Synthesis of Optically Active Flower-inducing Fatty Acids, KODA Analogs

立体选择性地合成了有前景的花诱导脂肪酸，Koda类似物，旨在通过手性砜和醛之间的偶联来获得所需的立体异构体。两个段的耦合和随后的组装提供了所需的模拟。这一策略使得合成剩余的立体异构体类似物成为可能。通过利用合成的Koda类似物，Koda诱导开花活性的机理研究和诱导开花调节剂的开发有望取得进展。

Stereoselective synthesis of promising flower-inducing fatty acids, KODA analogs, was designed to obtain the desired stereoisomer viacoupling between chiral sulfone and aldehyde segments. Coupling of the both segments and subsequent assembly gave the desired analog. This strategy made it possible to synthesize the remaining stereoisomeric analogs. By using synthetic KODA analogs, the study of mechanistic elucidation of flower-inducing activity by KODA and the development of flower-inducing regulator are expected to progress.