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Volumn 51, Issue 35, 2010, Pages 4636-4639

Synthesis of the human aldose reductase inhibitor rubrolide L

Author keywords

Diabetes; Selective bromination; Suzuki Miyaura cross coupling; Vinylogous aldol condensation

Indexed keywords

3 CHLOROTETRONIC ACID; ALDOSE REDUCTASE INHIBITOR; BUTENOLIDE; OXIDOREDUCTASE; RUBROLIDE L; TETRONIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

EID: 77955658884     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2010.06.129     Document Type: Article
Times cited : (47)

References (69)
  • 30
    • 0031057305 scopus 로고    scopus 로고
    • Diacetates of rubrolides A, C, D and E
    • Diacetates of rubrolides A, C, D and E: M. Kotora, and E. Negishi Synthesis 1997 121 128
    • (1997) Synthesis , pp. 121-128
    • Kotora, M.1    Negishi, E.2
  • 35
    • 77955662903 scopus 로고    scopus 로고
    • PCT Int. Appl., WO 2008040097
    • Kumar, N.; Iskander, G. PCT Int. Appl., WO 2008040097, 2008.
    • (2008)
    • Kumar, N.1    Iskander, G.2
  • 37
    • 15444378803 scopus 로고    scopus 로고
    • Recent reviews on misassigned NP structures
    • Recent reviews on misassigned NP structures: K.C. Nicolaou, and S.A. Snyder Angew. Chem., Int. Ed. 44 2005 1012 1044
    • (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 1012-1044
    • Nicolaou, K.C.1    Snyder, S.A.2
  • 39
    • 0029008906 scopus 로고
    • For our own contributions to the correction of NP structures by total synthesis, see
    • For our own contributions to the correction of NP structures by total synthesis, see: J. Boukouvalas, R. Pouliot, and Y. Fréchette Tetrahedron Lett. 36 1995 4167 4170
    • (1995) Tetrahedron Lett. , vol.36 , pp. 4167-4170
    • Boukouvalas, J.1    Pouliot, R.2    Fréchette, Y.3
  • 56
    • 77955658272 scopus 로고    scopus 로고
    • note
    • 5S (m/z): 265.9264, found: 265.9274.
  • 57
    • 51349111666 scopus 로고    scopus 로고
    • Recent review on Suzuki-Miyaura cross coupling
    • Recent review on Suzuki-Miyaura cross coupling: H. Doucet Eur. J. Org. Chem. 2008 2013 2030
    • (2008) Eur. J. Org. Chem. , pp. 2013-2030
    • Doucet, H.1
  • 58
    • 33845912692 scopus 로고    scopus 로고
    • For some recent examples on the Suzuki arylation of related sulfonates, see
    • For some recent examples on the Suzuki arylation of related sulfonates, see: S.J.P. Yoon-Miller, S.M. Opalka, and E.T. Pelkey Tetrahedron Lett. 48 2007 827 830
    • (2007) Tetrahedron Lett. , vol.48 , pp. 827-830
    • Yoon-Miller, S.J.P.1    Opalka, S.M.2    Pelkey, E.T.3
  • 61
    • 77955652948 scopus 로고    scopus 로고
    • note
    • 5S (m/z): 287.9859, found: 287.9867.
  • 64
    • 77955654941 scopus 로고    scopus 로고
    • note
    • 3: C, 58.81; H, 4.04. Found: C, 58.52; H, 4.24.
  • 65
    • 77955664999 scopus 로고    scopus 로고
    • note
    • 4 (m/z): 328.0502, found: 328.0507.
  • 67
    • 77955656464 scopus 로고    scopus 로고
    • note
    • 4 (m/z): 483.8713, found: 483.8702.
  • 69
    • 77955653085 scopus 로고    scopus 로고
    • note
    • 4: C, 43.21; H, 1.92. Found: C, 43.49; H, 2.30.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.