Emmons-Horner reactions of various α-alkoxyphosphonoacetates were examined. The latter reactions proceeded with considerable stereoselectivity, which allowed the efficient preparation of an intermediate in cytochalasin synthesis.
检查了各种α-烷氧基
膦酸酯的制备和Emmons-Horner反应。后面的反应以相当大的立体选择性进行,这允许有效制备细胞
松弛素合成中的中间体。