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Volumn , Issue 6, 2000, Pages 847-849

Fluorous biphase catalytic Friedel-Crafts acylation: Ytterbium tris(perfluoroalkanesulfonyl)methide catalysts

Author keywords

Acylation; Catalysis; Fluorous phase; Methide; Ytterbium

Indexed keywords

ACID ANHYDRIDE; ANISOLE; POLYCYCLIC AROMATIC HYDROCARBON; YTTERBIUM;

EID: 0034099612     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (55)

References (26)
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    • Kawada, A.; Mitamura, S.; Kobayashi, S. J. Chem. Soc. Chem. Commun. 1993, 1157; Kawada, A.; Mitamura, S.; Kobayashi, S. Synlett 1994, 545; Hachiya, I.; Moriwaki, M.; Kobayshi, S. Bull. Chem. Soc. Jpn. 1995, 68, 2053; Kobayashi, S.; Iwamoto, S. Tetrahedron Lett. 1998, 39, 4697.
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    • Kawada, A.; Mitamura, S.; Kobayashi, S. J. Chem. Soc. Chem. Commun. 1993, 1157; Kawada, A.; Mitamura, S.; Kobayashi, S. Synlett 1994, 545; Hachiya, I.; Moriwaki, M.; Kobayshi, S. Bull. Chem. Soc. Jpn. 1995, 68, 2053; Kobayashi, S.; Iwamoto, S. Tetrahedron Lett. 1998, 39, 4697.
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    • note
    • 13C NMR and by MS.
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    • note
    • 2 (5 mL). The layers were separated and an aliquot was removed from the organic layer and analysed by GC/MS (82% conversion). The organics were extracted with hot (ca 85 °C) perfluoromethyldecalin (3 × 5 mL). The combined fluorous extracts were evaporated to give recovered 7d (96%).
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    • note
    • Catalytic Compounds and Processes. UK application 9919583.6.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.