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17
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0009682113
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submitted
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The detailed synthesis of closely related dendrimers will be described elsewhere: C. Grandjean, C. Rommens, H. Gras-Masse, and O. Melnyk, J. Chem. Soc., Perkin Trans 1, submitted.
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J. Chem. Soc., Perkin Trans 1
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Grandjean, C.1
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Gras-Masse, H.3
Melnyk, O.4
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84987210276
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Richardson, A.C.3
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19
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0009678101
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The syntheses have been carried out at a 1-4 μmolar scale using degassed solvents and in the dark, when compounds were labelled. The homogeneity of all compounds has been controlled by analytical C18-RP-HPLC or analytical Capillary Zone Electrophoresis. Compounds were characterized by mass electrospray (performed on a Micromass Quatro II Electrospray Mass Spectrometer) and NMR spectra (recorded on Bruker DRX 300 and DRX 600 spectrometers)
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The syntheses have been carried out at a 1-4 μmolar scale using degassed solvents and in the dark, when compounds were labelled. The homogeneity of all compounds has been controlled by analytical C18-RP-HPLC or analytical Capillary Zone Electrophoresis. Compounds were characterized by mass electrospray (performed on a Micromass Quatro II Electrospray Mass Spectrometer) and NMR spectra (recorded on Bruker DRX 300 and DRX 600 spectrometers).
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20
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0030979486
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13C NMR spectra of this compound and compound 10. These data are compatible with those given in the literature, for example: B. G. Shearer, S. Lee, J. A. Oplinger, L. W. Frick, E. P. Garvey, and E. S. Furfine, J. Med. Chem., 1997, 40, 1901-1905.
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Shearer, B.G.1
Lee, S.2
Oplinger, J.A.3
Frick, L.W.4
Garvey, E.P.5
Furfine, E.S.6
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21
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0031662220
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(a) O. Melnyk, M. Bossus, D. David, C. Rommens, and H. Gras-Masse, J. Pept. Res., 1998, 52, 180-184;
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Melnyk, O.1
Bossus, M.2
David, D.3
Rommens, C.4
Gras-Masse, H.5
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22
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0009716643
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in the press
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(b) D. Bonnet, F. Samson, C. Rommens, H. Gras-Masse, and O. Melnyk, J. Pept. Res., 1999, 53, in the press.
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Bonnet, D.1
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Melnyk, O.5
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