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Studies on organophosphorus compounds 65, a facile synthetic route to phosphonopeptidesCHENGYE YUAN; GUOHONG WANG.Phosphorus, sulfur and silicon and the related elements (Print). 1992, Vol 71, Num 1-4, pp 207-212, issn 1042-6507Article

Induction of an antibody that catalyzes the hydrolysis of an amide bondJANDA, K. D; SCHLOEDER, D; BENKOVIC, S. J et al.Science (Washington, D.C.). 1988, Vol 241, Num 4870, pp 1188-1191, issn 0036-8075Article

Phosphonamidate inhibitors of human neutrophil collagenaseMOOKHTIAR, K. A; MARLOWE, C. K; BARTLETT, P. A et al.Biochemistry (Easton). 1987, Vol 26, Num 7, pp 1962-1965, issn 0006-2960Article

Potent inhibition of endopeptidase 24.16 and endopeptidase 24.15 by the phosphonamide peptide N-(phenylethylphosphonyl)-Gly-L-Pro-L-aminohexanoic acidBARELLI, H; DIVE, V; YIOTAKIS, A et al.Biochemical journal (London. 1984). 1992, Vol 287, pp 621-625, issn 0264-6021, 2Article

Conversions of the adducts of α-dichloronitrosoalkanes with dichlorophosphinesLYASHENKO, YU. E; SOKOLOV, V. B; MARTYNOV, I. V et al.Phosphorus, sulfur and silicon and the related elements (Print). 1991, Vol 60, Num 1-2, pp 85-95, issn 1042-6507, 11 p.Article

Stereoelectronic control in the base catalyzed hydrolysis of five-membered ring cyclic phosphonamidatesJI-CHARNG YANG; GORENSTEIN, D. G.Tetrahedron letters. 1984, Vol 25, Num 41, pp 4627-4630, issn 0040-4039Article

Utilisation de dérivés phosphorés chiraux en synthèse asymétrique = Application of chiral phosphonamides in asymmetric synthesisSabelle, Stéphane; Alexakis, Alexandre.1996, 317 p.Thesis

A novel rearrangement reaction accompanying alkyl metaphosphate extrusion on low-temperature photolysis of 2,3-oxaphosphabicyclo[2.2.2]octene derivativesQUIN, L. D; WU, X.-P; LUKES, I et al.Tetrahedron letters. 1992, Vol 33, Num 28, pp 3975-3978, issn 0040-4039Article

N, O-bis(diphenylphosphinoyl)hydroxylamine base-induced rearrangement to a phosphonamidic-phosphinic mixed anhydridHARGER, M. J. P.Tetrahedron letters. 1990, Vol 31, Num 10, pp 1451-1454, issn 0040-4039Article

Tight binding inhibitors of N-acyl amino sugar and N-acyl amino acid deacetylasesCHENGFU XU; HALL, Richard; CUMMINGS, Jennifer et al.Journal of the American Chemical Society. 2006, Vol 128, Num 13, pp 4244-4245, issn 0002-7863, 2 p.Article

Base-induced rearrangement of N-[benzyl(isopropyl)-phosphinoyl]-O-p-nitrophenylsulfonylhydroxylamine: relative migratory aptitudes of benzyl and isopropylHARGER, M. J. P.Journal of chemical research. Synopses (Print). 1993, Num 5, pp 176-177, issn 0308-2342Article

New catalysts containing an N-P=O structural unit for the asymmetric reduction of ketonesBURNS, B; STUDLEY, J. R; WILLS, M et al.Tetrahedron letters. 1993, Vol 34, Num 44, issn 0040-4039, 6966, 7105-7106 [3 p.]Article

Bisphosphonates. VI: Methylenebisphosphonic acid partial esters and amidesPOHJALA, E; NUPPONEN, H; VEPSÄLÄINEN, J et al.Phosphorus, sulfur and silicon and the related elements (Print). 1993, Vol 76, Num 1-4, pp 159-162, issn 1042-6507Conference Paper

Peptide sequencing through N-terminal phosphonylation and electrospray ionization mass spectrometryJIANGYIN BAO; HUIWANG AI; HUA FU et al.Journal of mass spectrometry. 2005, Vol 40, Num 6, pp 772-776, issn 1076-5174, 5 p.Article

Synthesis and stability studies of phosphonoformate-amino acid conjugates: a new class of slowly releasing foscarnet prodrugsMARMA, Mong S; KASHEMIROV, Boris A; MCKENNA, Charles E et al.Bioorganic & medicinal chemistry letters (Print). 2004, Vol 14, Num 7, pp 1787-1790, issn 0960-894X, 4 p.Article

A convenient synthetic approach to new α-(9-fluorenylmethoxycarbonylamino)alkylphosphonic acid derivativesDUMY, P; ESCALE, R; GIRARD, J. P et al.Synthesis (Stuttgart). 1992, Num 12, pp 1226-1228, issn 0039-7881Article

Time-dependent inhibition of Streptococcus faecalis D-alanine: D-alanine ligase by α-aminophosphonamidic acidsLACOSTE, A. M; CHOLLET-GRAVEY, A. M; VO QUANG, L et al.European journal of medicinal chemistry. 1991, Vol 26, Num 3, pp 255-260, issn 0223-5234, 6 p.Article

Evaluation of intrinsic binding energy from a hydrogen bending group in an enzyme inhibitorBARTLETT, P. A; MARLOWE, C. K.Science (Washington, D.C.). 1987, Vol 235, Num 4788, pp 569-571, issn 0036-8075Article

Effect of basicity on the decomposition of the conjugate base of 4-nitrophenyl N-aryl-P-phenylphosphonamidatesBOURNE, N; WILLIAMS, A.Perkin transactions. 2. 1985, Num 2, pp 265-268, issn 0300-9580Article

Synthèse d'haptènes phosphonamidiques en vue d'une production d'anticorps protéasiques = Phosphonamidic haptens synthesis in the aim of protease antibodies productionLafon Maffre, Dominique; Escale, R.1994, 203 p.Thesis

Lossen-like rearrangement of N-[α-methylbenzyl(phenyl)phosphinoyl]-O-methylsulfonylhydroxylamine with methylamine : retention of configuration at phosphorus as revealed by X-ray crystallographyFAWCETT, J; HARGER, M. J. P; RAMESH SREEDHARAN-MENON et al.Journal of the Chemical Society. Chemical communications. 1992, Num 3, pp 227-229, issn 0022-4936Article

Influence of ortho methyl and isopropyl substituents on the reactivity of N-t-butyl P-arylphosphonamidic chlorides with isopropylamine and t-butylamine: steric acceleration of metaphosphonimidate formation by an elimination-addition mechanism; contrasting behaviour of N,N-dimethyl P-arylphosphonamidic chloridesFREEMAN, S; HARGER, M. J. P.Journal of the Chemical Society. Perkin transactions. I. 1987, Num 6, pp 1399-1406, issn 0300-922XArticle

Structures of two thermolysin-inhibitor complexes that differ by a single hydrogen bondTRONRUD, D. E; HOLDEN, H. M; MATTHEWS, B. W et al.Science (Washington, D.C.). 1987, Vol 235, Num 4788, pp 571-574, issn 0036-8075Article

Synthesis and biological evaluation of phosphonamidate peptide inhibitors of enkephalinase and angiotensin-converting enzymeELLIOTT, R. L; MARKS, N; BERG, M. J et al.Journal of medicinal chemistry (Print). 1985, Vol 28, Num 9, pp 1208-1216, issn 0022-2623Article