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Volumn , Issue 8, 2009, Pages 1295-1298

A practical and highly chemoselective hydrogenation of aldehydes with a copper catalyst

Author keywords

Aldehydes; Chemoselectivity; Copper; Homogeneous catalysis; Hydrogenation

Indexed keywords

1,4 BIS(DIPHENYLPHOSPHINO)BUTANE; ALCOHOL; ALDEHYDE DERIVATIVE; BIPHOSPHINE; BUTANE; COPPER; PHOSPHINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 67649410249     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0028-1216726     Document Type: Article
Times cited : (28)

References (15)
  • 2
    • 84889336887 scopus 로고    scopus 로고
    • Surburg, H.; Panten, J., Eds.; Wiley-VCH: Weinheim
    • (b) Common Fragrance and Flavor Materials; Surburg, H.; Panten, J., Eds.; Wiley-VCH: Weinheim, 2006.
    • (2006) Common Fragrance and Flavor Materials
  • 5
    • 33644640381 scopus 로고    scopus 로고
    • Recent review: de Vries, J. G.; Elsevier, C. J., Eds.; Wiley-VCH: Weinheim, Chap. 15
    • Recent review: Clarke, M. L.; Roff, G. J. Handbook of Homogeneous Hydrogenation, Vol.1; de Vries, J. G.; Elsevier, C. J., Eds.; Wiley-VCH: Weinheim, 2007, Chap. 15, 413-454.
    • (2007) Handbook of Homogeneous Hydrogenation , vol.1 , pp. 413-454
    • Clarke, M.L.1    Roff, G.J.2
  • 12
    • 67649413647 scopus 로고    scopus 로고
    • note
    • Our attempt to hydrogenate (-)-4-(prop-1-en-2-yl)cyclohexen-1- carbaldehyde [(-)-perilaldehyde] at S/C = 500 with the condition described in ref. 6b, resulted in trace conversion. The reaction reportedly completed at S/C = 20, which was reproduced by us.
  • 15
    • 67649409277 scopus 로고    scopus 로고
    • note
    • 2O-hexane = 1:1) after removal of the solvent gave (E)-2-methyl-3-phenylprop-2-en-1-ol (1.32 g, 99%, E/Z = 99:1).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.