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NOVEL CONVERSION OF PENICILLINS INTO CEPHALOSPORINSNAYLER JHC; PEARSON MJ; SOUTHGATE R et al.1973; J. CHEM. SOC., CHEM. COMMUNIC.; G.B.; DA. 1973; NO 2; PP. 58-59; BIBL. 6 REF.Serial Issue

BEITRAGE ZUR CHEMIE DER BETA -LACTAM-ANTIBIOTIKA = CHIMIE DES BETA -LACTAMES ANTIBIOTIQUESGOSTELI J.1976; CHIMIA; SUISSE; DA. 1976; VOL. 30; NO 1; PP. 13-14; ABS. ANGL.; BIBL. 3 REF.Article

A STEREOSELECTIVE OXIDATIVE CYCLIZATION OF D-MANDELAMIDO-3-CARBAMOYLOXYMETHYL-3-CEPHEM-4-CARBOXYLIC ESTERKOPPEL GA; KOEHLER RE.1973; TETRAHEDRON LETTERS; G.B.; DA. 1973; NO 22; PP. 1943-1946; BIBL. 1 P.Serial Issue

TRANSFORMATION OF PENICILLIN SULPHOXIDES INTO CEPHALOSPORINS BY AZO-COMPOUNDSTERAO S; MATSUO T; TSUSHIMA S et al.1972; J. CHEM. SOC., CHEM. COMMUNIC.; G.B.; DA. 1972; NO 23; PP. 1304-1305; BIBL. 2 REF.Serial Issue

ALKYLATION OF CEPHEM COMPOUNDSOIDA S; YOSHIDA A; OHKI E et al.1975; ANNU. SANKYO RES. LAB.; JAP.; DA. 1975; VOL. 27; PP. 53-63; ABS. JAP.; BIBL. 6 REF.Article

3-ACYLOXYMETHYL-7-(2-THIENYLACETAMIDO)-3-CEPHEM-4-CARBOXYLIC ACIDS. AN IMPROVED SYNTHESIS AND BIOLOGICAL PROPERTIESBERGES DA.1975; J. MEDICIN. CHEM.; U.S.A.; DA. 1975; VOL. 18; NO 12; PP. 1264-1265; BIBL. 9 REF.Article

TOTAL SYNTHESIS OF BETA -LACTAM ANTIBIOTICS. V. ( +OU- )-3'-METHYLCEPHALOTHINSTEINBERG NG; RATCLIFFE RW; CHRISTENSEN BG et al.1974; TETRAHEDRON LETTERS; G.B.; DA. 1974; NO 40; PP. 3567-3570; BIBL. 8 REF.Article

MODIFIKATIONEN VON ANTIBIOTICA. XII. NEUE BETA -LACTAM-ANTIBIOTIKA. UBER DIE DARSTELLUNG UND DECARBONYLIERUNG VON 3-FORMYLCEPHEM-VERBINDUNGEN = MODIFICATIONS DES ANTIBIOTIQUES. XII. NOUVEAUX BETA -LACTAMES ANTIBIOTIQUES. PREPARATION ET DECARBONYLATION DE FORMYL-3 CEPHEMESPETER H; BICKEL H.1974; HELV. CHIM. ACTA; SUISSE; DA. 1974; VOL. 57; NO 7; PP. 2044-2054; ABS. ANGL.; BIBL. 15 REF.Article

MODIFIKATIONEN VON ANTIBIOTIKA. X. NEUE BETA -LACTAM-ANTIBIOTIKA. UBER DERIVATE DER 3-HYDROXY-7-AMINO-CEPH-3-EM-4-CARBONSAEURE = MODIFICATIONS DES ANTIBIOTIQUES. X. NOUVEAUX BETA -LACTAMES ANTIBIOTIQUES. DERIVES DE L'ACIDE HYDROXY-3 AMINO-7 CEPHEME-3 CARBOXYLIQUE-4SCARTAZZINI R; BICKEL H.1974; HELV. CHIM. ACTA; SUISSE; DA. 1974; VOL. 57; NO 7; PP. 1919-1934; ABS. ANGL.; BIBL. 9 REF.Article

THE PREPARATION AND USE OF 4-PHENYLTHIAZOLIDINE-2,5-DIONE IN THE SYNTHESIS OF 7-(D-2-AMINO-3-PHENYLACETAMIDO)-3-METHYL-3-CEPHEM-4-CARBOXYLIC ACID (CEPHALEXIN).JAPELJ M; VITEZIC N; HOHNJEC M et al.1978; DOCUM. CHEM. YUGOSL.; YOUGOSL.; DA. 1978; VOL. 25; NO 1; PP. 13-30; ABS. SOLVENE; BIBL. 2 P.Article

THE CHEMISTRY OF CEPHAMYCINS. V. THE REACTIONS OF THE CARBAMOYL GROUP.KARADY S; WEINSTOCK LM; ROBERTS FE et al.1976; TETRAHEDRON LETTERS; G.B.; DA. 1976; NO 28; PP. 2401-2404; BIBL. 8 REF.Article

TOTAL SYNTHESIS OF BETA -LACTAM ANTIBIOTICS. VI. 3-ACRYLCEPHALOSPORINSFIRESTONE RA; MACIEJEWICZ NS; CHRISTENSEN BG et al.1974; J. ORG. CHEM.; U.S.A.; DA. 1974; VOL. 39; NO NO 23; PP. 3384-3387; BIBL. 15 REF.Article

CHEMISTRY OF CEPHALOSPORIN ANTIBIOTICS. XXIX. 3-HALO- AND 3-METHOXY-3-CEPHEMSCHAUVETTE RR; PENNINGTON PA.1974; J. AMER. CHEM. SOC.; U.S.A.; DA. 1974; VOL. 96; NO 15; PP. 4986-4987; BIBL. 9 REF.Article

SYNTHESIS OF C7 ALKYLATED 7-DEAMINOCEPHALOSPORIN DERIVATESWIERING JS; WYNBERG H.1976; J. ORG. CHEM.; U.S.A.; DA. 1976; VOL. 41; NO 9; PP. 1574-1578; BIBL. 21 REF.Article

PREPARATION OF A NOVEL CEPHALOSPORIN SULFONIUM SALTHERRON DK.1975; TETRAHEDRON LETTERS; G.B.; DA. 1975; NO 26; PP. 2145-2148; BIBL. 9 REF.Article

SYNTHETIC STUDIES IN THE FIELD OF NATURAL PRODUCTSKISHI Y.1975; PURE APPL. CHEM.; G.B.; DA. 1975; VOL. 43; NO 3-4; PP. 423-438; BIBL. 17 REF.; (INT. CONF. ORG. SYNTH. 1; LOUVAIN-LA-NEUVE; 1974)Conference Paper

MODIFIKATIONEN VON ANTIBIOTIKA. XIII. NEUE BETA -LACTAM-ANTIBIOTIKA. UBER DIE FUNKTIONALISIERUNG DER CEPHEM-3-STELLUNG MITTELS SCHWEFEL ODER STICKSTOFF = MODIFICATIONS D'ANTIBIOTIQUES. XIII. NOUVEAUX BETA -LACTAMES ANTIBIOTIQUES. FONCTIONNALISATION DE LA POSITION 3 DU CEPHEME AVEC LE SOUFRE OU L'AZOTESCARTAZZINI R; SCHNEIDER P; BICKEL H et al.1975; HELV. CHIM. ACTA; SUISSE; DA. 1975; VOL. 58; NO 8; PP. 2437-2450; ABS. ANGL.; BIBL. 8 REF.Article

MODIFIKATIONEN VON ANTIBIOTIKA. XIV. NEUE BETA -LACTAM-ANTIBIOTIKA. CEPHEM-DERIVATE MIT ELEKTRONENANZIEHENDEN SUBSTITUENTEN IN 3-STELLUNG = MODIFICATIONS D'ANTIBIOTIQUES. XIV. NOUVEAUX BETA -LACTAMES ANTIBIOTIQUES. DERIVES DE CEPHEME AVEC DES SUBSTITUANTS ATTRACTEURS D'ELECTRONS EN POSITION 3PETER H; MULLER B; BICKEL H et al.1975; HELV. CHIM. ACTA; SUISSE; DA. 1975; VOL. 58; NO 8; PP. 2450-2469; ABS. ANGL.; BIBL. 16 REF.Article

SYNTHESE VON CEPHEM-4-CARBONSAEUREN = SYNTHESE D'ACIDES CEPHEMECARBOXYLIQUES-4BORMANN D.1974; ANN. (JUSTUS LIEBIGS) CHEM.; DTSCH.; DA. 1974; NO 9; PP. 1391-1398; ABS. ANGL.; BIBL. 6 REF.Article

SYNTHESE VON DESACETOXYCEPHALOSPORIN-S-OXIDEN AUS PENICILLIN-S-OXIDEN DURCH OXIDATIVEN EINFANG DER INTERMEDIAER ENTSTANDENEN SULFENSAEURE-GRUPPIERUNG = SYNTHESE DES S-OXYDES DE DESACETOXYCEPHALOSPORINE A PARTIR DES S-OXYDES DE PENICILLINE PAR FIXATION OXYDANTE DU GROUPEMENT DE L'ACIDE SULFENIQUE INTERMEDIAIREKUKOLJA S; LAMMERT SR.1973; ANGEW. CHEM.; DTSCH.; DA. 1973; VOL. 85; NO 1; PP. 40-41; BIBL. 12 REF.Serial Issue

SYNTHESIS OF 2-METHYL-3-CEPHEM DERIVATIVESKAMIYA T; TERAJI T; HASHIMOTO M et al.1976; J. AMER. CHEM. SOC.; U.S.A.; DA. 1976; VOL. 98; NO 8; PP. 2342-2344; BIBL. 13 REF.Article

A NOVEL SYNTHESIS OF 7-METHOXYCEPHALOSPORINS AND 6-METHOXYPENICILLINSSUGIMURA Y; IINO K; IWANO Y et al.1976; TETRAHEDRON LETTERS; G.B.; DA. 1976; NO 16; PP. 1307-1310; BIBL. 5 REF.Article

TRANSFORMATION OF PENICILLIN SULFOXIDE ESTER INTO 2-HALOGEN-SUBSTITUTED PENICILLIN ESTER, INTERMEDIATE TO CEPHAM SYSTEMTANIDA H; TSUJI T; TSUSHIMA T et al.1975; TETRAHEDRON LETTERS; G.B.; DA. 1975; NO 38; PP. 3303-3306; BIBL. 10 REF.Article

SEMISYNTHETIC CEPHALOSPORINS. SYNTHESIS AND STRUCTURE-ACTIVITY RELATIONSHIPS OF 7-SULFONYLACETAMIDO-3-CEPHEM-4-CARBOXYLIC ACIDSDEMARINIS RM; HOOVER JRE; LAM LL et al.1976; J. MEDICIN CHEM.; U.S.A.; DA. 1976; VOL. 19; NO 6; PP. 754-759; BIBL. 7 REF.Article

THE CONVERSION OF PENICILLIN S-OXIDES INTO CEPHALOSPORIN S-OXIDESISHIMARU T; IMAMOTO T.1975; BULL. CHEM. SOC. JAP.; JAP.; DA. 1975; VOL. 48; NO 10; PP. 2989-2990Article

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