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Volumn 49, Issue 50, 2008, Pages 7197-7199

Synthetic studies on dragmacidin D: synthesis of the left-hand fragment

Author keywords

[No Author keywords available]

Indexed keywords

DRAGMACIDIN D; INDOLE ALKALOID; NATURAL PRODUCT; NITRIC OXIDE SYNTHASE; PHOSPHOPROTEIN PHOSPHATASE; UNCLASSIFIED DRUG;

EID: 54449095064     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2008.10.020     Document Type: Article
Times cited : (13)

References (24)
  • 7
    • 54449086947 scopus 로고    scopus 로고
    • Longley, R. E.; Isbrucker, R. A.; Wright, A. E. U.S. Patent, 6,087,363, 2000.
    • Longley, R. E.; Isbrucker, R. A.; Wright, A. E. U.S. Patent, 6,087,363, 2000.
  • 11
    • 33750464876 scopus 로고    scopus 로고
    • For diverted total synthesis of natural products, see:
    • For diverted total synthesis of natural products, see:. Wilson R.M., and Danishefsky S.J. J. Org. Chem. 71 (2006) 8329-8351
    • (2006) J. Org. Chem. , vol.71 , pp. 8329-8351
    • Wilson, R.M.1    Danishefsky, S.J.2
  • 12
    • 51349111666 scopus 로고    scopus 로고
    • For a recent review, see:
    • For a recent review, see:. Doucet H. Eur. J. Org. Chem. (2008) 2013-2030
    • (2008) Eur. J. Org. Chem. , pp. 2013-2030
    • Doucet, H.1
  • 13
    • 0000159355 scopus 로고    scopus 로고
    • Suzuki-Miyaura reaction of a related imidazolyl boronic acid has been reported to be unsuccessful in the synthesis of topsentin, see:
    • Suzuki-Miyaura reaction of a related imidazolyl boronic acid has been reported to be unsuccessful in the synthesis of topsentin, see:. Kawasaki I., Katsuma H., Nakayama Y., Yamashita M., and Ohta S. Heterocycles 48 (1998) 1887-1901
    • (1998) Heterocycles , vol.48 , pp. 1887-1901
    • Kawasaki, I.1    Katsuma, H.2    Nakayama, Y.3    Yamashita, M.4    Ohta, S.5
  • 20
    • 33947727055 scopus 로고    scopus 로고
    • For a recent review, see:
    • For a recent review, see:. Chinchilla R., and Najera C. Chem. Rev. 107 (2007) 874-922
    • (2007) Chem. Rev. , vol.107 , pp. 874-922
    • Chinchilla, R.1    Najera, C.2
  • 22
    • 54449100609 scopus 로고    scopus 로고
    • note
    • The synthesis of 13 will be published in a full account of this work.
  • 24
    • 54449094398 scopus 로고    scopus 로고
    • note
    • 1H NMR spectrum, since the coupling product 15 was contaminated with small quantities of reactants, which could not be completely removed by chromatographic purification.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.