[摘要]:The prepn. of the C1-C11 subunit I of phoslactomycins, and a formal synthesis of phoslactomycin B, were achieved by a convergent strategy involving the chelation-controlled addn. of an alkynyl Grignard reagent to an a-alkoxy ketone. Catalytic enantioselective redns. of acetylenic ketones and a [2,3]-Wittig rearrangement were utilized as key steps to control the configuration of the C4, C5, and C9 stereocenters.