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Palabras clave – provistas por la editorial

phosphonium salts; N-acyliminium cations; α-amidoalkylation; α-amidoalkylating agents; ylides; Wittig reaction; α-aminophosphonates; α-aminophosphinates; α-aminophosphine oxides; rare earth elements; actinoids; separation; recovery; extraction; precipitation; α-aminobisphosphonates; α-ethoxyphosphonates; N-acylimidates; Michaelis–Becker reaction; Michaelis–Arbuzov reaction; betulin; triphenylphosphonium cation; anticancer; antibacterial activity; osteoporosis; bisphosphonates; zoledronate; metal phosphonates; hybrid materials; controlled release; MOFs; strontium; barium; acene; anthracene; phosphine; phosphonate; phosphonium salt; phosphorane; phosphate; diphosphene; tri-, tetra-, pentacoordinated phosphorus; properties; HWE reaction; Still-Gennari olefination; Ando olefination; stereoselective synthesis; Z-selectivity; phosphonates; alkenes; hexafluoroisopropanol; C=C bond formation; Reformatsky reaction; tetrasubstituted α-aminophosphonates; aspartic acid; antiproliferative effect; diazotization; carbenium ion; 1-phosphonoalkylium ion; substitution reaction; elimination reaction; rearrangement; aminophosphonates; heteroaromatic; lithiation; phosphonylation; phosphonic acids; organophosphorus chemistry; P-containing drugs; n/a