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Volumn 40, Issue 22, 1999, Pages 4145-4148

The enantioselective total synthesis of the antitumor macrolide natural product rhizoxin D

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE; ANTINEOPLASTIC AGENT; MACROLIDE; NATURAL PRODUCT; RHIZOXIN; RHIZOXIN D; UNCLASSIFIED DRUG;

EID: 0033612278     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)00731-5     Document Type: Article
Times cited : (34)

References (33)
  • 3
    • 0031460435 scopus 로고    scopus 로고
    • and references cited. The palmitate ester of rhizoxin (RS-1541) has also been studied
    • See, for example, Onozawa, C.; Shimamura, M.; Iwasaki, S.; Oikawa, T. Jpn. J. Cancer Res. 1997, 88, 1125 and references cited. The palmitate ester of rhizoxin (RS-1541) has also been studied ( see, for example Kurihara, A.; Shibayama, Y.; Kasuya, A.; Ikeda, M.; Hisaoka, M. J. Drug Target. 1998, 5, 491).
    • (1997) Jpn. J. Cancer Res. , vol.88 , pp. 1125
    • Onozawa, C.1    Shimamura, M.2    Iwasaki, S.3    Oikawa, T.4
  • 4
    • 0031796843 scopus 로고    scopus 로고
    • See, for example, Onozawa, C.; Shimamura, M.; Iwasaki, S.; Oikawa, T. Jpn. J. Cancer Res. 1997, 88, 1125 and references cited. The palmitate ester of rhizoxin (RS-1541) has also been studied ( see, for example Kurihara, A.; Shibayama, Y.; Kasuya, A.; Ikeda, M.; Hisaoka, M. J. Drug Target. 1998, 5, 491).
    • (1998) J. Drug Target. , vol.5 , pp. 491
    • Kurihara, A.1    Shibayama, Y.2    Kasuya, A.3    Ikeda, M.4    Hisaoka, M.5
  • 19
    • 0029113710 scopus 로고
    • For our initial efforts in this area, see: (a) Lafontaine, J. A.; Leahy, J. W. Tetrahedron Lett. 1995, 36, 6029. (b) Provencal, D. P.; Gardelli, C.; Lafontaine, J. A.; Leahy, J. W. Tetrahedron Lett. 1995, 36, 6033.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 6029
    • Lafontaine, J.A.1    Leahy, J.W.2
  • 21
    • 0013572131 scopus 로고    scopus 로고
    • unpublished results
    • Lafontaine, J. A., unpublished results.
    • Lafontaine, J.A.1
  • 22
    • 0013597606 scopus 로고    scopus 로고
    • note
    • 10 in the following manner: (equation presented)
  • 24
    • 0002005554 scopus 로고
    • For an example of the use of barium hydroxide in Horner-Emmons olefinations, see: Paterson, I.; Yeung, K.; Smaill, J. B. Synlett 1993, 774.
    • (1993) Synlett , pp. 774
    • Paterson, I.1    Yeung, K.2    Smaill, J.B.3
  • 27
    • 0013622279 scopus 로고    scopus 로고
    • note
    • 8Si: C, 66.07; H, 7.96; N, 3.95. Found: C, 65.74; H, 8.33; N, 3.67.
  • 29
    • 0013569699 scopus 로고    scopus 로고
    • note
    • 2: C, 56.73; H, 8.37; N, 2.28. Found: C, 56.80; H, 8.32; N, 2.13.
  • 30
    • 0013622992 scopus 로고    scopus 로고
    • note
    • +): 1106.6842. Found: 1106.6849.
  • 33
    • 0013598988 scopus 로고    scopus 로고
    • note
    • 3. Elemental analytical data were obtained from MHW Laboratories, Phoenix, AZ. High resolution mass spectra were obtained from the University of California College of Chemistry Microanalytical Facility.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.