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Volumn 131, Issue 30, 2009, Pages 10587-10597

Total synthesis and biological evaluation of cortistatins A and J and analogues thereof

Author keywords

[No Author keywords available]

Indexed keywords

ANTI-PROLIFERATIVE; ANTIPROLIFERATIVE ACTIVITIES; BIOLOGICAL ACTIVITIES; BIOLOGICAL EVALUATION; BUILDING BLOCK; CANCER CELLS; CASCADE REACTIONS; CORTISTATIN A; DIVERGENT APPROACH; EPOXY KETONES; HYDROXYL GROUPS; NATURAL PRODUCTS; NATURALLY OCCURRING; PARENT COMPOUNDS; STEREOSELECTIVE MANNER; SUZUKI-MIYAURA COUPLING REACTION; SYNTHETIC TECHNOLOGY; TARGET MOLECULE; TOTAL SYNTHESIS;

EID: 68049100404     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja902939t     Document Type: Article
Times cited : (99)

References (53)
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    • Carmeliet, P.1
  • 7
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    • For a total synthesis of cortistatin A, see: b
    • For a total synthesis of cortistatin A, see: (b) Lee, H. M.; Nieto-Oberhuber, C.; Shair, M. D. J. Am. Chem. Soc. 2008, 130, 16864-16866.
    • (2008) J. Am. Chem. Soc , vol.130 , pp. 16864-16866
    • Lee, H.M.1    Nieto-Oberhuber, C.2    Shair, M.D.3
  • 8
    • 65549171152 scopus 로고    scopus 로고
    • For a formal synthesis of cortistatin A, see: c
    • For a formal synthesis of cortistatin A, see: (c) Yamashita, S.; Kitajima, K.; Iso, K.; Hirama, M. Tet. Lett. 2009, 50, 3277-3279.
    • (2009) Tet. Lett , vol.50 , pp. 3277-3279
    • Yamashita, S.1    Kitajima, K.2    Iso, K.3    Hirama, M.4
  • 9
    • 53149108274 scopus 로고    scopus 로고
    • For studies toward the synthesis of cortistatins, see: d
    • For studies toward the synthesis of cortistatins, see: (d) Yamashita, S.; Iso, K.; Hirama, M. Org. Lett. 2008, 10, 3413-3415.
    • (2008) Org. Lett , vol.10 , pp. 3413-3415
    • Yamashita, S.1    Iso, K.2    Hirama, M.3
  • 19
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    • For a recentreview on cascade reactions in total synthesis, see: a
    • For a recentreview on cascade reactions in total synthesis, see: (a) Nicolaou, K. C.; Montagnon, T.; Snyder, S. A. Chem. Commun. 2003, 5, 551-564.
    • (2003) Chem. Commun , vol.5 , pp. 551-564
    • Nicolaou, K.C.1    Montagnon, T.2    Snyder, S.A.3
  • 25
    • 0027234426 scopus 로고    scopus 로고
    • For the synthesis of ent-14, see: (b) Isaacs, R. C. A.; Di Grandi, M. J.; Danishefsky, S. J. J. Org. Chem. 1993, 58, 3938-3941.
    • For the synthesis of ent-14, see: (b) Isaacs, R. C. A.; Di Grandi, M. J.; Danishefsky, S. J. J. Org. Chem. 1993, 58, 3938-3941.
  • 38
    • 68049097894 scopus 로고    scopus 로고
    • CCDC-710299 and CCDC-710298 containthe supplementary crystallographic data for compounds 34 and 36, respectively. These data can be obtained freeof charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
    • CCDC-710299 and CCDC-710298 containthe supplementary crystallographic data for compounds 34 and 36, respectively. These data can be obtained freeof charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
  • 40
    • 0001443466 scopus 로고    scopus 로고
    • Prepared from 7-bromoisoquinoline via:[Pd(dppf)Cl2], KOAc, bispinacolato diboron, DMSO, 80 ° C,50%. For preparation of 7-bromoisoquinoline, see: Miller, B. R.; Frincke, J. M. J. Org. Chem. 1980, 45, 5312-5315.
    • Prepared from 7-bromoisoquinoline via:[Pd(dppf)Cl2], KOAc, bispinacolato diboron, DMSO, 80 ° C,50%. For preparation of 7-bromoisoquinoline, see: Miller, B. R.; Frincke, J. M. J. Org. Chem. 1980, 45, 5312-5315.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.