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Volumn 2008, Issue 14, 2008, Pages 314-319

A second generation synthesis of the cruentaren A core structure based on oxetane and oxirane opening reactions

Author keywords

Aldol; Cruentaren A; Oxetane opening; Protecting group

Indexed keywords


EID: 58949090863     PISSN: 1551-7012     EISSN: 15517012     Source Type: Journal    
DOI: 10.3998/ark.5550190.0009.e29     Document Type: Article
Times cited : (6)

References (44)
  • 15
    • 0000775011 scopus 로고    scopus 로고
    • For some illustrative examples, see: a
    • For some illustrative examples, see: (a) A. Fürstner, G. Seidel, Angew. Chem. 1998, 110, 1758;
    • (1998) Angew. Chem , vol.110 , pp. 1758
    • Fürstner, A.1    Seidel, G.2
  • 16
    • 0038731101 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 1998, 37, 1734-1736;
    • (1998) Angew. Chem. Int. Ed , vol.37 , pp. 1734-1736
  • 22
    • 3543026290 scopus 로고    scopus 로고
    • This amine is commercially available but can also be prepared from the corresponding acid via Hofmann degradation: (a) Pickaert, G, Cesario, M, Ziessel, R. J. Org. Chem. 2004, 69, 5335;
    • This amine is commercially available but can also be prepared from the corresponding acid via Hofmann degradation: (a) Pickaert, G.; Cesario, M.; Ziessel, R. J. Org. Chem. 2004, 69, 5335;
  • 33
    • 2442512129 scopus 로고    scopus 로고
    • For other preparations, see
    • For other preparations, see: Smith, A. B., III; Fox, R. J. Org. Lett. 2004, 6, 1477.
    • (2004) Org. Lett , vol.6 , pp. 1477
    • Smith III, A.B.1    Fox, R.J.2
  • 34
    • 4444313912 scopus 로고    scopus 로고
    • For a related aldol reaction with the corresponding benzyloxy acetaldehyde, see
    • For a related aldol reaction with the corresponding benzyloxy acetaldehyde, see: Arai, N.; Chikaraishi, N.; Omura, S.; Kuwajima, I. Org. Lett. 2004, 6, 2845.
    • (2004) Org. Lett , vol.6 , pp. 2845
    • Arai, N.1    Chikaraishi, N.2    Omura, S.3    Kuwajima, I.4
  • 35
    • 25844435856 scopus 로고    scopus 로고
    • For a synthesis of a diastereomer of oxetane 27, see: Trost, B. M.; Wrobleski, S. T.; Chisholm, J. D.; Harrington, P. E.; Jung, M. J. Am. Chem. Soc. 2005, 127, 13589.
    • For a synthesis of a diastereomer of oxetane 27, see: Trost, B. M.; Wrobleski, S. T.; Chisholm, J. D.; Harrington, P. E.; Jung, M. J. Am. Chem. Soc. 2005, 127, 13589.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.