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Volumn , Issue 17, 2010, Pages 2654-2658

Efficient bis-C-aminoglycosylation toward the synthesis of the pluramycins

Author keywords

amino sugar; bis C glycoside; natural product synthesis; O C glycoside rearrangement; pluramycin type antibiotics

Indexed keywords

AMINE; AMINOGLYCOSIDE; ANGOLOSAMINE; PLURAMYCIN; UNCLASSIFIED DRUG; VANCOSAMINE;

EID: 77958029716     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0030-1258766     Document Type: Article
Times cited : (10)

References (38)
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    • Resorcylic ester 3 was synthesized as shown below (Scheme 9). For the preparation of the intermediate 24, see
    • Resorcylic ester 3 was synthesized as shown below (Scheme 9). For the preparation of the intermediate 24, see:, Hadfield A, Schweitzer H, Trova M P., Green K, Synth. Commun. 1994 24 1025
    • (1994) Synth. Commun. , vol.24 , pp. 1025
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  • 19
    • 33344474497 scopus 로고    scopus 로고
    • Vancosaminyl acetate 4 was synthesized as shown below (Scheme10). For the preparation of the intermediate 25, see
    • Vancosaminyl acetate 4 was synthesized as shown below (Scheme10). For the preparation of the intermediate 25, see:, Hsu D.-S, Matsumoto T, Suzuki K, Synlett 2006 469
    • (2006) Synlett , pp. 469
    • Hsu, D.-S.1    Matsumoto, T.2    Suzuki, K.3
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    • For a review on the Suzuki-Miyaura reaction, see
    • For a review on the Suzuki-Miyaura reaction, see:, Miyaura N, Suzuki A, Chem. Rev. 1995 95 2457
    • (1995) Chem. Rev. , vol.95 , pp. 2457
    • Miyaura, N.1    Suzuki, A.2
  • 35
    • 0026590352 scopus 로고
    • For the generation and cycloadditions of the benzynes containing C -glycoside moieties, see
    • For the generation and cycloadditions of the benzynes containing C -glycoside moieties, see:, Matsumoto T, Hosoya T, Suzuki K, J. Am. Chem. Soc. 1992 114 3568
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    • Matsumoto, T.1    Hosoya, T.2    Suzuki, K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.