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Volumn 29, Issue 1, 2005, Pages 173-181

Monophasic and biphasic hydrosilylations of enones and ketones using a fluorous rhodium catalyst that is easily recycled under fluorous-organic liquid-liquid biphasic conditions

Author keywords

[No Author keywords available]

Indexed keywords

2 CYCLOHEXENONE; 2 CYCLOPENTEN 1 ONE; 4,4 DIMETHYL 2 CYCLOHEXEN 1 ONE; CYCLOHEXANONE; CYCLOHEXYLDIMETHYLPHENYLSILYL ETHER; ETHER DERIVATIVE; FLUORINE DERIVATIVE; KETONE DERIVATIVE; ORGANIC COMPOUND; RHODIUM COMPLEX; UNCLASSIFIED DRUG;

EID: 13244253633     PISSN: 11440546     EISSN: None     Source Type: Journal    
DOI: 10.1039/b415344h     Document Type: Article
Times cited : (18)

References (45)
  • 2
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    • (2004) Handbook of Fluorous Chemistry , pp. 24-40
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    • eds. J. A. Gladysz, D. P. Curran and I. T. Horváth, Wiley-VCH, Weinheim
    • I. T. Horváth, in Handbook of Fluorous Chemistry, eds. J. A. Gladysz, D. P. Curran and I. T. Horváth, Wiley-VCH, Weinheim, 2004, pp. 5-10.
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    • note
    • (b) See also ch. 10.8-10.14 in ref. 1.
  • 11
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    • eds. M. Beller and C. Bolm, Wiley-VCH, Weinheim and New York, ch. 1.4.2
    • Reviews covering rhodium-catalyzed hydrosilylations of carbonyl compounds: (a) H. Brunner, in Transition Metals for Organic Synthesis, eds. M. Beller and C. Bolm, Wiley-VCH, Weinheim and New York, 1998, vol. 2, ch. 1.4.2;
    • (1998) Transition Metals for Organic Synthesis , vol.2
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    • 13244253108 scopus 로고    scopus 로고
    • eds. J. A. Gladysz, D. P. Curran and I. T. Horváth, Wiley-VCH, Weinheim
    • (b) J. A. Gladysz and C. Emnet, in Handbook of Fluorous Chemistry, eds. J. A. Gladysz, D. P. Curran and I. T. Horváth, Wiley-VCH, Weinheim, 2004, pp. 11-23.
    • (2004) Handbook of Fluorous Chemistry , pp. 11-23
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    • note
    • Furthermore, solutes often raise the temperatures at which mixing occurs.
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    • (a) For another reaction that yields a 4/5 mixture (both isomers were isolated), see: M. Koreeda and S. Koo, Tetrahedron Lett., 1990, 31, 831;
    • (1990) Tetrahedron Lett. , vol.31 , pp. 831
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    • note
    • 2 proton of 5 or 8;
  • 36
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    • eds. J. A. Gladysz, D. P. Curran and I. T. Horváth, Wiley-VCH, Weinheim
    • J. A. Gladysz, C. Emnet and J. Rábai, in Handbook of Fluorous Chemistry, eds. J. A. Gladysz, D. P. Curran and I. T. Horváth, Wiley-VCH, Weinheim, 2004, pp. 56-100.
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  • 41
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    • (a) I. Ojima, in The Chemistry of Organic Silicon Compounds, eds. S. Patai and Z. Rappoport, Wiley, New York, 1989, vol. 1, part 2, pp. 1491-1492;
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    • note
    • f8 were conducted analogously.
  • 45
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    • note
    • Additional details are given in ref. 13.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.