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Volumn 15, Issue 20, 2013, Pages 5306-5309

Transannular Diels-Alder/1,3-dipolar cycloaddition cascade of 1,3,4-oxadiazoles: Total synthesis of a unique set of vinblastine analogues

Author keywords

[No Author keywords available]

Indexed keywords

1,3,4-OXADIAZOLE; OXADIAZOLE; OXADIAZOLE DERIVATIVE; VINBLASTINE;

EID: 84886305653     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol402549n     Document Type: Article
Times cited : (39)

References (49)
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    • Neuss, N.; Neuss, M. N. In The Alkaloids; Brossi, A., Suffness, M., Eds.; Academic: San Diego, 1990; Vol. 37, p 229.
    • (1990) The Alkaloids , vol.37 , pp. 229
    • Neuss, N.1    Neuss, M.N.2
  • 6
    • 77957080344 scopus 로고
    • In; Brossi, A. Suffness, M. Academic: San Diego, Vol.
    • Pearce, H. L. In The Alkaloids; Brossi, A.; Suffness, M., Eds.; Academic: San Diego, 1990; Vol. 37, p 145.
    • (1990) The Alkaloids , vol.37 , pp. 145
    • Pearce, H.L.1
  • 8
    • 84885457038 scopus 로고    scopus 로고
    • ACS Med. Chem. Lett. 2013, 4, in press (DOI: 10.1021/ml400281w).
    • Barker, T. J.; Duncan, K. K.; Otrubova, K.; Boger, D. L. ACS Med. Chem. Lett. 2013, 4, in press (DOI: 10.1021/ml400281w).
    • Barker, T.J.1    Duncan, K.K.2    Otrubova, K.3    Boger, D.L.4
  • 20
    • 77957095647 scopus 로고
    • In; Brossi, A. Suffness, M. Academic: San Diego, Vol.
    • Kuehne, M. E.; Marko, I. In The Alkaloids; Brossi, A.; Suffness, M., Eds.; Academic: San Diego, 1990; Vol. 37, p 77.
    • (1990) The Alkaloids , vol.37 , pp. 77
    • Kuehne, M.E.1    Marko, I.2
  • 44
    • 84886269159 scopus 로고    scopus 로고
    • The structure and relative stereochemistry of 15 were confirmed by X-ray (CCDC 956386).
    • The structure and relative stereochemistry of 15 were confirmed by X-ray (CCDC 956386).
  • 45
    • 84886272013 scopus 로고    scopus 로고
    • The structure and absolute stereochemistry of 22 (unnatural enantiomer) were established by X-ray (CCDC 956388).
    • The structure and absolute stereochemistry of 22 (unnatural enantiomer) were established by X-ray (CCDC 956388).
  • 46
    • 84886267762 scopus 로고    scopus 로고
    • The structure and absolute stereochemistry of 23 (natural enantiomer) were established by X-ray (CCDC 956389).
    • The structure and absolute stereochemistry of 23 (natural enantiomer) were established by X-ray (CCDC 956389).
  • 47
    • 84886269156 scopus 로고    scopus 로고
    • The structure and absolute stereochemistry of 25 (unnatural enantiomer) were established by X-ray (CCDC 956387).
    • The structure and absolute stereochemistry of 25 (unnatural enantiomer) were established by X-ray (CCDC 956387).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.