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Volumn 38, Issue 3, 1985, Pages 346-371

Chemical modification of sulfazecin synthesis of 4-(substituted methyl)-2-azetidinone-l-sulfonic acid derivatives

Author keywords

[No Author keywords available]

Indexed keywords

4 METHYL 2 OXO 1 AZETIDINESULFONIC ACID DERIVATIVE; ANTIINFECTIVE AGENT; AZTREONAM; CARUMONAM; NEW DRUG; SULFAZECIN; UNCLASSIFIED DRUG;

EID: 0021959970     PISSN: 00218820     EISSN: 18811469     Source Type: Journal    
DOI: 10.7164/antibiotics.38.346     Document Type: Article
Times cited : (49)

References (13)
  • 2
    • 0021129015 scopus 로고
    • Chemical modification of sulfazecin. Synthesis of 4-methoxycarbonyl-2-azetidinone-l-sulfonic acid derivatives
    • Kishimoto, S.; M. Sendai, M. Tomimoto, S. Hashiguchi, T. Matsuo & M. Ochiai: Chemical modification of sulfazecin. Synthesis of 4-methoxycarbonyl-2-azetidinone-l-sulfonic acid derivatives. Chem. Pharm. Bull. 32: 2646-2659, 1984
    • (1984) Chem. Pharm. Bull. , vol.32 , pp. 2646-2659
    • Kishimoto, S.1    Sendai, M.2    Tomimoto, M.3    Hashiguchi, S.4    Matsuo, T.5    Ochiai, M.6
  • 3
    • 0017410318 scopus 로고
    • Nuclear analogues of β-Iactam antibiotics. 1. The total synthesis of a 7-oxo-1,3-diazabicyclo[3.2.0]heptane-2-carboxylic acid via a versatile monocyclic β-lactam intermediate
    • Huffman, W. F.; K. G. Holden, T. F. Buckley, III, J. G. Gleason & L. Wu: Nuclear analogues of β-Iactam antibiotics. 1. The total synthesis of a 7-oxo-1,3-diazabicyclo[3.2.0]heptane-2-carboxylic acid via a versatile monocyclic β-lactam intermediate. J. Am. Chem. Soc. 99: 2352-2353, 1977
    • (1977) J. Am. Chem. Soc. , vol.99 , pp. 2352-2353
    • Huffman, W.F.1    Holden, K.G.2    Buckley, T.F.3    Gleason, J.G.4    Wu, L.5
  • 4
    • 33947090431 scopus 로고
    • Stereospecific and stereoselective reactions. 1. Preparation of amines from alcohols
    • Mitsunobu, O.; M. Wada & T. Sano: Stereospecific and stereoselective reactions. 1. Preparation of amines from alcohols. J. Am. Chem. Soc. 94: 679-680, 1979
    • (1979) J. Am. Chem. Soc. , vol.94 , pp. 679-680
    • Mitsunobu, O.1    Wada, M.2    Sano, T.3
  • 5
    • 0019521918 scopus 로고
    • Synthesis and structure-activity relationships of 7β-[2-(2-aminothiazol-4-yl)acetamido]cephalosporin derivatives. V. Synthesis and antibacterial activity of 7β-[2-(2-aminothiazol-4-yl)-2-methoxyiminoacetamido]cephalos-porin derivatives and related compounds
    • Ochiai, M.; A. Morimoto, T. Miyawaki, Y. Matsushita, T. Okada, H. Natsugari & M. Kida: Synthesis and structure-activity relationships of 7β-[2-(2-aminothiazol-4-yl)acetamido]cephalosporin derivatives. V. Synthesis and antibacterial activity of 7β-[2-(2-aminothiazol-4-yl)-2-methoxyiminoacetamido]cephalos-porin derivatives and related compounds. J. Antibiotics 34: 171-185, 1981
    • (1981) J. Antibiotics , vol.34 , pp. 171-185
    • Ochiai, M.1    Morimoto, A.2    Miyawaki, T.3    Matsushita, Y.4    Okada, T.5    Natsugari, H.6    Kida, M.7
  • 6
    • 0012388367 scopus 로고
    • Monobactams. The conversion of 6-APA to (S)-3-amino-2-oxoazetidine-l-sulfonic acid and its 3 (RS)methyl derivative
    • Cimarusti, C. M.; H. E. Applegate, H. W. Chang, D. M. Floyd, W. H. Koster, W. A. Slusarchyk & M. G. Young: Monobactams. The conversion of 6-APA to (S)-3-amino-2-oxoazetidine-l-sulfonic acid and its 3 (RS)methyl derivative. J. Org. Chem. 47: 179-180, 1982
    • (1982) J. Org. Chem. , vol.47 , pp. 179-180
    • Cimarusti, C.M.1    Applegate, H.E.2    Chang, H.W.3    Floyd, D.M.4    Koster, W.H.5    Slusarchyk, W.A.6    Young, M.G.7
  • 7
    • 0020601227 scopus 로고
    • Synthesis and antibacterial activity of 3-acylamino-2-azetidinone-l-sulfonic acid derivatives
    • Matsuo, T.; T. Sugawara, H. Masuya, Y. Kawano, N. Noguchi & M. Ochiai: Synthesis and antibacterial activity of 3-acylamino-2-azetidinone-l-sulfonic acid derivatives. Chem. Pharm. Bull. 31: 1874-1884, 1983
    • (1983) Chem. Pharm. Bull. , vol.31 , pp. 1874-1884
    • Matsuo, T.1    Sugawara, T.2    Masuya, H.3    Kawano, Y.4    Noguchi, N.5    Ochiai, M.6
  • 8
    • 0021266177 scopus 로고
    • Synthesis of 3-acylamino-4-hydroxymethyl-2-oxo-l-sulfoazetidines and related compounds
    • Shibuya, M.; Y. Jinbo & S. Kubota: Synthesis of 3-acylamino-4-hydroxymethyl-2-oxo-l-sulfoazetidines and related compounds. Chem. Pharm. Bull. 32: 1303-1312, 1984
    • (1984) Chem. Pharm. Bull. , vol.32 , pp. 1303-1312
    • Shibuya, M.1    Jinbo, Y.2    Kubota, S.3
  • 10
    • 0020077544 scopus 로고
    • Azthreonam (SQ 26,776), a synthetic monobactam specifically active against aerobic Gram-negative bacteria
    • Sykes, R. B.; D. P. Bonner, K. Bush & N. H. Georgopapadakou: Azthreonam (SQ 26,776), a synthetic monobactam specifically active against aerobic Gram-negative bacteria. Antimicrob. Agents Chemother. 21: 85-92, 1982
    • (1982) Antimicrob. Agents Chemother. , vol.21 , pp. 85-92
    • Sykes, R.B.1    Bonner, D.P.2    Bush, K.3    Georgopapadakou, N.H.4
  • 12
    • 85004484069 scopus 로고
    • β-Lactamase stability and in vitro activity of AMA-1080 (Ro 17-2301). 23rd Intersci
    • Abstract 325 Las Vegas
    • Okonogi, K. & M. Kuno: β-Lactamase stability and in vitro activity of AMA-1080 (Ro 17-2301). 23rd Intersci. Conf. Antimicrob. Agents Chemother., Abstract No. 325. Las Vegas, 1983
    • (1983) Conf. Antimicrob. Agents Chemother.
    • Okonogi, K.1    Kuno, M.2
  • 13
    • 0019932198 scopus 로고
    • Oxidative Ar-dearylation of 2-azetidinones. p-Anisi-dine as a source of azetidinone nitrogen
    • Kronenthal, D. R.; C. Y. Han & M. K. Taylor: Oxidative Ar-dearylation of 2-azetidinones. p-Anisi-dine as a source of azetidinone nitrogen. J. Org. Chem. 47: 2765-2768, 1982
    • (1982) J. Org. Chem. , vol.47 , pp. 2765-2768
    • Kronenthal, D.R.1    Han, C.Y.2    Taylor, M.K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.