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Volumn 60, Issue 7, 2004, Pages 1549-1556

About diastereoselective oxidations of ferrocenyl amino alcohols

Author keywords

Alcohol; Diastereoselectivity; Ferrocene; Oxidation

Indexed keywords

AMINOALCOHOL; DEUTERIUM; HYDROXYL GROUP; MANGANESE OXIDE; METHANOL DERIVATIVE;

EID: 0742272058     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2003.12.004     Document Type: Article
Times cited : (18)

References (29)
  • 13
    • 85050443859 scopus 로고
    • p refer to the planar chirality. All the metallocene chiralities were determined according to the nomenclature of Cahn, Ingold and Prelog extended to planar chiralities
    • p refer to the planar chirality. All the metallocene chiralities were determined according to the nomenclature of Cahn, Ingold and Prelog extended to planar chiralities by Schlögl: Schlögl K. Top. Stereochem. 1:1967;39-91.
    • (1967) Top. Stereochem. , vol.1 , pp. 39-91
    • Schlogl, K.1
  • 14
    • 1542744791 scopus 로고    scopus 로고
    • 2. We could not heat the solution or the amine chain would be oxidized into a carboxaldehyde group:
    • 2. We could not heat the solution or the amine chain would be oxidized into a carboxaldehyde group: Malfait S., Pelinski L., Maciejewski L., Brocard J. Synlett. 7:1997;830-832.
    • (1997) Synlett , vol.7 , pp. 830-832
    • Malfait, S.1    Pelinski, L.2    MacIejewski, L.3    Brocard, J.4
  • 21
    • 85030896930 scopus 로고    scopus 로고
    • 1H NMR spectrum of the mixture of these alcohols was complex, so it did not allow us to determine the proportion of each diastereomer. For this reason the oxidation needed to be performed separately on each compound
    • 1H NMR spectrum of the mixture of these alcohols was complex, so it did not allow us to determine the proportion of each diastereomer. For this reason the oxidation needed to be performed separately on each compound.
  • 27
    • 33947087421 scopus 로고
    • A study on a similar ferrocenic amino alcohol was made and highlighted the preferential conformation of each diastereomer and the nature of the intramolecular hydrogen bond:
    • A study on a similar ferrocenic amino alcohol was made and highlighted the preferential conformation of each diastereomer and the nature of the intramolecular hydrogen bond: Battelle L.F., Bau R., Gokel G.W., Oyakawa R.T., Ugi I.K. J. Am. Chem. Soc. 95:1973;482-486.
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 482-486
    • Battelle, L.F.1    Bau, R.2    Gokel, G.W.3    Oyakawa, R.T.4    Ugi, I.K.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.