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.
Keywords: Aromatics; Lactones; Lipoxin analogues; Wittig olefination.
© 2022. The Author(s).