A short (3–5 steps) synthesis of a racemic and diastereomeric mixture of Matsucoccus sex pheromones (1–3) is described. The key reaction is Lewis acid-mediated cyanation of symmetric tertiary alcohol 6 to afford common intermediate 7.
本文描述了松果体信息素(1-3)的消旋和非对映异构体的短(3-5步)合成。关键反应是
路易斯酸介导的对称叔醇6的
氰化反应,生成常见中间体7。