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Volumn 8, Issue 23, 2002, Pages 5377-5383

A novel and useful oxidative intramolecular coupling reaction of phenol ether derivatives on treatment with a combination of hypervalent iodine(III) reagent and heteropoly acid

Author keywords

Biaryls; C C coupling; Heteropoly acids; Hypervalent iodine reagents; Spirodienones

Indexed keywords

DERIVATIVES; ORGANIC ACIDS; OXIDATION; PHENOLS;

EID: 0037011068     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/1521-3765(20021202)8:23<5377::AID-CHEM5377>3.0.CO;2-H     Document Type: Article
Times cited : (96)

References (96)
  • 1
    • 0000942115 scopus 로고
    • For leading references on both the synthesis and the natural occurrence of biaryls, see G. Bringmann. R. Walter, R. Weirich. Angew. Chem. 1990. 102. 1006-1019; Angew. Chem. Int. Ed. Engl. 1990, 29, 977-991.
    • (1990) Angew. Chem. , vol.102 , pp. 1006-1019
    • Bringmann, G.1    Walter, R.2    Weirich, R.3
  • 2
    • 0025164652 scopus 로고
    • For leading references on both the synthesis and the natural occurrence of biaryls, see G. Bringmann. R. Walter, R. Weirich. Angew. Chem. 1990. 102. 1006-1019; Angew. Chem. Int. Ed. Engl. 1990, 29, 977-991.
    • (1990) Angew. Chem. Int. Ed. Engl. , vol.29 , pp. 977-991
  • 3
    • 0007663022 scopus 로고
    • (Ed.: W.S. Trahanovsky), Academic Press, New York
    • O. P. Dhingra in Oxidation in Organic Chemistry; (Ed.: W. S. Trahanovsky), Academic Press, New York, 1982, part D, pp. 207-278.
    • (1982) Oxidation in Organic Chemistry , Issue.PART D , pp. 207-278
    • Dhingra, O.P.1
  • 19
  • 30
    • 0001632656 scopus 로고
    • l) P. J. Stang, Angew. Chem. 1992, 104, 281-292; Angew. Chem. Int. Ed. Engl. 1992, 31, 274-285;
    • (1992) Angew. Chem. , vol.104 , pp. 281-292
    • Stang, P.J.1
  • 31
    • 33748231777 scopus 로고
    • l) P. J. Stang, Angew. Chem. 1992, 104, 281-292; Angew. Chem. Int. Ed. Engl. 1992, 31, 274-285;
    • (1992) Angew. Chem. Int. Ed. Engl. , vol.31 , pp. 274-285
  • 82
    • 0034671861 scopus 로고    scopus 로고
    • b) G. Scheffler, H. Seike, E. J. Sorensen, Angew. Chem. 2000, 112, 4783-4785; Angew. Chem. Int. Ed. 2000, 39, 4593-4596;
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 4593-4596
  • 86
    • 0035902882 scopus 로고    scopus 로고
    • e) M. Node, S. Komada, Y. Hamashita, T. Baba, N. Hamamichi, K. Nishide, Angew. Chem. 2001, 113, 3050-3052; Angew. Chem. Int. Ed. 2001, 40, 3060-3062;
    • (2001) Angew. Chem. Int. Ed. , vol.40 , pp. 3060-3062
  • 91
    • 4243355207 scopus 로고    scopus 로고
    • For recent reviews on heteropoly acids, see: a) I. V. Kozhevnikov, Chem. Rev. 1998, 98, 171-198;
    • (1998) Chem. Rev. , vol.98 , pp. 171-198
    • Kozhevnikov, I.V.1
  • 95
    • 2242455159 scopus 로고    scopus 로고
    • see ref. [6a]
    • There is an example of isolated spirodienones from the siloxy derivatives: see ref. [6a].


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.