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Volumn 50, Issue 47, 1994, Pages 13347-13368

Absolute configuration of main chain of AAL-toxins.

Author keywords

AAL toxin; absolute configuration; Alternaria alternata

Indexed keywords

MYCOTOXIN;

EID: 0027973655     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(01)89343-1     Document Type: Article
Times cited : (29)

References (32)
  • 19
    • 84913985039 scopus 로고    scopus 로고
    • The results described here were presented at Second Tottori Internatinal Symposium on Host-Specific Toxin: Biosynthesis, Receptor and Molecular Biology in Tottori, Japan, on September 5, 1993.
  • 26
    • 84913985038 scopus 로고    scopus 로고
    • For non protected epoxide O-deacetyl-35, the epoxide opening was attempted under acidic and basic conditions. In both cases, unidentified by-products were predominated. Since the epoxidation of O-acetyl- 34 gave nearly 1:1 diastereomer mixture, predominant formation of 2,4-syn-diol 36b could be explained by acyl group assisted epoxide opening.
  • 27
    • 84913985037 scopus 로고    scopus 로고
    • iPrOH, 70% overall).
  • 28
    • 84913985036 scopus 로고    scopus 로고
    • 4, ether; iii. TsCl, DMAP, Py; iv. NaI, acetone, 71% overall).
  • 29
    • 84913985035 scopus 로고    scopus 로고
    • The numbering of all synthetic acetonides corresponds to those of AAL-toxins.
  • 31
    • 84913985034 scopus 로고    scopus 로고
    • 2c


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.