Synthesis of metal-chelating polymerizable phospholipids

Article abstract of DOI:10.1080/00397919508011392

Two routes for the synthesis of metal chelating phospholipids are reported. An iminodiacetic acid functionality served as metal chelating site in the polar headgroup region of a phospholipid while a tricosa-10,12-diynoyl group linked to the glycerol backbone, made up the polymerizable hydrocarbon region.

Full text of DOI:10.1080/00397919508011392

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Synthesis of Metal-Chelating
Polymerizable Phospholipids
b
a
b
Alok Singh , L.-I. Tsao & Dhananjay B. Puranik
a
Center for Bio/Molecular Science and Engineering,
Naval Research Laboratory , Washington, DC,
2
0375-5438
b
Department of Biochemistry , Georgetown
University , Washington, DC, 20040
Published online: 23 Sep 2006.
To cite this article: Alok Singh , L.-I. Tsao & Dhananjay B. Puranik (1995) Synthesis
of Metal-Chelating Polymerizable Phospholipids, Synthetic Communications: An
International Journal for Rapid Communication of Synthetic Organic Chemistry, 25:4,
573-586, DOI: 10.1080/00397919508011392
To link to this article: http://dx.doi.org/10.1080/00397919508011392
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