Synthesis of α-aryl-substituted and conformationally restricted fosmidomycin analogues as promising antimalarials

Abstract

Fosmidomycin represents a new antimalarial drug that acts by inhibition of 1-deoxy-D-xylulose 5-phosphate reductoisomerase, an essential enzyme of the mevalonate-independent pathway of isoprenoid biosynthesis. This work describes the synthesis of a series of α-aryl-substituted fosmidomycin analogues that exhibit improved antimalarial activity. A linear synthetic route involving a 3-aryl-3-phosphorylpropanal intermediate proved practical to prepare these derivatives. A phospha-Michael addition to cyclopent-2-enone gave access to conformationally restricted analogues. © Wiley-VCH Verlag GmbH & Co. KGaA, 2006.