Ho Guo-Ming, Zulueta Medel Manuel L, Hung Shang-Cheng
Genomics Research Center, Academia Sinica, 128, Section 2, Academia Road, Taipei, 115, Taiwan.
Nat Commun. 2017 Sep 25;8(1):679. doi: 10.1038/s41467-017-00787-y.
Polypropionates-motifs with alternating methyl and hydroxy groups-are important segments of many natural products possessing high bioactivity and therapeutic value. Synthetic access to these structures remains an area of intensive interest, focusing on the establishment of the contiguous stereocentres and a desire for operational simplicity. Here we report an efficient strategy for the stereoselective assembly of polypropionates with three or four stereocentres through a three-step relay process that include Diels-Alder reaction, silylenol ether hydrolysis and Baeyer-Villiger oxidation. The stereochemistry and functionality of the resulting polypropionates depend on the substitution pattern of the diene and dienophile substrates of the Diels-Alder cycloaddition. More importantly, the relay sequence is effectively performed in one pot, and the product could potentially undergo the same sequence for further elaboration. Finally, the C1-C9 segment of the macrolide etnangien is constructed with four of the six stereogenic centres established using the relay sequence.Polypropionates are present in many natural products possessing high bioactivity and therapeutic value. Here the authors show a strategy for the stereoselective assembly of polypropionates with three or four stereocentres through a process that includes a Diels-Alder reaction, silylenol ether hydrolysis and Baeyer-Villiger oxidation.
具有交替甲基和羟基的聚丙酸酯基序是许多具有高生物活性和治疗价值的天然产物的重要组成部分。合成这些结构的方法仍然是一个备受关注的领域,重点在于建立连续的立体中心以及追求操作简便性。在此,我们报道了一种通过三步接力过程对具有三个或四个立体中心的聚丙酸酯进行立体选择性组装的有效策略,该过程包括狄尔斯-阿尔德反应、硅烯醇醚水解和拜耳-维利格氧化。所得聚丙酸酯的立体化学和官能团取决于狄尔斯-阿尔德环加成反应中双烯体和亲双烯体底物的取代模式。更重要的是,接力序列可以在一个反应瓶中有效进行,并且产物有可能经历相同的序列进行进一步衍生。最后,使用该接力序列建立了六个立体中心中的四个,从而构建了大环内酯类化合物埃坦吉恩的C1-C9片段。聚丙酸酯存在于许多具有高生物活性和治疗价值的天然产物中。在此,作者展示了一种通过包括狄尔斯-阿尔德反应、硅烯醇醚水解和拜耳-维利格氧化的过程对具有三个或四个立体中心的聚丙酸酯进行立体选择性组装的策略。