Fuente: PubMed "apis" Curr Org Synth. 2026 Jul 25. doi: 10.2174/0115701794488864260713064630. Online ahead of print.ABSTRACTThe growing demand for efficient, selective, and environmentally friendly strategies to construct biologically relevant molecules has driven continuous innovation in coupling and condensation reagents. Among these, n-propylphosphonic anhydride (T3P®) has emerged as a versatile and green reagent for a wide range of bond-forming transformations. Recognized as an environmentally benign alternative to traditional agents such as DCC, EDC, and CDI, T3P® operates under mild conditions, minimizes racemization, and generates water-soluble byproducts that are easily removable. Its prominent application in amide and peptide coupling reactions has made it indispensable in medicinal chemistry and the synthesis of active pharmaceutical ingredients (APIs), delivering high yields with minimal epimerization in both solution- and solid-phase peptide synthesis. This review comprehensively covers T3P®-facilitated synthesis of diverse amides, including N-acyl tryptamines, N-acyl α-cyanoamines, cyanoaryl amides, N-acyl cyanoarylamines, o-ureidobenzonitriles, N-substituted amides, α-amino amides, N-acyl-benzotriazoles, dialkylamides, and N-formyl-imides. Beyond peptide chemistry, T3P® has proven effective for carboncarbon and carbon-heteroatom bond formation, as well as for condensation reactions via one-, two-, and three-component protocols. Representative transformations include the synthesis of αaminonitriles, 1-carbamatoalkyl 2-naphthols, and 3,4-dihydropyrimidin-2(1H)-ones/thiones via three-component reactions; isothiocyanates,β-enaminones, N-alkenylated heterocycles, β-amino ketones, N-(acyloxy)phthalimides, indole-based triarylmethanes, syn-diacetoxylated cinnamic esters, and aromatic aldehydes via two-component protocols; and nitriles via one-component protocols. By summarizing mechanistic insights, reaction scope, and emerging applications, this review underscores T3P® as a versatile, operationally simple, and environmentally conscious reagent for constructing structurally diverse and pharmaceutically relevant molecules in modern organic synthesis. In this paper, we provide an updated ten-year overview (2015-present), emphasizing T3P®'s versatility as a reagent in various bond-forming reactions.PMID:42522306 | DOI:10.2174/0115701794488864260713064630