Synthesis of lipophilic 3-hydroxy-2-methyl-4-pyridinone derivatives

Article abstract of DOI:10.1080/00397919508015476

Hydrophilic 2-hydroxy-3-methyl-4-pyridinone derivatives were acylated with either long chain acid chlorides or with 1,3,5-benzenetricarbonyl trichloride. The products are either partially lipophilic, bidentatate or hexadentate chelators that form strong 3:1 and 1:1 complexes, respectively, with Fe(III).

Full text of DOI:10.1080/00397919508015476

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Synthetic Communications: An
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Communication of Synthetic
Organic Chemistry
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Synthesis of Lipophilic 3-
Hydroxy-2-methyl-4-pyridinone
Derivatives
G. Liu a , S. C. Miller a & F. W. Bruenger a
a Division of Radiobiology , School of Medicine,
University of Utah , Bldg 585, Salt Lake City, UT,
84112, U.S.A.
Published online: 23 Sep 2006.
To cite this article: G. Liu , S. C. Miller & F. W. Bruenger (1995) Synthesis of
Lipophilic 3-Hydroxy-2-methyl-4-pyridinone Derivatives, Synthetic Communications:
An International Journal for Rapid Communication of Synthetic Organic Chemistry,
25:20, 3247-3253, DOI: 10.1080/00397919508015476
To link to this article: http://dx.doi.org/10.1080/00397919508015476
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