cheminform abstract: studies on organophosphorus compounds. part 101. a facile synthetic route to...

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1998 organo-phosphorus compounds, acyclic C derivatives organo-phosphorus compounds, acyclic C derivatives S 0082 27 - 220 Studies on Organophosphorus Compounds. Part 101. A Facile Synthetic Route to Trifluoromethylated Aminophosphonic Acids and Phosphonopeptides. Key step in the synthesis of trifluoromethylated aminophosphonic acid (V) is the Arbuzov rearrangement of imidoyl chlorides (I) with triethylphosphite. Different N-protecting groups are investigated. Coupling reaction of phosphonic acid (V) with a second amino acid moiety gives the protected phosphonopeptides (VII) in relatively low yields. — (YUAN, C.; ZHANG, Y.; LUO, W.; YAO, Z.; Heteroat. Chem. 9 (1998) 2, 139-146; Shanghai Inst. Org. Chem., Acad. Sin., Shanghai 200032, Peop. Rep. China; EN) 1

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Page 1: ChemInform Abstract: Studies on Organophosphorus Compounds. Part 101. A Facile Synthetic Route to Trifluoromethylated Aminophosphonic Acids and Phosphonopeptides

1998 organo-phosphorus compounds, acyclic C derivatives

organo-phosphorus compounds, acyclic C derivativesS 0082

27 - 220Studies on Organophosphorus Compounds. Part 101. A FacileSynthetic Route to Trifluoromethylated Aminophosphonic Acids andPhosphonopeptides. — Key step in the synthesis of trifluoromethylatedaminophosphonic acid (V) is the Arbuzov rearrangement of imidoyl chlorides(I) with triethylphosphite. Different N-protecting groups are investigated.Coupling reaction of phosphonic acid (V) with a second amino acid moiety givesthe protected phosphonopeptides (VII) in relatively low yields. — (YUAN,C.; ZHANG, Y.; LUO, W.; YAO, Z.; Heteroat. Chem. 9 (1998) 2, 139-146;Shanghai Inst. Org. Chem., Acad. Sin., Shanghai 200032, Peop. Rep. China;EN)

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