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Volumn 24, Issue 11, 2005, Pages 2819-2821

Rhenium(I)-catalyzed formation of a carbon-oxygen bond: An efficient transition metal catalytic system for etherification of benzyl alcohols

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOLS; CARBON; CATALYSIS; COMPLEXATION; DEHYDRATION; ETHERS; HEATING; OXYGEN; REACTION KINETICS; RHODIUM; SULFURIC ACID; TRANSITION METALS;

EID: 20444481655     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om049040s     Document Type: Article
Times cited : (43)

References (39)
  • 18
    • 0001714567 scopus 로고
    • Recently, there have been developed several new halide-free etherifications of alcohols; for examples, see: (a) Liotta, J. L.; Ganem, B. Tetrahedron Lett. 1989, 30, 4759.
    • (1989) Tetrahedron Lett. , vol.30 , pp. 4759
    • Liotta, J.L.1    Ganem, B.2
  • 32
    • 20444455705 scopus 로고    scopus 로고
    • note
    • 13C NMR and GC-MS spectroscopies by comparison with the authentic samples.
  • 33
    • 20444461853 scopus 로고    scopus 로고
    • note
    • Under the same reaction conditions, the reaction of benzyl alcohol with fert-butyl alcohol afforded the corresponding benzyl tert-butyl ether in only 31% GC yield. In this case, isobutylene formed from the dehydration of tert-butyl alcohol, and the conversion of tert-butyl alcohol reached 82%.
  • 37


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.