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Palabras clave – provistas por la editorial

amine nucleophiles; alkynoic acids; cascade reaction; gold catalysis; fused N-heterocycles; solid-phase synthesis; ketone; traceless synthesis; natural products; enol ethers; photocatalysis; photoredox; visible-light-induced catalysis; photoredox cyclization; organic dyes; heterocycles; dihydrocoumarins; synthesis; 3-trifluoroacetyl coumarins; phenols; antifungal activities; terpyridines; 3,2′:6′,3″-terpyridine; cyclohexanol derivative; condensation; heterocyclic; 1,2,3-triazol; triazolylmethyl phosphinate; triazolylmethyl phosphate; copper-catalyzed azide-alkyne cycloaddition; click reaction; azides; cinnolines; triazoles; CuAAC; alkynes; cycloalkynes; Richter cyclization; Suzuki coupling; fluorescence; cytotoxicity; coumarin; pyrazolo[3,4-b]pyridine; silica sulfuric acid; 2H-pyran; valence isomerism; 1-oxa-triene; dienone; oxa-electrocyclization; Knoevenagel; propargyl Claisen; cycloisomerization; asymmetric dimeric β-carboline; acylhydrazone group; cytotoxic; antitumor; structure–activity relationship; γ-lactam; pyrrolidones; multicomponent reactions; organocatalysis; pyridine; CF3CO-acetylenes; 1,3-oxazines; fluorinated heterocycles; saturated oxygen heterocycles; cyclic ethers; total synthesis; multicomponent reaction; α-halohydrazones; Staudinger reaction; aza-Wittig; 1H-imidazole-2(3H)-thione; 2H-imidazo[2,1-b][1,3,4]thiadiazine; purine; nucleobase; aromatic substitution; arylation; fluoroalcohol; α-chloroglycinates; 5-acylamino-1,3-thiazoles; Hantzsch reaction; TMSBr; propargylic alcohols; cascade cyclization; 4-bromo quinolines; synthesis of benzofurans; intra-molecular approach; inter-molecular approach; n/a