UBER DIE SYNTHESE VON 5-PHENYL-1H-THIENO (2,3-E)-1,4-DIAZEPIN-2 (3H)-ONEN = SYNTHESE DE PHENYL-5 1,3H-THIENO (2,3-E) DIAZEPINE-1,4 ONES-2HROMATKA O; BINDER D.1973; MONATSCH. CHEM.; OSTERR.; DA. 1973; VOL. 104; NO 3; PP. 704-708; ABS. ANGL.; BIBL. 6 REF.Serial Issue

UBER DIE NITRODERIVATE VON 5-PHENYL-1H-THIENO-(3,2-E)-1,4-DIAZEPIN-2(3H)-ONEN = DERIVES NITRES DE PHENYL-5 1,3H-THIENO (3,2-E) DIAZEPINE-1,4ONES-2HROMATKA O; BINDER D.1973; MONATSH. CHEM.; OSTERR.; DA. 1973; VOL. 104; NO 4; PP. 1105-1108; ABS. ANGL.; BIBL. 4 REF.Serial Issue

UBER DIE NITRIERUNG VON 7-CHLOR-5-PHENYL-1H-THIENO (2,3-E) 1,4-DIAZEPIN-2 (3H) -ON = NITRATION DE LA CHLORO-7 PHENYL-5 1,3H-THIENO (2,3-E) DIAZEPINE-1,4ONE-2HROMATKA O; BINDER D; STANETTY P et al.1973; MONATSCH. CHEM.; OSTERR.; DA. 1973; VOL. 104; NO 3; PP. 709-714; ABS. ANGL.; BIBL. 4 REF.Serial Issue

UBER DIE SYNTHESE VON SUBSTITUIERTEN THIENO (3,4-B) CHINOLIN-9 (4H)-ONEN = SYNTHESE DE 4H-THIENO (3,4-B) QUINOLEINONES-9HROMATKA O; BINDER D; EICHINGER K et al.1974; MONATSH. CHEM.; OSTERR.; DA. 1974; VOL. 105; NO 6; PP. 1164-1169; ABS. ANGL.; BIBL. 5 REF.Article

UEBER DIE SYNTHESE EINIGER BETA -ALANIN-DERIVATE. = SUR LA SYNTHESE DE QUELQUES DERIVES DE LA BETA -ALANINEHROMATKA O; KNOLLMULLER M; GRAF W et al.1975; MONATOH. CHEM.; OESTERR.; DA. 1975; VOL. 107; NO 4; PP. 889-892; ABS. ANGL.; BIBL. 2 REF.Article

UBER DIE SYNTHESE DES 2,3,4,8-TETRAHYDRO (1) BENZOXEPINO (5,4,3-EF)-1,4-BENZODIAZEPIN-3-ONS. EIN NEUES HETEROCYCLISCHEN RINGSYSTEM = SYNTHESE DE LA TETRAHYDRO-2,3,4,8 BENZOOXEPINNO-1 (5,4,3-EF) BENZODIAZEPINE-1,4ONE-3, UN NOUVEAU SYSTEME HETEROCYCLIQUEHROMATKA O; KNOLLMULLER M; FOROUTAN RAD M et al.1974; MONATSH. CHEM.; OSTERR.; DA. 1974; VOL. 105; NO 5; PP. 1057-1066; ABS. ANGL.; BIBL. 12 REF.Article

UBER DIE SYNTHESE NEUER PYRROL-2-CARBONSAEUREAMIDE = SYNTHESE DE NOUVEAUX PYRROLECARBOXAMIDES-2HROMATKA O; BINDER D; STANETTY P et al.1975; MONATSH. CHEM.; OSTERR.; DA. 1975; VOL. 106; NO 1; PP. 213-218; ABS. ANGL.; BIBL. 3 REF.Article

UBER DIE SYNTHESE VON 4,9-DIHYDRO-9-(2-DIMETHYLAMINO-AETHYL)-4-METHYL-THIENO (3,4-B) (1,5) BENZODIAZEPIN-10-ON. EINE DEM DIBENZEPIN ANALOGE THIOPHENVERBINDUNG = SYNTHESE DE DIHYDRO-4,9 (DIMETHYLAMINO-2 ETHYL)-9 METHYL-4 THIENO (3,4-B) BENZODIAZEPINE-1,5 ONE-10, UN DERIVE DU THIOPHENE ANALOGUE DE LA DIBENZEPINEHROMATKA O; BINDER D; EICHINGER K et al.1975; MONATSH. CHEM.; OSTERR.; DA. 1975; VOL. 106; NO 2; PP. 375-379; ABS. ANGL.; BIBL. 4 REF.Article

UBER DIE SYNTHESE VON 6,7-DICHLOR-5-PHENYL-1H-THIENO-(2,3-E)-1,4-DIAZEPIN-2(3H)-ON = SYNTHESE DE LA DICHLORO-6,7 PHENYL-5 1,3H-THIENO (2,3-E) DIAZEPINE-1,4ONE-2HROMATKA O; BINDER D; STANETTY P et al.1973; MONATSH. CHEM.; OSTERR.; DA. 1973; VOL. 104; NO 4; PP. 920-924; ABS. ANGL.; BIBL. 4 REF.Serial Issue

UBER DIE SYNTHESE VON 7-METHOXYCARBONYL-5-PHENYL-1H-THIENO (2,3-E) 1,4-DIAZEPIN-2 (3H)-ON = SYNTH. DE METHOXYCARBONYL-7 PHENYL-5 1,3H-THIENO (2,3-E) DIAZEPINE-1,4ONE-2HROMATKA O; BINDER D; VEIT W et al.1973; MONATSH. CHEM.; OSTERR.; DA. 1973; VOL. 104; NO 4; PP. 973-978; ABS. ANGL.; BIBL. 3 REF.Serial Issue

THIOPHENALS STRUKTURELEMENT PHYSIOLOGISH AKTIVER SUBSTANZEN. IV: O-SUBSTITUIERTE 5-PHENYL-THIENO (2,3-E) (1,4) DIAZEPINE = LE THIOPHENE EN TANT QU'ELEMENT STRUCTURAL DE SUBSTANCES BIOLOGIQUEMENT ACTIVES. IV: PHENYL-5 THIENO (2,3-E) DIAZEPINES-1,4 O-SUBSTITUEESBINDER D; HROMATKA O; NOE CR et al.1980; ARCH. PHARM.; DEU; DA. 1980; VOL. 313; NO 7; PP. 587-602; ABS. ENG; BIBL. 12 REF.Article

THIOPHEN ALS STRUKTURELEMENT PHYSIOLOGISCH AKTIVER SUBSTANZEN. V: 5-O-NITROPHENYL-SUBSTITUIERTE THIENO (2,3-E) (1,4) DIAZEPINE = LE THIOPHENE EN TANT QU'ELEMENT STRUCTURAL DE SUBSTANCES BIOLOGIQUEMENT ACTIVES. V: THIENO (2,3-E) DIAZEPINES-1,4 O-NITROPHENYL-5 SUBSTITUEESBINDER D; HROMATKA O; NOE CR et al.1980; ARCH. PHARM.; DEU; DA. 1980; VOL. 313; NO 7; PP. 636-644; ABS. ENG; BIBL. 2 REF.Article

Analogues and derivatives of tenoxicam. I: Synthesis and antiinflammatory activity of analogues with different residues on the ring nitrogen and the amide nitrogenBINDER, D; HROMATKA, O; GEISSLER, F et al.Journal of medicinal chemistry (Print). 1987, Vol 30, Num 4, pp 678-682, issn 0022-2623Article