Reaction of an anti head-to-tail 4-chlorocoumarin dimer with amines afforded benzopyranocoumarin derivatives in high yields; the reaction is quite different from the expected reaction of coumarin dimer derivatives with amines. On the basis of spectral information, a possible reaction mechanism is pr
Analysis of dimeric species derived from the reaction of phosphatidylethanolamine with dimethylsuberimidate
β Scribed by Mary R. Roth; Fred L. Smardo Jr.; Ruth Welti
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- English
- Weight
- 722 KB
- Volume
- 51
- Category
- Article
- ISSN
- 0009-3084
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β¦ Synopsis
Phosphatidylethanolamines of various fatty acyl species in vortexed lipid dispersions were reacted with dimetbylsuberimidate to produce dimeric products. The yield was 34% at pH 10 and 2% at pH 7. The crosslinked phosphatidylethanolamine species were separated from minor products and the reactants by extraction and two-dimensional thin-layer chromatography on silica gel G, gel filtration on lipophilic Sephadex, or C~,-reversed phase high-performance liquid chromatography (HPLC). Reversed phase HPLC was also used to resolve the dimers into individual molecular species. Analysis of the dimers revealed the extinction coefficients at 205 nm to be higher than those of the reactant pbosphatidylethanolamines. Proton nuclear magnetic resonance spectroscopy and chemical analysis implied that the dimers contain an amidine group.
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