Search Results - "ATARASHI, SHOHGO"

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  1. 1

    (Fluorocyclopropyl)quinolones. 2. Synthesis and Stereochemical Structure-Activity Relationships of Chiral 7-(7-Amino-5-azaspiro[2.4]heptan-5-yl)-1-(2-fluorocyclopropyl)quinolone Antibacterial Agents by Kimura, Youichi, Atarashi, Shohgo, Kawakami, Katsuhiro, Sato, Kenichi, Hayakawa, Isao

    Published in Journal of medicinal chemistry (01-09-1994)
    “…A series of novel chiral 7-(7-amino-5-azaspiro[2.4]heptan-4-yl)-8-chloro-1-(2-fluo rocyclopropyl)- quinolones were synthesized as a continuation of a research…”
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  2. 2

    Fluorocyclopropyl quinolones. 1. Synthesis and structure-activity relationships of 1-(2-fluorocyclopropyl)-3-pyridonecarboxylic acid antibacterial agents by Atarashi, Shohgo, Imamura, Masazumi, Kimura, Youichi, Yoshida, Atomi, Hayakawa, Isao

    Published in Journal of medicinal chemistry (01-10-1993)
    “…A series of 1-(2-fluorocyclopropyl)-3-pyridonecarboxylic acids has been prepared. These derivatives are characterized by having a fluorine atom at the…”
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    Journal Article
  3. 3

    Synthesis and Antibacterial Activity of Novel Pyridobenzoxazine Analogues by KAWAKAMI, Katsuhiro, ATARASHI, Shohgo, KIMURA, Youichi, TAKEUMURA, Makoto, HAYAKAWA, Isao

    Published in Chemical & pharmaceutical bulletin (01-11-1998)
    “…A series of novel LVFX (7) analogues bearing 4, 4-dialkyl-3-aminopyrrolidines at the C-10 position of pyridobenzoxazine was synthesized and their antibacterial…”
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  4. 4

    Synthesis and Antibacterial Activities of Optically Active Ofloxacin and Its Fluoromethyl Derivative by ATARASHI, SHOHGO, YOKOHAMA, SHUICHI, YAMAZAKI, KEN-ICHI, SAKANO, KATSU-ICHI, IMAMURA, MASAZUMI, HAYAKAWA, ISAO

    “…Two optically active (100% enantiomeric excess) isomers (13a and 13b) of ofloxacin (1) [(±) -ofloxacin; DL-8280; (±) -9-fluoro-2, 3-dihydro-3-methyl-10-…”
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    Regio- and Stereoselective Synthesis of Carbocyclic 2', 3'-Dideoxy-3'-fluoro Nucleosides as Potential Antiviral Agents by NAKAYAMA, Toshiaki, MATSUMURA, Yasushi, MORIZAWA, Yoshitomi, YASUDA, Arata, UCHIDA, Keiichi, TAKASE, Hiroyuki, MURAKAMI, Yoichi, ATARASHI, Shohgo, IKEUCHI, Tohru, OSADA, Yasuaki

    “…The synthesis and antiviral activity of racemic carbocyclic 2', 3'-dideoxy-3'-fluoro nucleosides are reported. Carbocyclic 2', 3'-dideoxy-3'-fluoro nucleosides…”
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  7. 7

    Bicyclo [3. 3. 1] nonanes as Synthetic Intermediates. V. The Baeyer-Villiger Oxidation of Bicyclo [3. 3. 1] nonane-3, 7-dione and Its Congeners by MOMOSE, TAKEFUMI, ATARASHI, SHOHGO

    “…The Baeyer-Villiger oxidation, which is known to be unsuccessful with the bicyclo [3. 3. 1] nonan-3-one system, was shown to proceed smoothyl with the 3,…”
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  8. 8

    Modification of the cysteamine side chain of thienamycin. II by Sato, M, Takemura, M, Atarashi, S, Higashi, K, Fujiwara, H, Nagahara, T, Furukawa, M, Ikeuchi, T, Ozawa, S, Nishizawa, N

    Published in Journal of antibiotics (1987)
    “…A new type of thienamycin derivatives (3a-3j, 4a, 4b), having a monothioacetal or a thioacetal side chain at the C-2 position was prepared, and the…”
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  9. 9

    Modification of the cysteamine side chain of thienamycin. III by Sato, M, Takemura, M, Atarashi, S, Higashi, K, Nagahara, T, Furukawa, M, Ikeuchi, T, Osada, Y

    Published in Journal of antibiotics (01-01-1987)
    “…Thienamycin derivatives (4) having a cyclic amidine moiety at the C-2 position were prepared. The susceptibility to renal dehydropeptidase-1 and the…”
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  10. 10

    Bicyclo [3. 3. 1]nonanes as Synthetic Intermediates. IV. Behavior of Bicyclo [3. n. 1] alkan-3-ones toward the Baeyer-Villiger Oxidation by MOMOSE, TAKEFUMI, MURAOKA, OSAMU, ATARASHI, SHOHGO, HORITA, TAMIKO

    Published in Chemical & pharmaceutical bulletin (01-01-1979)
    “…The Baeyer-Villiger oxidation of bicyclo [3. n. 1] alkan-3-ones and related systems is described. Bicyclo [3. 3. 1] nonan-2-one (8) was oxidized into the…”
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  11. 11

    Asymmetric reduction of 7,8-difluoro-3-methyl-2H-1,4-benzoxazine. Synthesis of a key intermediate of (S)-(-)-ofloxacin (DR-3355) by Atarashi, Shohgo, Tsurumi, Hideaki, Fujiwara, Toshihiro, Hayakawa, Isao

    Published in Journal of heterocyclic chemistry (01-02-1991)
    “…An efficient, highly enantioselective synthesis of (S)‐(‐)‐7,8‐difluoro‐2,3‐dihydro‐3‐methyl‐4H‐1,4‐benzoxazine, a key intermediate of (S)‐(‐)‐ofloxacin, using…”
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  12. 12

    Synthesis and Structure-Activity Relationships of 7-[3-(1-Aminoalkyl)pyrrolidinyl]-and 7-[3-1-aminocycloalkyl)pyrrolidinyl]-quinolone Antibacterials by KIMURA, Youichi, ATARASHI, Shohgo, TAKAHASHI, Masanobu, HAYAKAWA, Isao

    Published in Chemical & pharmaceutical bulletin (15-07-1994)
    “…A series of 7-[3-(1-aminoalkyl and 1-aminocycloalkyl)-1-pyrrolidinyl]quinolones have been prepared and their biological properties evaluated. Among them,…”
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  13. 13

    Asymmetric reduction of 7,8‐difluoro‐3‐methyl‐2 H ‐1,4‐benzoxazine. Synthesis of a key intermediate of ( S )‐(‐)‐ofloxacin (DR‐3355) by Atarashi, Shohgo, Tsurumi, Hideaki, Fujiwara, Toshihiro, Hayakawa, Isao

    Published in Journal of heterocyclic chemistry (01-02-1991)
    “…An efficient, highly enantioselective synthesis of ( S )‐(‐)‐7,8‐difluoro‐2,3‐dihydro‐3‐methyl‐4 H ‐1,4‐benzoxazine, a key intermediate of ( S )‐(‐)‐ofloxacin,…”
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