Department of Chemistry, The Scripps Research Institute, 10550 N. Torrey Pines Road, La Jolla, California 92037, United States.
J Am Chem Soc. 2023 Jun 21;145(24):13003-13007. doi: 10.1021/jacs.3c03378. Epub 2023 Jun 7.
1,3-Dienes are common scaffolds in biologically active natural products as well as building blocks for chemical synthesis. Developing efficient methods for the synthesis of diverse 1,3-dienes from simple starting materials is therefore highly desirable. Herein, we report a Pd(II)-catalyzed sequential dehydrogenation reaction of free aliphatic acids via β-methylene C-H activation, which enables one-step synthesis of diverse -1,3-dienes. Free aliphatic acids of varying complexities, including the antiasthmatic drug seratrodast, were found to be compatible with the reported protocol. Considering the high lability of 1,3-dienes and lack of protecting strategies, dehydrogenation of aliphatic acids to reveal 1,3-dienes at the late stage of synthesis offers an appealing strategy for the synthesis of complex molecules containing such motifs.
1,3-二烯是生物活性天然产物中的常见支架,也是化学合成的构建块。因此,开发从简单起始原料高效合成各种 1,3-二烯的方法是非常需要的。在此,我们报告了一种通过β-亚甲基 C-H 活化的 Pd(II)催化的游离脂肪酸的顺序脱氢反应,该反应能够一步合成各种 -1,3-二烯。各种复杂程度的游离脂肪酸,包括抗哮喘药物色甘酸钠,都与所报道的方案兼容。考虑到 1,3-二烯的高不稳定性和缺乏保护策略,在合成后期将脂肪酸脱氢以揭示 1,3-二烯为反应提供了一种吸引人的策略,用于合成含有此类结构的复杂分子。