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Volumn 118, Issue 36, 1996, Pages 8757-8758

Biosynthesis of DTX-4: Confirmation of a polyketide pathway, proof of a Baeyer - Villiger oxidation step, and evidence for an unusual carbon deletion process

Author keywords

[No Author keywords available]

Indexed keywords

DTX 4; TOXIN; UNCLASSIFIED DRUG;

EID: 0001540497     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja961715y     Document Type: Article
Times cited : (92)

References (32)
  • 17
    • 0000537752 scopus 로고
    • and references therein
    • Simpson, T. J. Chem. Ind. 1995, 407-411 and references therein.
    • (1995) Chem. Ind. , pp. 407-411
    • Simpson, T.J.1
  • 18
    • 10144257102 scopus 로고    scopus 로고
    • note
    • 13C enrichment of 2.
  • 19
    • 10144222816 scopus 로고    scopus 로고
    • note
    • 1H, D}-broadband decoupling, suppression of NOE for 5 s between acquisition periods (1 s). Details of the calculation of isotope enrichment at labeled positions are described in the supporting information.
  • 20
    • 10144221248 scopus 로고    scopus 로고
    • note
    • 13C was 3.9%, 3.9%, and 3.7% (SD ca. ± 0.6%) in the first experiment; 7.8%, 7.6%, and 7.3% (SD ca. ±0.8%) in the second.
  • 30
    • 10144234727 scopus 로고    scopus 로고
    • note
    • Other Favorski-type mechanisms can be envisaged invoking a 3-halo or 3,4 epoxide intermediate of a β diketone that would yield an olefinic or hydroxy ketide, respectively.
  • 32
    • 10144234053 scopus 로고    scopus 로고
    • note
    • 18c


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.