Objective: Synthesis of novel aromatic Lipoxin A4 lactone analogues.
Results: Novel para-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 classical E-selective Wittig olefination.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8827294 | PMC |
http://dx.doi.org/10.1186/s13104-022-05917-4 | DOI Listing |
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