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Volumn 42, Issue 44, 2003, Pages 5465-5468

Biomimetic Total Synthesis of Litseaverticillols A, C, D, F, and G: Singlet-Oxygen-Initiated Cascades

Author keywords

Biomimetic synthesis; Ene reaction; Natural products; Singlet oxygen; Total synthesis

Indexed keywords

STEREOCHEMISTRY; SYNTHESIS (CHEMICAL); VIRUSES;

EID: 0344413533     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200352180     Document Type: Article
Times cited : (62)

References (30)
  • 4
    • 0037423972 scopus 로고    scopus 로고
    • For a review of cascade sequences employed in synthesis, as well as a discussion of examples of biomimetic variants that give racemic natural products from achiral precursors, see: K. C. Nicolaou, T. Montagnon, S. A. Snyder, Chem. Commun. 2003, 551-564.
    • (2003) Chem. Commun. , pp. 551-564
    • Nicolaou, K.C.1    Montagnon, T.2    Snyder, S.A.3
  • 25
    • 84985553269 scopus 로고
    • K. Gollnick, A. Griesbeck, Angew. Chem. 1983, 95, 751; Angew. Chem. Int. Ed. Engl. 1983, 22, 726-727.
    • (1983) Angew. Chem. Int. Ed. Engl. , vol.22 , pp. 726-727
  • 26
    • 0000580727 scopus 로고    scopus 로고
    • For a review about the regioselectivity and stereoselectivity of the singlet-oxygen-ene reaction, see: M. Prein, W. Adam, Angew. Chem. 1996, 108, 519-538; Angew. Chem. Int. Ed. Engl. 1996, 35, 477-494.
    • (1996) Angew. Chem. , vol.108 , pp. 519-538
    • Prein, M.1    Adam, W.2
  • 27
    • 33748241758 scopus 로고    scopus 로고
    • For a review about the regioselectivity and stereoselectivity of the singlet-oxygen-ene reaction, see: M. Prein, W. Adam, Angew. Chem. 1996, 108, 519-538; Angew. Chem. Int. Ed. Engl. 1996, 35, 477-494.
    • (1996) Angew. Chem. Int. Ed. Engl. , vol.35 , pp. 477-494


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.