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Volumn 9, Issue 1, 2007, Pages 141-144

Total synthesis of (-)-blepharocalyxin D

Author keywords

[No Author keywords available]

Indexed keywords

BLEPHAROCALYXIN D; PYRAN DERIVATIVE; UNCLASSIFIED DRUG;

EID: 33846451032     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0627956     Document Type: Article
Times cited : (7)

References (23)
  • 3
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    • A large number of bioactive diarylheptanoid natural products were isolated recently by Kadota and co-workers from the seeds of Alpinia blepharocalyx K. Schum, a member of the Zingiberaceae family: (a) Kadota, S, Prasain, J. K, Li, J. X, Basnet, P, Dong, H, Tani, T, Namba, T. Tetrahedron Lett. 1996, 37, 7283-7286
    • A large number of bioactive diarylheptanoid natural products were isolated recently by Kadota and co-workers from the seeds of Alpinia blepharocalyx K. Schum, a member of the Zingiberaceae family: (a) Kadota, S.; Prasain, J. K.; Li, J. X.; Basnet, P.; Dong, H.; Tani, T.; Namba, T. Tetrahedron Lett. 1996, 37, 7283-7286.
  • 9
    • 33645760404 scopus 로고    scopus 로고
    • More recently, synthetic investigations by Rychnovsky and co-workers led to revised structures of some of the diarylheptanoids, calyxins L, F, M, and G: Tian, X.; Jaber, J. J.; Rychnovsky, S. D. J. Org. Chem. 2006, 71, 3176-3183.
    • More recently, synthetic investigations by Rychnovsky and co-workers led to revised structures of some of the diarylheptanoids, calyxins L, F, M, and G: Tian, X.; Jaber, J. J.; Rychnovsky, S. D. J. Org. Chem. 2006, 71, 3176-3183.
  • 10
    • 33846435404 scopus 로고    scopus 로고
    • 2,8-dioxabicyclo
    • As far as we know, blepharocalyxin D () is the only natural product known to possess a [4.4.0]decane core
    • As far as we know, blepharocalyxin D (1) is the only natural product known to possess a 2,8-dioxabicyclo[4.4.0]decane core.
    • , vol.1
  • 11
    • 0041346083 scopus 로고    scopus 로고
    • There is one reference claiming to be a model study for synthesis of blepharocalyxin D (1): Li, W.; Mead, K. T.; Smith, L. T. Tetrahedron Lett. 2003, 44, 6351-6353.
    • There is one reference claiming to be a model study for synthesis of blepharocalyxin D (1): Li, W.; Mead, K. T.; Smith, L. T. Tetrahedron Lett. 2003, 44, 6351-6353.
  • 15
    • 0001456053 scopus 로고    scopus 로고
    • For extensive use of (O)-acetylmandelate NMR correlation, see: Lee, E.; Lee, Y. R.; Moon, B.; Kwon, O.; Shim, M. S.; Yun, J. S. J. Org. Chem. 1994, 59, 1444-1456.
    • For extensive use of (O)-acetylmandelate NMR correlation, see: Lee, E.; Lee, Y. R.; Moon, B.; Kwon, O.; Shim, M. S.; Yun, J. S. J. Org. Chem. 1994, 59, 1444-1456.
  • 18
    • 22144498082 scopus 로고    scopus 로고
    • For a recent discussion on oxonia-Cope rearrangement, see
    • For a recent discussion on oxonia-Cope rearrangement, see: Jasti, R.; Anderson, C. D.; Rychnovsky, S. D. J. Am. Chem. Soc. 2005, 127, 9939-9945.
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 9939-9945
    • Jasti, R.1    Anderson, C.D.2    Rychnovsky, S.D.3
  • 21
    • 0141678121 scopus 로고    scopus 로고
    • For more discussions on Prins-pinacol reactions, see
    • For more discussions on Prins-pinacol reactions, see: Overman, L. E.; Pennington, L. D. J. Org. Chem. 2003, 68, 7143-7157.
    • (2003) J. Org. Chem , vol.68 , pp. 7143-7157
    • Overman, L.E.1    Pennington, L.D.2
  • 23
    • 0037069714 scopus 로고    scopus 로고
    • For a recent example of the use of lithium alkanethiolate in hot HMPA for aromatic ether demethylation, see: Nakatani, M, Nakamura, M, Suzuki, A, Inoue, M, Katoh, T. Org. Lett. 2002, 4, 4483-4486
    • For a recent example of the use of lithium alkanethiolate in hot HMPA for aromatic ether demethylation, see: Nakatani, M.; Nakamura, M.; Suzuki, A.; Inoue, M.; Katoh, T. Org. Lett. 2002, 4, 4483-4486.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.