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Volumn 14, Issue 24, 2003, Pages 3879-3884

Asymmetric synthesis of macrocyclic binaphthol dimers using a Sonogashira coupling reaction

Author keywords

[No Author keywords available]

Indexed keywords

2,2' BIS(2,2 DICHLORO 1,1 DIFLUOROETHOXY) 1,1' BINAPHTHYL; 3,3' BIS(2 IODOPHENYLETHYNYL) 2,2' BIS(METHOXYMETHOXY) 1,1' BINAPHTHYL; 3,3' BIS(2 IODOPHENYLETHYNYL) 2,2' DIMETHOXY 1,1' BINAPHTHYL; 3,3' BIS(3 IODOPHENYLETHYNYL) 2,2' BIS(METHOXYMETHOXY) 1,1' BINAPHTHYL; 3,3' DIETHYNYL 1,1' BI 2 NAPHTHOL; 3,3' DIETHYNYL 2,2' BIS(METHOXYMETHOXY) 1,1' BINAPHTHYL; 3,3' DIETHYNYL 2,2' DIMETHOXY 1,1' BINAPHTHYL; DIMER; MACROCYCLIC COMPOUND; NAPHTHOL DERIVATIVE; NAPHTHYL GROUP; PHENYL GROUP; UNCLASSIFIED DRUG;

EID: 0344628657     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetasy.2003.09.038     Document Type: Article
Times cited : (10)

References (18)
  • 7
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    • Pu L. Chem. Rev. 98:1998;2405.
    • (1998) Chem. Rev. , vol.98 , pp. 2405
    • Pu, L.1
  • 14
    • 0000509322 scopus 로고
    • B.M. Trost, & I. Fleming. New York: Pergamon Press
    • Sonogashira K. Trost B.M., Fleming I. Comprehensive Organic Synthesis. 3:1991;521 Pergamon Press, New York.
    • (1991) Comprehensive Organic Synthesis , vol.3 , pp. 521
    • Sonogashira, K.1
  • 16
    • 85030931078 scopus 로고    scopus 로고
    • When the coupling reaction leading to 6a was carried out by using 20 mol% of the catalyst and 20 equiv. of 1,2-diiodobenzene, the product yield was improved to 59%.
    • When the coupling reaction leading to 6a was carried out by using 20 mol% of the catalyst and 20 equiv. of 1,2-diiodobenzene, the product yield was improved to 59%.
  • 17
    • 85030922602 scopus 로고    scopus 로고
    • For example, 86% of 1,2-diiodobenzene was recovered in the reaction of 5a.
    • For example, 86% of 1,2-diiodobenzene was recovered in the reaction of 5a.
  • 18
    • 85030919778 scopus 로고    scopus 로고
    • Crystallographic data (excluding structure factors) for the structures in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication numbers CCDC Number: 213427. Copies of the data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge, CB2 1EZ, UK [fax: +44(0)-1223-336033 or e-mail: deposit@ccdc.cam.ac. uk].
    • Crystallographic data (excluding structure factors) for the structures in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication numbers CCDC Number: 213427. Copies of the data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge, CB2 1EZ, UK [fax: +44(0)-1223-336033 or e-mail: deposit@ccdc.cam.ac. uk].


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.