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Volumn 59, Issue 2, 2003, Pages 485-490

A stereocontrolled synthesis of (+)-rhopaloic acid a using a dioxabicyclo[3.2.1]octane chiral building block

Author keywords

[No Author keywords available]

Indexed keywords

BICYCLO[3.2.1]OCTANE DERIVATIVE; DIOXABICYCLO[3.2.1]OCTANE; NATURAL PRODUCT; NORSESTERTERPENE; RHOPALOIC ACID A; TERPENE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0037346085     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/com-02-s70     Document Type: Article
Times cited : (13)

References (25)
  • 3
    • 0036554030 scopus 로고    scopus 로고
    • For a pertinent review for utilization of the compound (2) as a versatile chiral building block, see: K. Ogasawara, J. Syn. Org. Chem. Jpn., 2002, 60, 316.
    • (2002) J. Syn. Org. Chem. Jpn. , vol.60 , pp. 316
    • Ogasawara, K.1
  • 5
    • 0030872616 scopus 로고
    • For racemic syntheses, see: a) B. B. Snider and F. He, Tetrahedron Lett., 1977, 38, 5453. b) R. Takagi, A. Sasaoka, S. Kojima, and K. Ohkata, Heterocycles, 1997, 45, 2313. For racemic and non-racemic syntheses, see: c) R. Takagi, A. Sasaoka, S. Kojima, and K. Ohkata, Chem. Commun., 1997, 1887. d) R. Takagi, A. Sasaoka, H. Nishitani, S. Kojima, Y. Hiraga, and K. Ohkata, J. Chem. Soc., Perkin Trans. 1, 1998, 925.
    • (1977) Tetrahedron Lett. , vol.38 , pp. 5453
    • Snider, B.B.1    He, F.2
  • 6
    • 0000103277 scopus 로고    scopus 로고
    • For racemic syntheses, see: a) B. B. Snider and F. He, Tetrahedron Lett., 1977, 38, 5453. b) R. Takagi, A. Sasaoka, S. Kojima, and K. Ohkata, Heterocycles, 1997, 45, 2313. For racemic and non-racemic syntheses, see: c) R. Takagi, A. Sasaoka, S. Kojima, and K. Ohkata, Chem. Commun., 1997, 1887. d) R. Takagi, A. Sasaoka, H. Nishitani, S. Kojima, Y. Hiraga, and K. Ohkata, J. Chem. Soc., Perkin Trans. 1, 1998, 925.
    • (1997) Heterocycles , vol.45 , pp. 2313
    • Takagi, R.1    Sasaoka, A.2    Kojima, S.3    Ohkata, K.4
  • 7
    • 0012519623 scopus 로고    scopus 로고
    • For racemic syntheses, see: a) B. B. Snider and F. He, Tetrahedron Lett., 1977, 38, 5453. b) R. Takagi, A. Sasaoka, S. Kojima, and K. Ohkata, Heterocycles, 1997, 45, 2313. For racemic and non-racemic syntheses, see: c) R. Takagi, A. Sasaoka, S. Kojima, and K. Ohkata, Chem. Commun., 1997, 1887. d) R. Takagi, A. Sasaoka, H. Nishitani, S. Kojima, Y. Hiraga, and K. Ohkata, J. Chem. Soc., Perkin Trans. 1, 1998, 925.
    • (1997) Chem. Commun. , vol.1887
    • Takagi, R.1    Sasaoka, A.2    Kojima, S.3    Ohkata, K.4
  • 8
    • 33748617886 scopus 로고    scopus 로고
    • For racemic syntheses, see: a) B. B. Snider and F. He, Tetrahedron Lett., 1977, 38, 5453. b) R. Takagi, A. Sasaoka, S. Kojima, and K. Ohkata, Heterocycles, 1997, 45, 2313. For racemic and non-racemic syntheses, see: c) R. Takagi, A. Sasaoka, S. Kojima, and K. Ohkata, Chem. Commun., 1997, 1887. d) R. Takagi, A. Sasaoka, H. Nishitani, S. Kojima, Y. Hiraga, and K. Ohkata, J. Chem. Soc., Perkin Trans. 1, 1998, 925.
    • (1998) J. Chem. Soc., Perkin Trans. 1 , vol.925
    • Takagi, R.1    Sasaoka, A.2    Nishitani, H.3    Kojima, S.4    Hiraga, Y.5    Ohkata, K.6
  • 14
    • 0012514613 scopus 로고    scopus 로고
    • note
    • Bis(tricyclohexylphosphine)benzylideneruthenium(IV) dichloride was purchased from Strem Chemicals and used without further purification.
  • 25
    • 85085715787 scopus 로고    scopus 로고
    • 13C NMR, and MS) were identical with those reported to the natural product
    • 13C NMR, and MS) were identical with those reported to the natural product.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.