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Volumn 69, Issue 4, 2004, Pages 1353-1356

Preparation of Bicyclo[3.2.0]heptane-2-endo,7-endo-diols: 1,3-Diols with a Chiral Rigid Backbone

Author keywords

[No Author keywords available]

Indexed keywords

KETONES; STEREOCHEMISTRY; SYNTHESIS (CHEMICAL);

EID: 1242307322     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo035324v     Document Type: Article
Times cited : (9)

References (30)
  • 3
    • 1242336250 scopus 로고    scopus 로고
    • ENICHEM S.p. A.-Istituto G. Donegani S.p.A.- Eur. Patent Spec. No. 922001957.5-Pub. No. 0521 571 B1 (Sep13, 1995); US Patent no. 5,191,125 (Mar 2, 1993)
    • Rosini, G.; Serra, R.; Rama, F.; Confalonieri, G. ENICHEM S.p. A.-Istituto G. Donegani S.p.A.- Eur. Patent Spec. No. 922001957.5-Pub. No. 0521 571 B1 (Sep13, 1995); US Patent no. 5,191,125 (Mar 2, 1993).
    • Rosini, G.1    Serra, R.2    Rama, F.3    Confalonieri, G.4
  • 8
    • 6844254241 scopus 로고
    • These unsaturated bicyclic lactones are key intermediates for the preparation of linearly condensed triquinane sesquiterpenes according to the elegant Curran's radical cascade methodology: Curran, D. P.; Rakiewicz, D. M. J. Am. Chem. Soc. 1985, 107, 1448; Tetrahedron 1985, 41, 3943.
    • (1985) J. Am. Chem. Soc. , vol.107 , pp. 1448
    • Curran, D.P.1    Rakiewicz, D.M.2
  • 9
    • 0022405113 scopus 로고
    • These unsaturated bicyclic lactones are key intermediates for the preparation of linearly condensed triquinane sesquiterpenes according to the elegant Curran's radical cascade methodology: Curran, D. P.; Rakiewicz, D. M. J. Am. Chem. Soc. 1985, 107, 1448; Tetrahedron 1985, 41, 3943.
    • (1985) Tetrahedron , vol.41 , pp. 3943
  • 16
    • 77953800299 scopus 로고
    • Ojima, I., Ed.; Verlag: New York; Wiley-VCH: New York
    • (b) Asymmetric Synthesis, 2nd ed.; Ojima, I., Ed.; Verlag: New York, 1993; Wiley-VCH: New York, 2000.
    • (1993) Asymmetric Synthesis, 2nd Ed.
  • 17
    • 0003445429 scopus 로고    scopus 로고
    • Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer: Heidelberg
    • (c) Comprehensive Asymmetric Catalysis; Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer: Heidelberg, 1999.
    • (1999) Comprehensive Asymmetric Catalysis
  • 29
    • 1242268705 scopus 로고    scopus 로고
    • note
    • The carbonate moiety acts as a temporary tether. The reaction generates two new stereo centres in one step, through an intramolecular process.
  • 30
    • 1242268709 scopus 로고    scopus 로고
    • note
    • Crystallographic data have been deposited with the Cambridge Crystallographic Data Centre, CCDC number 227177.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.