellar medium at room temperature.CONACYT, SecretarĂ­a de InvestigaciĂłn de Estudios Avanzados de la UAE
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