Total Synthesis of Biologically Active Natural Products Involving Asymmetric Induction Using Chiral Catalysis

Abstract

We have described herein enantioselective approaches for the synthesis of (+)-serinolamide A, (-)-haliclamide, (+)-petromyroxol, (+)-phomonol, (+)-epi-muricatacin and (-)-6-acetoxy-hexadecanolide employed Trost s DYKAT, MacMillan organocatalyzed aldol reaction, Sharpless AD and Jacobsen s HKR reactions as key steps.. The merits of these synthetic approaches are high enantio- and diastereoselectivity with high yielding reaction steps. All the new compounds were characterized by 1H-NMR, 13C NMR, HRMS, %ee by chiral HPLC and [and#945;]D25 for all new chiral compounds. newline