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Volumn , Issue 9, 1997, Pages 1307-1313

Bicyclo[3.3.1]nonanes as synthetic intermediates. Part 19. Asymmetric cleavage of ω-azabicyclo[3.n.1]alkan-3-ones at the 'fork head'

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EID: 33748647052     PISSN: 0300922X     EISSN: None     Source Type: Journal    
DOI: 10.1039/a607812e     Document Type: Article
Times cited : (38)

References (41)
  • 1
    • 33748587579 scopus 로고    scopus 로고
    • The previous paper entitled 'Tandem Beckmann and Huisgen-White rearrangement as an alternative to the Bayer-Villiger oxidation of the bicyclo[3.3.1]nonane system: First asymmetric synthesis of (-)-dihydropalustramic acid. X-Ray molecular structure of 2β-ethyl-9-phenylsulfonyl-9-azabicyclo[3.3.1]nonan-3-one' [O. Muraoka, B.-Z. Zheng, K. Okumura, G. Tanabe, T. Momose and C. H. Eugster, J. Chem. Soc., Perkin Trans. 1, 1996, 1567]
    • (1996) J. Chem. Soc., Perkin Trans. 1 , pp. 1567
    • Muraoka, O.1    Zheng, B.-Z.2    Okumura, K.3    Tanabe, G.4    Momose, T.5    Eugster, C.H.6
  • 4
    • 77957051048 scopus 로고
    • ed. A. Brossi, Academic Press, New York
    • G. M. Strunz and J. A. Findlay, The Alkaloids, ed. A. Brossi, Academic Press, New York, 1985, vol. 26, p. 89.
    • (1985) The Alkaloids , vol.26 , pp. 89
    • Strunz, G.M.1    Findlay, J.A.2
  • 5
    • 77957031616 scopus 로고
    • ed. G. A. Cordell, Academic Press, San Diego
    • See, for example, H. Takahata and T. Momose, The Alkaloids, ed. G. A. Cordell, Academic Press, San Diego, 1993, vol. 44, pp. 189-256;
    • (1993) The Alkaloids , vol.44 , pp. 189-256
    • Takahata, H.1    Momose, T.2
  • 6
    • 77957031294 scopus 로고
    • ed. A. Brossi, Academic Press, New York
    • A. Numata and T. Ibuka, The Alkaloids, ed. A. Brossi, Academic Press, New York, 1987, vol. 31, pp. 193-315;
    • (1987) The Alkaloids , vol.31 , pp. 193-315
    • Numata, A.1    Ibuka, T.2
  • 24
    • 0026033510 scopus 로고
    • Simpkins' group has also studied similar HCLA (homochiral lithium amide) chemistry, see: P. J. Cox and N. S. Simpkins, Tetrahedron: Asymmetry, 1992, 2, 1.
    • (1992) Tetrahedron: Asymmetry , vol.2 , pp. 1
    • Cox, P.J.1    Simpkins, N.S.2
  • 27
    • 0029115128 scopus 로고
    • Majewski's group has also investigated the enantioselective deprotonation of tropinone using HCLA and reaction of the chiral lithium enolate of tropinone: M. Majewski and R. Lazny, J. Org. Chem., 1995, 60, 5825 and references cited therein.
    • (1995) J. Org. Chem. , vol.60 , pp. 5825
    • Majewski, M.1    Lazny, R.2
  • 28
    • 0012047909 scopus 로고
    • For 9-benzyl-9-azabicyclo[3.3.1]nonan-3-one, see: K. Stach and O. Dold, Arzneim. Forsch., 1962, 12, 1022. The procedure was partially modified in the present work: see Experimental section.
    • (1962) Arzneim. Forsch. , vol.12 , pp. 1022
    • Stach, K.1    Dold, O.2
  • 30
    • 85087582491 scopus 로고    scopus 로고
    • note
    • 1OH(10:1).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.