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Volumn 72, Issue 19, 2007, Pages 7135-7147

Pestalotiopsin A. Side chain installation and exhaustive probing of olefin metathesis as a possible tool for elaborating the cyclononene ring

Author keywords

[No Author keywords available]

Indexed keywords

DEXTROROTATORY CYCLOBUTANOL; PESTALOTIOPSIN A; RING-CLOSING METATHESIS;

EID: 34548707029     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo070862j     Document Type: Article
Times cited : (33)

References (63)
  • 24
    • 34548774593 scopus 로고    scopus 로고
    • Ph.D. Dissertation, The Ohio State University
    • Dong, S. Ph.D. Dissertation, The Ohio State University, 2007.
    • (2007)
    • Dong, S.1
  • 29
    • 0001654231 scopus 로고
    • and references therein
    • (b) Schroder, M. Chem. Rev. 1980, 80, 187 and references therein.
    • (1980) Chem. Rev , vol.80 , pp. 187
    • Schroder, M.1
  • 33
    • 34548728645 scopus 로고    scopus 로고
    • Pyridine was applied to avoid epoxidation of the resulting 2,2-disubstituted olefin. See: (a) Grieco, P. A.; Yokoyama, Y.; Gilman, S.; Nishizawa, M. J. Org. Chem. 1977, 42, 1977.
    • Pyridine was applied to avoid epoxidation of the resulting 2,2-disubstituted olefin. See: (a) Grieco, P. A.; Yokoyama, Y.; Gilman, S.; Nishizawa, M. J. Org. Chem. 1977, 42, 1977.
  • 50
    • 34548722794 scopus 로고    scopus 로고
    • US Patent No. US20070043180A1
    • Zhan, Z. J. US Patent No. US20070043180A1.
    • Zhan, Z.J.1
  • 53
    • 0035800494 scopus 로고    scopus 로고
    • The observation of isomerization products does not necessarily mean that the metathesis catalyst interacts directly with the alkene. Impurities in the metathesis catalyst Furstner, A, Ackermann, L, Gabor, B, Goddard, R, Lehmann, C. W, Mynott, R, Stelzer, F, Thiel, O. R. Chem. Eur. J. 2001, 7, 3236
    • The observation of isomerization products does not necessarily mean that the metathesis catalyst interacts directly with the alkene. Impurities in the metathesis catalyst (Furstner, A.; Ackermann, L.; Gabor, B.; Goddard, R.; Lehmann, C. W.; Mynott, R.; Stelzer, F.; Thiel, O. R. Chem. Eur. J. 2001, 7, 3236)
  • 54
    • 2942678732 scopus 로고    scopus 로고
    • or decomposition products thereof (Hong, S. H.; Day, M. W.; Grubbs, R. H. J. Am. Chem. Soc. 2004, 126, 7414)
    • or decomposition products thereof (Hong, S. H.; Day, M. W.; Grubbs, R. H. J. Am. Chem. Soc. 2004, 126, 7414)
  • 55
    • 29044439970 scopus 로고    scopus 로고
    • might be responsible. Attempts to suppress this side reaction with additives have been probed (Hong, S. H.; Sanders, D. P.; Lee, C. W.; Grubbs, R. H. J. Am. Chem. Soc. 2005, 127, 17160).
    • might be responsible. Attempts to suppress this side reaction with additives have been probed (Hong, S. H.; Sanders, D. P.; Lee, C. W.; Grubbs, R. H. J. Am. Chem. Soc. 2005, 127, 17160).
  • 63
    • 0023785118 scopus 로고
    • For an example of an alternative tactic as applied to a synthesis of punctaporonin
    • For an example of an alternative tactic as applied to a synthesis of punctaporonin B, consult: Kende, A. S.; Kaldor, I.; Aslanian, R. J. Am. Chem. Soc. 1988, 110, 6265.
    • (1988) J. Am. Chem. Soc , vol.110 , pp. 6265
    • consult, B.1    Kende, A.S.2    Kaldor, I.3    Aslanian, R.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.