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ARYNIC CONDENSATION OF KETONES ENOLATES. XIV: CONDENSATION OF AROMATIC ALPHA ,BETA -UNSATURATED KETONE ENOLATES ON ARYNESESSIZ M; GUILLAUMET G; CAUBERE P et al.1979; TETRAHEDRON; GBR; DA. 1979; VOL. 35; NO 9; PP. 1167-1171; BIBL. 15 REF.Article

ARYNIC CONDENSATIONS OF KETONE ENOLATES. XV: NEW SYNTHETIC APPLICATIONS OF THE CONDENSATION OF ALPHA ,BETA -UNSATURATED KETONE ENOLATES ON BENZYNEESSIZ M; GUILLAUMET G; BRUNET JJ et al.1980; J. ORG. CHEM.; USA; DA. 1980; VOL. 45; NO 2; PP. 240-246; BIBL. 28 REF.Article

ARYNIC CONDENSATION OF ALPHA BETA -UNSATURATED KETONE ENOLATESESSIZ M; GUILLAUME G; BRUNET JJ et al.1979; J. CHEM. SOC., CHEM. COMMUNIC.; GBR; DA. 1979; NO 6; PP. 276-277; BIBL. 4 REF.Article

Amino-3 penams et dérivés. Synthèse et évaluation biologique = 3-Aminopenams and derivatives: synthesis and biological activityBOUZARD, D; ESSIZ, M; REMUZON, P et al.European journal of medicinal chemistry. 1983, Vol 18, Num 5, pp 405-411, issn 0223-5234Article

Synthesis of (1R,4R,7S)- and (1S,4S,7S)-2-(4-tolylsylfonyl)-5-phenyl-methyl-7-methyl-2,5-diazabicyclo[2.2.1]heptanes via regioselective opening of 3,4-epoxy-D-proline with lithium dimethyl cuprateESSIZ, M; JACQUET, J.-P; CLEMENCIN, C et al.ESSIZ, M; JACQUET, J.-P; Journal of heterocyclic chemistry. 1993, Vol 30, Num 2, pp 517-523, issn 0022-152XArticle

Utilisation du fluorure de tétrabutylammonium comme agent de cyclisation dans la synthèse d'antibactériens dérivés d'acide pyridone-4-carboxylique-3 = Utilization of tetrabutylammonium fluoride as cyclization agent in the synthesis of antibacterial 4-pyridone-3-carboxylic acid derivativesBOUZARD, D; DI CESARE, P; ESSIZ, M et al.Tetrahedron letters. 1988, Vol 29, Num 16, pp 1931-1934, issn 0040-4039Article

Fluoronaphthyridines as antibacterial agents. IV: Synthesis and structure-activity relationships of 5-substituted-6-fluoro-7-(cycloalkylamino)-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acidsBOUZARD, D; DI CESARE, P; ESSIZ, M et al.Journal of medicinal chemistry (Print). 1992, Vol 35, Num 3, pp 518-525, issn 0022-2623Article

Fluoronaphthyridines and quinolones as antibacterial agents. I: Synthesis and structure-activity relationships og new 1-substituted deivativesBOUZARD, D; DI CESARE, P; ESSIZ, M et al.Journal of medicinal chemistry (Print). 1989, Vol 32, Num 3, pp 537-542, issn 0022-2623, 6 p.Article

Fluoronaphthyridines and -quinolones as antibacterial agents. V: Synthesis and antimicrobial activity of chiral 1-tert-butyl-6-fluoro-7-substituted-naphthyridonesDI CESARE, P; BOUZARD, D; ESSIZ, M et al.Journal of medicinal chemistry (Print). 1992, Vol 35, Num 22, pp 4205-4213, issn 0022-2623Article

Fluoronaphthyridines and quinolones as antibacterial angents. II, Synthesis and structure-activity relationships of new 1-tert-butyl 7-substituted derivativesBOUZARD, D; DI CESARE, P; FUNG-TOMC, J et al.Journal of medicinal chemistry (Print). 1990, Vol 33, Num 5, pp 1344-1352, issn 0022-2623, 9 p.Article

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