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Volumn , Issue 9, 2000, Pages 1741-1744

Synthesis of medium and large rings, XLVII. Synthesis of heptano bridged pyranoside derivatives

Author keywords

Bridged pyranose derivatives; Carbenes; Glycosides; Ring enlargement

Indexed keywords

CARBENE; GLYCOSIDE; PYRANOSIDE;

EID: 0034026135     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/(sici)1099-0690(200005)2000:9<1741::aid-ejoc1741>3.3.co;2-n     Document Type: Article
Times cited : (7)

References (18)
  • 1
    • 0003891487 scopus 로고    scopus 로고
    • Wiley-VCH, Weinheim, Berlin, New York, Chichester, Toronto, Brisbane, Singapore
    • Carbohydrate Mimics (Ed.: Y. Chapleur), Wiley-VCH, Weinheim, Berlin, New York, Chichester, Toronto, Brisbane, Singapore, 1998.
    • (1998) Carbohydrate Mimics
    • Chapleur, Y.1
  • 5
    • 0342710838 scopus 로고
    • Dissertation, Universität Kiel
    • Compound 2 was first isolated by A.-K. Mattauch, see: A.-K. Mattauch, Dissertation, Universität Kiel, 1995.
    • (1995)
    • Mattauch, A.-K.1
  • 6
    • 0012804434 scopus 로고    scopus 로고
    • Selected recent examples: [6a] S. J. Danishefsky, M. T. Bilodeau, Angew. Chem. 1996, 108, 1483-1522: Angew. Chem. Int. Ed. Engl. 1996, 35, 1380-1419. -
    • (1996) Angew. Chem. , vol.108 , pp. 1483-1522
    • Danishefsky, S.J.1    Bilodeau, M.T.2
  • 7
    • 0029739240 scopus 로고    scopus 로고
    • Selected recent examples: [6a] S. J. Danishefsky, M. T. Bilodeau, Angew. Chem. 1996, 108, 1483-1522: Angew. Chem. Int. Ed. Engl. 1996, 35, 1380-1419. -
    • (1996) Angew. Chem. Int. Ed. Engl. , vol.35 , pp. 1380-1419
  • 11
    • 0342275681 scopus 로고    scopus 로고
    • Dissertation, Universität Kiel
    • V. Kirsch, Dissertation, Universität Kiel, 1999.
    • (1999)
    • Kirsch, V.1
  • 14
    • 0342275679 scopus 로고    scopus 로고
    • Commercial product of Merck KGaA, Darmstadt, Germany
    • Commercial product of Merck KGaA, Darmstadt, Germany.
  • 15
    • 0342275677 scopus 로고    scopus 로고
    • note
    • The volume integrals of the correlation peaks were determined by the program XWIN-NMR of Bruker Analytic GmbH, Karlsruhe, Germany. Calibration of the distances were carried out by standardization of the methylene proton distances of the methoxymethyl group to 178 pm.
  • 18
    • 0343580883 scopus 로고    scopus 로고
    • note
    • Crystallographic data (excluding structure factors) for the structure in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication no. CCDC-137265. 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 or E-mail: deposit@ccdc.cam.ac.uk].


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.