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Volumn 48, Issue 14, 2007, Pages 2607-2610

Total synthesis of (-)-martinellic acid

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOID; ALKENE; AZOMETHINE YLIDE; BRADYKININ; LACTAM; MARTINELLIC ACID; NATURAL PRODUCT; PYROGLUTAMIC ACID; PYRROLO[3,2 C]QUINOLINE; UNCLASSIFIED DRUG;

EID: 33847673690     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2007.02.008     Document Type: Article
Times cited : (40)

References (60)
  • 35
    • 33645761708 scopus 로고    scopus 로고
    • Professor Naito has informed us that his group has completed an asymmetric total synthesis of 2
    • Miyata O., Shirai A., Yoshino S., Takeda Y., Sugiura M., and Naito T. Synlett (2006) 893 Professor Naito has informed us that his group has completed an asymmetric total synthesis of 2
    • (2006) Synlett , pp. 893
    • Miyata, O.1    Shirai, A.2    Yoshino, S.3    Takeda, Y.4    Sugiura, M.5    Naito, T.6
  • 38
    • 33847665595 scopus 로고    scopus 로고
    • note
    • 7d,e. For similar strategies for introduction of the C2 side-chain see Refs. 17 and 18.
  • 41
    • 33847687724 scopus 로고    scopus 로고
    • note
    • 2O, 0%.
  • 48
    • 0026695725 scopus 로고
    • We are grateful to Professor Lhommet for providing experimental details
    • Fleurant A., Celerier J.P., and Lhommet G. Tetrahedron: Asymmetry 3 (1992) 695 We are grateful to Professor Lhommet for providing experimental details
    • (1992) Tetrahedron: Asymmetry , vol.3 , pp. 695
    • Fleurant, A.1    Celerier, J.P.2    Lhommet, G.3
  • 53
    • 33847651788 scopus 로고    scopus 로고
    • note
    • 2O: C, 56.77; H, 4.76; N, 6.30. Found: C, 56.60; H, 4.80; N, 6.42.
  • 54
    • 33847629997 scopus 로고    scopus 로고
    • note
    • 33 wherein non-equivalence of several signals was observed. On the other hand, when (-)-17 and (-)-18 were employed under otherwise identical conditions, only single absorptions were observed for the same signals. These experiments unequivocally demonstrate that both the cycloaddition precursors and adducts are single enantiomers, and by extrapolation so are subsequent intermediates.
  • 55
    • 33847626641 scopus 로고    scopus 로고
    • note
    • 12c.
  • 56
    • 33847641001 scopus 로고    scopus 로고
    • note
    • +). Found: 710.4609.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.