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Volumn 52, Issue 20, 2013, Pages 5382-5385

Synthesis of epoxyisoprostanes: Effects in reducing secretion of pro-inflammatory cytokines IL-6 and IL-12

Author keywords

anti inflammatory agents; C H insertion; isoprostanoids; natural products; oxidized phospholipids

Indexed keywords

ANTI-INFLAMMATORY AGENTS; C-H INSERTION; ISOPROSTANOIDS; NATURAL PRODUCTS; OXIDIZED PHOSPHOLIPIDS;

EID: 84877275641     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201300739     Document Type: Article
Times cited : (54)

References (53)
  • 2
    • 58449126169 scopus 로고    scopus 로고
    • for a comprehensive review on oxidized phospholipids, see:, U. Jahn, J.-M. Galano, T. Durand, Angew. Chem. 2008, 120, 5978-6041
    • (2008) Angew. Chem. , vol.120 , pp. 5978-6041
    • Jahn, U.1    Galano, J.-M.2    Durand, T.3
  • 3
    • 51449093769 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 5894-5955
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 5894-5955
  • 10
    • 2542460047 scopus 로고    scopus 로고
    • M. Navab, et al., J. Lipid Res. 2004, 45, 993-1007
    • (2004) J. Lipid Res. , vol.45 , pp. 993-1007
    • Navab, M.1
  • 18
    • 59049083939 scopus 로고    scopus 로고
    • Besides human-derived oxidized phospholipids our group is also interested in oxidized lipids from marine sources and their effect on humans; see
    • Besides human-derived oxidized phospholipids our group is also interested in oxidized lipids from marine sources and their effect on humans; see:, C. Nilewski, R. W. Geisser, E. M. Carreira, Nature 2009, 457, 573-576
    • (2009) Nature , vol.457 , pp. 573-576
    • Nilewski, C.1    Geisser, R.W.2    Carreira, E.M.3
  • 21
    • 80051762471 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2011, 50, 7940-7943
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 7940-7943
  • 27
    • 20444395864 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 3481-3484
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 3481-3484
  • 31
    • 82755181676 scopus 로고    scopus 로고
    • For large-scale preparations the less expensive (Z)-decenol was used and oxidized to the aldehyde under Swern conditions according to:, R. A. Fernandes, P. Kattanguru, Tetrahedron: Asymmetry 2011, 22, 1930-1935.
    • (2011) Tetrahedron: Asymmetry , vol.22 , pp. 1930-1935
    • Fernandes, R.A.1    Kattanguru, P.2
  • 33
    • 0347129844 scopus 로고    scopus 로고
    • For the formal acetate aldol reaction Nelson developed a chiral Lewis acid catalyzed cycloaddition; however, the alkaloid-catalyzed version worked very well in our case. For the Lewis acid catalyzed version, see:, S. G. Nelson, C. Zhu, X. Shen, J. Am. Chem. Soc. 2004, 126, 14-15.
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 14-15
    • Nelson, S.G.1    Zhu, C.2    Shen, X.3
  • 39
    • 0019424113 scopus 로고
    • Also Sharpless oxidation of the corresponding alcohol results in relatively low yields
    • Also Sharpless oxidation of the corresponding alcohol results in relatively low yields:, B. E. Rossiter, T. Katsuki, K. B. Sharpless, J. Am. Chem. Soc. 1981, 103, 464-465.
    • (1981) J. Am. Chem. Soc. , vol.103 , pp. 464-465
    • Rossiter, B.E.1    Katsuki, T.2    Sharpless, K.B.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.