Abstract The synthesis of Lipoxin B 4 analogs (LXB ) to gain access stabilized inflammation resolving compounds is an actual field research. Focusing on variation and stabilization the conjugated E,Z,E,E C6–C13 tetraene moiety natural LXB , a methylene bridge introduced between C6 C11 suppresses any Z/E isomerization C8–C9 olefin. Intending enable prospective structure variations in connection ...