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Volumn 10, Issue 39, 2012, Pages 7884-7899

Total synthesis of the marine toxin phorboxazole A using palladium(ii)-mediated intramolecular alkoxycarbonylation for tetrahydropyran synthesis

Author keywords

[No Author keywords available]

Indexed keywords

ALKOXYCARBONYLATION; ANTI-TUMOR AGENTS; CATALYZED COUPLING; LINEAR SEQUENCE; STEREO-SELECTIVE; TERMINAL ALKYNE; TETRAHYDROPYRAN; TOTAL SYNTHESIS;

EID: 84874957077     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c2ob25766a     Document Type: Article
Times cited : (16)

References (86)
  • 69
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    • P6388j
    • Chem. Abstr., 1976, 85, P6388j
    • (1976) Chem. Abstr. , vol.85
  • 70
    • 0141665446 scopus 로고    scopus 로고
    • ed. I. Fleming, Thieme, Stuttgart, Germany
    • J. D. White and R. G. Carter, Science of Synthesis, ed., I. Fleming, Thieme, Stuttgart, Germany, 2002, vol. 4, pp. 371-412
    • (2002) Science of Synthesis , vol.4 , pp. 371-412
    • White, J.D.1    Carter, R.G.2
  • 77
    • 2142858450 scopus 로고
    • Evans' synthesis of phorboxazole B 5a avoided this problem by masking the C7 exo methylene function as an alcohol A deuterium exchange experiment revealed that deprotonation can occur at the open C30 position of oxazole 80 under conditions that deprotonate C32
    • I. Ohtani T. Kusumi Y. Kashman H. Kakisawa J. Am. Chem. Soc. 1991 113 4092
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 4092
    • Ohtani, I.1    Kusumi, T.2    Kashman, Y.3    Kakisawa, H.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.