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Volumn 7, Issue 15, 2001, Pages 3298-3304

Dependence of enantioselectivity on the distribution of a chiral hydrogenation catalyst between an aqueous and a micellar phase: Investigations using pulsed field gradient spin echo NMR spectroscopy

Author keywords

Amino acids; Asymmetric catalysis; Diffusion; Hydrogenation; Micelles; NMR spectroscopy

Indexed keywords

CATALYSTS; DIFFUSION; HYDROGENATION; HYDROPHOBICITY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;

EID: 0035800528     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/1521-3765(20010803)7:15<3298::AID-CHEM3298>3.0.CO;2-4     Document Type: Article
Times cited : (23)

References (55)
  • 4
    • 0004279686 scopus 로고    scopus 로고
    • R. Selke, Enantiomer 1997, 2, 415-419. Some exceptions are included that have high enantioselectivity when water is used as the solvent.
    • (1997) Enantiomer , vol.2 , pp. 415-419
    • Selke, R.1
  • 12
    • 0032476780 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 1998, 37, 2851-2853;
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 2851-2853
  • 19
    • 0032509429 scopus 로고    scopus 로고
    • See the following for interesting details about the importance of micelle formation for high enantioselectivity in asymmetric hydrogenation using rhodium(I) complexes with chiral amphiphilic ligands: I. Grassert, U. Schmidt, S. Ziegler, C. Fischer, G. Oehme, Tetrahedron: Asymmetry 1998, 9, 4193-4202;
    • (1998) Tetrahedron: Asymmetry , vol.9 , pp. 4193-4202
    • Grassert, I.1    Schmidt, U.2    Ziegler, S.3    Fischer, C.4    Oehme, G.5
  • 53
    • 33847589792 scopus 로고    scopus 로고
    • Bruker Analytik, D-76287 Rheinstetten, Germany
    • R. Kerssebaum, DOSY Version 1.5.3., Bruker Analytik, D-76287 Rheinstetten, Germany, 1998.
    • (1998) DOSY Version 1.5.3
    • Kerssebaum, R.1
  • 54
    • 33847596980 scopus 로고    scopus 로고
    • note
    • We thank Dr. W. Hintz for the determination of this cmc by the ring method (surface tension).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.