Total synthesis of the endogenous inflammation resolving lipid resolvin D2 using a common lynchpin

Abstract

The total synthesis of the endogenous inflammation resolving eicosanoid resolvin D2 (1) is described. The key steps involved a Wittig reaction between aldehyde 5 and the ylide derived from phosphonium salt 6 to give enyne 17 and condensation of the same ylide with aldehyde 7 to afford enyne 11. Desilylation of 11 followed by hydrozirconation and iodination gave the vinyl iodide 4 and Sonogashira coupling between this compound and enyne 3 provided alkyne 18. Acetonide deprotection, partial reduction and ester hydrolysis then gave resolvin D2 (1).

Keywords

• catalysis
• eicosanoid
• natural product
• resolvin D2
• Sonogashira coupling
• total synthesis
• Wittig reaction