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Volumn , Issue 19, 2001, Pages 3669-3676

Synthesis of highly substituted methylenecyclohexenes using new domino reactions with sultones

Author keywords

Carbenoids; Desulfurization; Domino reactions; Sulfur heterocycles

Indexed keywords

CARBENOID; CYCLOHEXENE DERIVATIVE; SILANE DERIVATIVE; SULTONE;

EID: 0034791734     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/1099-0690(200110)2001:19<3669::AID-EJOC3669>3.0.CO;2-S     Document Type: Article
Times cited : (25)

References (44)
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    • For reviews on sultone chemistry, see: [1a] P. Metz, J. Prakt. Chem. 1998, 340, 1-10.
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    • Metz, P.1
  • 4
    • 0032510338 scopus 로고    scopus 로고
    • For reviews on a related sequence involving intramolecular Diets-Alder reaction of silicon-tethered trienes and subsequent desilylation, see: [2a] D. R. Gauthier, Jr., K. S. Zandi, K. J. Shea, Tetrahedron 1998, 54, 2289-2338.
    • (1998) Tetrahedron , vol.54 , pp. 2289-2338
    • Gauthier Jr., D.R.1    Zandi, K.S.2    Shea, K.J.3
  • 9
    • 0002018106 scopus 로고    scopus 로고
    • A related intermediate featuring a carbanionic center in the endocyclic β-position to the sulfur atom is probably formed in the final step of our sultone route to nonactic acid, see: [4a] U. Meiners, E. Cramer, R. Fröhlich, B. Wibbeling, P. Metz, Eur. J. Org. Chem. 1998, 2073-2078.
    • (1998) Eur. J. Org. Chem. , pp. 2073-2078
    • Meiners, U.1    Cramer, E.2    Fröhlich, R.3    Wibbeling, B.4    Metz, P.5
  • 13
    • 0003206168 scopus 로고    scopus 로고
    • note
    • -3, hydrogen atoms calculated and refined riding, two independent molecules in the asymmetric unit being enantiomers. Crystallographic data (excluding structure factors) for the structure reported in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication no. CCDC-161616. Copies of the data can be obtained free of charge on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK [Fax: (internat.) + 44-1223/336-033; E-mail: deposit@ccdc.cam.ac.uk].
  • 23
    • 0003268745 scopus 로고
    • (Eds.: B. M. Trost, C. R. Hutchinson), Pergamon Press, Oxford
    • [3c] R. H. Schlessinger in Organic Synthesis Today and Tomorrow (Eds.: B. M. Trost, C. R. Hutchinson), Pergamon Press, Oxford, 1981, pp. 251-258.
    • (1981) Organic Synthesis Today and Tomorrow , pp. 251-258
    • Schlessinger, R.H.1
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    • For reviews, see: [17a] L. F. Tietze, Chem. Rev. 1996, 96, 115-136.
    • (1996) Chem. Rev. , vol.96 , pp. 115-136
    • Tietze, L.F.1
  • 44
    • 33847593653 scopus 로고
    • Ph. D. Dissertation, Universität Münster
    • J. Stölting, Ph. D. Dissertation, Universität Münster, 1995.
    • (1995)
    • Stölting, J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.