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Carbon groups, thin layer chromatography

At 0°C, paclitaxel reacts with the carbonates at its most reactrtoydtoxy group. When the nitro function was reduced under mild conditions, using zinc and acetic acid, complete disappearance of the starting dendron and release of the paclitaxel were observed, and these results were supported by thin layer chromatography studies. Proton-NMR ccmed these results and demonstrated complete... [Pg.456]

See other pages where Carbon groups, thin layer chromatography is mentioned: [Pg.558]    [Pg.384]    [Pg.7]    [Pg.469]    [Pg.5]    [Pg.19]    [Pg.72]    [Pg.946]    [Pg.284]    [Pg.267]    [Pg.428]    [Pg.371]    [Pg.1164]    [Pg.547]    [Pg.258]    [Pg.469]    [Pg.72]    [Pg.4]    [Pg.206]    [Pg.2069]    [Pg.5]    [Pg.558]    [Pg.804]    [Pg.296]    [Pg.804]    [Pg.413]    [Pg.302]    [Pg.2]    [Pg.590]    [Pg.142]    [Pg.121]    [Pg.1189]    [Pg.110]    [Pg.826]   
See also in sourсe #XX -- [ Pg.335 ]



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Carbon Group

Carbon layers

Chromatography groups

Layer group

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