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Volumn 63, Issue 21, 1998, Pages 7505-7515

Efficient conditions for conversion of 2-substituted furans into 4-oxygenated 2-enoic acids and its application to synthesis of (+)-aspicilin, (+)-patulolide a, and (-)-pyrenophorin

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EID: 0000510466     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo980942a     Document Type: Article
Times cited : (139)

References (94)
  • 17
    • 0013311854 scopus 로고
    • (e) Gunn, B. P. Heterocydes 1985, 23, 3061-3067
    • (1985) Heterocydes , vol.23 , pp. 3061-3067
    • Gunn, B.P.1
  • 25
    • 0000891348 scopus 로고
    • Trost, B. M.; Fleming, L; Pattenden, G., Eds.; Pergamon: New York
    • (b) Knight, D. W. In Comprehensive Organic Synthesis; Trost, B. M.; Fleming, L; Pattenden, G., Eds.; Pergamon: New York, 1991; Vol. 3, pp 481-520.
    • (1991) Comprehensive Organic Synthesis , vol.3 , pp. 481-520
    • Knight, D.W.1
  • 30
    • 85034199210 scopus 로고    scopus 로고
    • Although the method using 2-alkoxyfuran originally published by Takei is efficient, this approach suffers from inadequacy of a side chain-manipulation(s) due to instability of alkoxyfuran
    • Although the method using 2-alkoxyfuran originally published by Takei is efficient, this approach suffers from inadequacy of a side chain-manipulation(s) due to instability of alkoxyfuran:
  • 35
    • 85034168141 scopus 로고    scopus 로고
    • NBS has been used to convert furfuryl alcohols and related compounds into 2H-pyran-3(6H)-ones
    • NBS has been used to convert furfuryl alcohols and related compounds into 2H-pyran-3(6H)-ones:
  • 66
    • 85034172236 scopus 로고    scopus 로고
    • note
    • 4 solution in some cases.
  • 72
    • 0001005278 scopus 로고
    • Dauben, W. G., Ed.; Wiley: New York
    • Zweifel, G.; Miller, J. A. In Organic Reactions; Dauben, W. G., Ed.; Wiley: New York, 1984; Vol. 32, pp 375-517.
    • (1984) Organic Reactions , vol.32 , pp. 375-517
    • Zweifel, G.1    Miller, J.A.2
  • 73
    • 85034198176 scopus 로고    scopus 로고
    • Purchased from Merck.
    • Purchased from Merck.
  • 80
    • 85034177648 scopus 로고    scopus 로고
    • Formation of 30 is explained by considering the cation i where the abstraction of Hb by pyridine is competitive with the desired reaction (A) due to the steric hinderence by the MOM-oxy group.
    • Formation of 30 is explained by considering the cation i where the abstraction of Hb by pyridine is competitive with the desired reaction (A) due to the steric hinderence by the MOM-oxy group.
  • 93
    • 85034163396 scopus 로고    scopus 로고
    • Reaction was carried out by T. Okui of our laboratory.
    • Reaction was carried out by T. Okui of our laboratory.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.