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Volumn 13, Issue 20, 2011, Pages 5524-5527

Structural revision and total synthesis of caraphenol B and C

Author keywords

[No Author keywords available]

Indexed keywords

CARAPHENOL B; CARAPHENOL C; PHENOL DERIVATIVE; RESVERATROL; STILBENE DERIVATIVE;

EID: 80054679077     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol2022406     Document Type: Article
Times cited : (43)

References (39)
  • 2
    • 79955014363 scopus 로고    scopus 로고
    • For a review on oligomeric natural products, see
    • For a review on oligomeric natural products, see: Snyder, S. A.; ElSohly, A. M.; Kontes, F. Nat. Prod. Rep. 2011, 28, 897-924
    • (2011) Nat. Prod. Rep. , vol.28 , pp. 897-924
    • Snyder, S.A.1    Elsohly, A.M.2    Kontes, F.3
  • 3
    • 85083347784 scopus 로고    scopus 로고
    • For a review on resveratrol synthetic work, see: In; Poupon, E. Nay, B. Wiley-VCH: Weinheim
    • For a review on resveratrol synthetic work, see: Snyder, S. A. In Biomimetic Organic Synthesis; Poupon, E.,; Nay, B., Eds.; Wiley-VCH: Weinheim, 2011; pp 695-721.
    • (2011) Biomimetic Organic Synthesis , pp. 695-721
    • Snyder, S.A.1
  • 22
    • 3943071801 scopus 로고    scopus 로고
    • Biological explorations are extensive. For recent work, see: and references therein
    • Biological explorations are extensive. For recent work, see: Wood, J. G.; Rogina, B.; Lavu, S.; Howitz, K.; Helfand, S. L.; Tatar, M.; Sinclair, D. Nature 2004, 430, 686-689 and references therein
    • (2004) Nature , vol.430 , pp. 686-689
    • Wood, J.G.1    Rogina, B.2    Lavu, S.3    Howitz, K.4    Helfand, S.L.5    Tatar, M.6    Sinclair, D.7
  • 29
  • 30
    • 0035795044 scopus 로고    scopus 로고
    • There is one other cis -disposed indane ring that we have identified, but it is directly attached to an eight-membered ring and thus is unique in that it is not an isolated system
    • There is one other cis -disposed indane ring that we have identified, but it is directly attached to an eight-membered ring and thus is unique in that it is not an isolated system: Yan, K.-X.; Terashima, K.; Takaya, Y.; Niwa, M. Tetrahedron 2001, 57, 2711-2715
    • (2001) Tetrahedron , vol.57 , pp. 2711-2715
    • Yan, K.-X.1    Terashima, K.2    Takaya, Y.3    Niwa, M.4
  • 37
    • 46249122373 scopus 로고    scopus 로고
    • 3N was also valuable in a hydrogenation, see
    • 3N was also valuable in a hydrogenation, see: Coquerel, Y.; Rodriguez, J. Arkivoc 2008, 227-237
    • (2008) Arkivoc , pp. 227-237
    • Coquerel, Y.1    Rodriguez, J.2
  • 38
    • 80054683303 scopus 로고    scopus 로고
    • Some of these opening steps were also performed in the following account: Chinese Patent Application CN 1634826 A 20050706.
    • Some of these opening steps were also performed in the following account: Sun, X.; Lin, G.; Hu, C.; Dong, J. Chinese Patent Application CN 1634826 A 20050706.
    • Sun, X.1    Lin, G.2    Hu, C.3    Dong, J.4
  • 39
    • 0242468048 scopus 로고    scopus 로고
    • In fact, the cores of the revised caraphenols can be found in higher-order structures where additional resveratrol units are attached
    • In fact, the cores of the revised caraphenols can be found in higher-order structures where additional resveratrol units are attached: Yang, G. X.; Hu, C. Q. Chin. Chem. Lett. 2003, 14, 1048-1050
    • (2003) Chin. Chem. Lett. , vol.14 , pp. 1048-1050
    • Yang, G.X.1    Hu, C.Q.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.