Abstract
AbstractObjectiveSynthesis of novel aromatic Lipoxin A4 lactone analogues.ResultsNovelpara-substituted aromatic lactone analogues of Lipoxin A4 have been synthesized in a convergent manner with six steps in the longest linear sequence in 12–13% yields, employing 2-deoxy-d-ribose as a chiral pool starting material and the classicalE-selective Wittig olefination.
Funder
Olav Thon Foundation
UiT, Department of Chemistry
Publication fund of UiT The arctic university of Norway
UiT The Arctic University of Norway
Publisher
Springer Science and Business Media LLC
Subject
General Biochemistry, Genetics and Molecular Biology,General Medicine
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