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kw.\*:("ACETOHYDROXAMIQUE ACIDE")

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INFLUENCE DES PARTICULARITES DE LA STRUCTURE DES ACIDES HYDROXAMIQUES SUR LEUR DISSOCIATION ET LEUR COMPLEXATIONSHENDEROVICH VA; RYABOJ VI; KRIVELEVA EH D et al.1979; ZH. OBSHCH. KHIM.; SUN; DA. 1979; VOL. 49; NO 8; PP. 1746-1751; BIBL. 23 REF.Article

ACID DISSOCIATION CONSTANTS (KA) AND THEIR TEMPERATURE DEPENDENCIES (DELTA HANDELTA SA) FOR A SERIES OF CARBON- AND NITROGEN-SUBSTITUTED HYDROXAMIC ACIDS IN AQUEOUS SOLUTIONMONZYK B; CRUMBLISS AL.1980; J. ORG. CHEM.; ISSN 0022-3263; USA; DA. 1980; VOL. 45; NO 23; PP. 4670-4675; BIBL. 29 REF.Article

ALLYLIC AMIDATION. AN INVESTIGATION OF NITROSOCARBONYLMETHANE FOR DIRECT ALLYLIC FUNCTIONALIZATION OF OLEFINSKECK GE; YATES JB.1979; TETRAHEDRON LETTERS; GBR; DA. 1979; NO 48; PP. 4627-4630; BIBL. 5 REF.Article

FORMATION DE COMPLEXES DE FEIII AVEC LES DERIVES DE L'ACIDE HYDROXAMIQUESHENDEROVICH VA; STRIZHEV EF; RYABOJ VI et al.1978; ZH. NEORG. KHIM.; SUN; DA. 1978; VOL. 23; NO 10; PP. 2681-2687; BIBL. 23 REF.Article

SYNTHESIS AND REACTIONS OF SOME PARA-SUBSTITUTED N-HYDROXYACETANILIDESCALDER IC; CACIOLLI S.1979; AUSTRAL. J. CHEM.; AUS; DA. 1979; VOL. 32; NO 6; PP. 1301-1306; BIBL. 14 REF.Article

MASS SPECTRA OF SOME N-ARYLACETYLHYDROXAMIC ACIDS, ACETAMIDOPHENOLS AND THEIR METHYL DERIVATIVESDAVIES NW; LENK W; MCLEAN S et al.1982; ORG. MASS SPECTROM.; ISSN 0030-493X; GBR; DA. 1982; VOL. 17; NO 12; PP. 649-651; BIBL. 14 REF.Article

CONVERSION OF NITROSOBENZENE TO N-PHENYLACETOHYDROXAMIC ACID BY YEAST PYRUVATE DECARBOXYLASE. = CONVERSION DU NITROSOBENZENE ET ACIDE N-PHENYLACETOHYDROXAMIQUE PAR LA DECARBOXYLASE PYRUVIQUE DES LEVURESCORBETT MD; CAHOY JE; CHIPKO BR et al.1975; J. NATION. CANCER INST.; U.S.A.; DA. 1975; VOL. 55; NO 5; PP. 1247-1248; BIBL. 6 REF.Article

EFFECT OF ACETOHYDROXAMIC ACID ON RUMEN UREASE ACTIVITY IN VITROMAKKAR HPS; SHARMA OP; DAWRA RK et al.1981; J. DAIRY SCI.; ISSN 0022-0302; USA; DA. 1981; VOL. 64; NO 4; PP. 643-648; BIBL. 23 REF.Article

Acetohydroxamic acids as potent, selective, orally active 5-lipoxygenase inhibitorsJACKSON, W. P; ISLIP, P.J; KNEEN, G et al.Journal of medicinal chemistry (Print). 1988, Vol 31, Num 3, pp 499-500, issn 0022-2623Article

TRANSITION METAL COMPLEXES OF MONOHYDROXAMIC ACIDSBROWN DA; MCKEITH D; GLASS WK et al.1979; INORG. CHIM. ACTA; ITA; DA. 1979; VOL. 35; NO 1; PP. 5-10; BIBL. 20 REF.Article

SYNTHESIS AND ANALYSIS OF GLUCURONIDES OF N-HYDROXYAMIDESFENG PCC; FENSELAU C; COLVIN ME et al.1983; DRUG METABOLISM AND DISPOSITION; ISSN 0090-9556; USA; DA. 1983; VOL. 11; NO 2; PP. 103-108; BIBL. 34 REF.Article

The gas-phase basicity of hydroxamic acid derivativesDECOUZON, M; EXNER, O; GAL, J.-F et al.Journal of organic chemistry. 1992, Vol 57, Num 5, pp 1621-1622, issn 0022-3263Article

N-hydroxy-N-arylacetamides. V: Differences in the mechanism of haemoglobin oxidation in vitro by N-hydroxy-4-chloroacetanilide and N-hydroxy-4-chloroanilineLENK, W; RIEDL, M.Xenobiotica (London. Print). 1989, Vol 19, Num 4, pp 453-475, issn 0049-8254Article

N-HYDROXYAMIDE METABOLITES OF LICOCAINE. SYNTHESIS, CHARACTERIZATION, QUANTITATION, AND MUTAGENIC POTENTIALNELSON SD; NELSON WL; TRAGER WF et al.1978; J. MEDICIN. CHEM.; USA; DA. 1978; VOL. 21; NO 8; PP. 721-725; BIBL. 12 REF.Article

PHOTOMETRIC MICRODETERMINATION OF ACETYL GROUPS IN ORGANIC COMPOUNDSTRUTNOVSKY H; SAKLA AB; ABOU TALEB S et al.1975; MICROCHEM. J.; U.S.A.; DA. 1975; VOL. 20; NO 4; PP. 415-420; BIBL. 10 REF.Article

POTENTIOMETRIC DETERMINATION OF FORMATION CONSTANTS OF METAL CHELATES INVOLVING SOME RARE EARTH METAL IONS AND 2,2'-DIPHENYLACETOHYDROXAMIC ACIDDUBBA REDDY VV; SETHURAM B; NAVANEETH RAO T et al.1981; INDIAN J. CHEM., SECT. A; ISSN 0376-4710; IND; DA. 1981; VOL. 20; NO 11; PP. 1140-1142; BIBL. 4 REF.Article

FURTHER OBSERVATIONS ON THE POTENTIATION OF THE ANTIBACTERIAL EFFECT OF METHENAMINE BY ACETOHYDROXAMIC ACIDMUSHER DM; GRIFFITH DP; TEMPLETON GB et al.1976; J. INFECT. DIS.; U.S.A.; DA. 1976; VOL. 133; NO 5; PP. 564-567; BIBL. 14 REF.Article

INHIBITION OF JACK BEAN UREASE (EC3.5.1.5) BY ACETOHYDROXAMIC ACID AND BY PHOSPHORAMIDATE. AN EQUIVALENT WEIGHT FOR UREASEDIXON NE; GAZZOLA C; WATTERS JJ et al.1975; J. AMER. CHEM. SOC.; U.S.A.; DA. 1975; VOL. 97; NO 14; PP. 4130-4131; BIBL. 23REFArticle

AMINOMETHYLIERUNG VON (ARYLTHIO)- UND (ARYLSULFONYL)-ACETHYDROXAMSAEUREN = AMINOMETHYLATION DES ACIDES (ARYLTHIO)- ET (ARENESULFONYL)-ACETOHYDROXAMIQUESZAYED SMAD; MADIHA FARGHALY.1973; ANN. (JUSTUS LIEBIGS) CHEM.; DTSCH.; DA. 1973; NO 2; PP. 195-200; ABS. ANGL.; BIBL. 6 REF.Serial Issue

REGIOSELEKTIVE ACYLAMINIERUNG DURCH HETERO-COPE-UMLAGERUNG = ACYLATION REGIOSELECTIVE VIA UNE TRANSPOSITION DU TYPE HETERO-COPEHOEFELMEIER R; BLECHERT S.1982; ANGEW. CHEM.; ISSN 0044-8249; DEU; DA. 1982; VOL. 94; NO 5; PP. 375; BIBL. 5 REF.Article

CONVENIENT SYNTHESIS OF SELECTED 14C- AND 3H-LABELED AROMATIC HYDROXYLAMINESTHISSEN MR; ROTH RW; DUNCAN WP et al.1980; ORG. PREP. PROCED. INT.; ISSN 0030-4948; USA; DA. 1980; VOL. 12; NO 6; PP. 337-344; BIBL. 14 REF.Article

Electrochemical studies on haloamides. IV: Reactivity of halocetamides and haloacetohyroxamates toward electrogenerated diethyl malonate anionCASADEI, M. A; DI RIENZO, B; INESI, A et al.Journal of the Chemical Society. Perkin transactions. I. 1992, Num 3, pp 379-382, issn 0300-922XArticle

Molecular structures of caracemide, an inhibitor of ribonucleotide reductase, and of one of its degradation productsKJOÊLLER LARSEN, I.Acta crystallographica. Section C, Crystal structure communications. 1990, Vol 46, pp 600-604, issn 0108-2701, 5 p., part 4Article

The solvolysis of N-acetoxy-1-N-acetylaminonaphthalene and N-acetoxy-2-N-acetylaminonaphthalene: divergent chemistry and mutagenic activityUNDERWOOD, G. R; DAVIDSON, C. M.Journal of the Chemical Society. Chemical communications. 1985, Num 9, pp 555-556, issn 0022-4936Article

Glycosides of N-hydroxy-N-arylamine derivatives. III: Kinetic and mechanistic studies on the degradation reaction of O-glycosides of N-hydroxy-N-arylamines and their acetohydroxamic acids in acidic and alkaline mediaYOSHIOKA, T; UEMATSU, T.Perkin transactions. 2. 1985, Num 9, pp 1377-1381, issn 0300-9580Article

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