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2
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0037067541
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See for example:
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See for example: Shu-Li Y., Xue-Long X., Li-Xin D., Yi-Hua Y., Wei X. J. Org. Chem. 67:2002;4684-4695.
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(2002)
J. Org. Chem.
, vol.67
, pp. 4684-4695
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Shu-Li, Y.1
Xue-Long, X.2
Li-Xin, D.3
Yi-Hua, Y.4
Wei, X.5
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7
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0036966847
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See for example:
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See for example: Boyd R.B., Sharma N.D., Ljubez V., Byrne B.E., Shepherd A.D., Allen C.C.R., Kulakov L.A., Larkin J.M., Dalton H. Chem. Commun. 2002;1914-1915.
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(2002)
Chem. Commun.
, pp. 1914-1915
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Boyd, R.B.1
Sharma, N.D.2
Ljubez, V.3
Byrne, B.E.4
Shepherd, A.D.5
Allen, C.C.R.6
Kulakov, L.A.7
Larkin, J.M.8
Dalton, H.9
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9
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0033618599
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Molinari F., Villa R., Aragozzini F., Leon R., Prazeres D.M.F. Tetrahedron: Asymmetry. 10:1999;3003-3009.
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(1999)
Tetrahedron: Asymmetry
, vol.10
, pp. 3003-3009
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Molinari, F.1
Villa, R.2
Aragozzini, F.3
Leon, R.4
Prazeres, D.M.F.5
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13
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85050443859
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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
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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.
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(1967)
Top. Stereochem.
, vol.1
, pp. 39-91
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Schlogl, K.1
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14
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1542744791
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2. We could not heat the solution or the amine chain would be oxidized into a carboxaldehyde group:
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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.
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(1997)
Synlett
, vol.7
, pp. 830-832
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Malfait, S.1
Pelinski, L.2
MacIejewski, L.3
Brocard, J.4
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15
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0033795697
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For the synthesis of
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For the synthesis of 3 , see: Picart-Goetgheluck S., Delacroix O., Maciejewski L., Brocard J. Synthesis. 10:2000;1421-1426.
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(2000)
Synthesis
, vol.10
, pp. 1421-1426
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Picart-Goetgheluck, S.1
Delacroix, O.2
MacIejewski, L.3
Brocard, J.4
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21
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85030896930
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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
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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.
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24
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0001280652
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Slocum D.W., Engelmann T.R., Ernst C., Jennings C.A., Jones W., Koonsvitsky B., Lewis J., Shenkin P. J. Chem. Educ. 46:1969;144-150.
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(1969)
J. Chem. Educ.
, vol.46
, pp. 144-150
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Slocum, D.W.1
Engelmann, T.R.2
Ernst, C.3
Jennings, C.A.4
Jones, W.5
Koonsvitsky, B.6
Lewis, J.7
Shenkin, P.8
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27
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33947087421
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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:
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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.
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(1973)
J. Am. Chem. Soc.
, vol.95
, pp. 482-486
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Battelle, L.F.1
Bau, R.2
Gokel, G.W.3
Oyakawa, R.T.4
Ugi, I.K.5
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28
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84981903869
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Battelle L.F., Bau R., Gokel G.W., Oyakawa R.T., Ugi I.K. Angew. Chem., Int. Ed. Engl. 11:1972;138-140.
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(1972)
Angew. Chem., Int. Ed. Engl.
, vol.11
, pp. 138-140
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Battelle, L.F.1
Bau, R.2
Gokel, G.W.3
Oyakawa, R.T.4
Ugi, I.K.5
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