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Volumn 124, Issue 46, 2002, Pages 13670-13671

Synthesis of leucascandrolide A via a spontaneous macrolactolization

Author keywords

[No Author keywords available]

Indexed keywords

LEUCASCANDROLIDE A; NATURAL PRODUCT; UNCLASSIFIED DRUG;

EID: 0037146080     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja028428g     Document Type: Article
Times cited : (95)

References (21)
  • 2
    • 0011738567 scopus 로고    scopus 로고
    • note
    • Subsequent samples of the sponge did not contain leucascandrolide A, strongly suggesting the microbial origin of this natural product.
  • 9
    • 0001767306 scopus 로고
    • For formation of 1.3-dioxanes via Lewis acid or Bronsted acid-catalyzed macrotransacetalization, see: Still, W. C.; Li, G. J. Am. Chem. Soc. 1993, 115, 3804. (b) Wender, P. A.; Brabander, J. D.; Harran, P. G.; Jimenez, J. M.; Koehler, M. F. T.; Lippa, B.; Park, C. M.; Shiozaki, M. J. Am. Chem. Soc. 1998, 120, 4534.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 3804
    • Still, W.C.1    Li, G.2
  • 11
    • 0027180369 scopus 로고
    • For cyanation of alkynyl zincs, see: Klement, I.; Lennick, K.; Tucker, C. E.; Knochel, P. Tetrahedron Lett. 1993, 34, 4623. For cyanation of lithium enolates, see: Kahne, D.; Collum, D. B. Tetrahedron Lett. 1981, 22, 5011.
    • (1993) Tetrahedron Lett. , vol.34 , pp. 4623
    • Klement, I.1    Lennick, K.2    Tucker, C.E.3    Knochel, P.4
  • 12
    • 0000814872 scopus 로고
    • For cyanation of alkynyl zincs, see: Klement, I.; Lennick, K.; Tucker, C. E.; Knochel, P. Tetrahedron Lett. 1993, 34, 4623. For cyanation of lithium enolates, see: Kahne, D.; Collum, D. B. Tetrahedron Lett. 1981, 22, 5011.
    • (1981) Tetrahedron Lett , vol.22 , pp. 5011
    • Kahne, D.1    Collum, D.B.2
  • 13
    • 18444417883 scopus 로고
    • and reference cited therein
    • (a) Doyle, M. P. Chem. Rev. 1986, 86, 919 and reference cited therein.
    • (1986) Chem. Rev. , vol.86 , pp. 919
    • Doyle, M.P.1
  • 16
    • 0011706538 scopus 로고    scopus 로고
    • For details, see the Supporting Information
    • For details, see the Supporting Information.
  • 17
    • 0011742376 scopus 로고    scopus 로고
    • note
    • 8
  • 18
    • 0011766181 scopus 로고    scopus 로고
    • note
    • 7.
  • 19
    • 0011765301 scopus 로고    scopus 로고
    • note
    • 17 epimeric triol 19 to the oxidative cleavage conditions resulted only in formation of the corresponding hydroxy aldehyde 20.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.