Department of Chemistry, The Scripps Research Institute , 10550 North Torrey Pines Road, La Jolla, California 92037, United States.
J Am Chem Soc. 2016 Nov 2;138(43):14234-14237. doi: 10.1021/jacs.6b09701. Epub 2016 Oct 19.
A concise route to a small family of exotic marine alkaloids known as the araiosamines has been developed, and their absolute configuration has been assigned. The dense array of functionality, high polarity, and rich stereochemistry coupled with equilibrating topologies present an unusual challenge for chemical synthesis and an opportunity for innovation. Key steps involve the use of a new reagent for guanidine installation, a remarkably selective C-H functionalization, and a surprisingly simple final step that intersects a presumed biosynthetic intermediate. Synthetic araiosamines were shown to exhibit potency against Gram-positive and -negative bacteria despite a contrary report of no activity.
已经开发出一种简洁的方法来合成一组被称为 araiosamines 的海洋生物碱,并且确定了它们的绝对构型。这些化合物具有高度的极性和丰富的立体化学,并且功能密集,拓扑结构不断变化,这对化学合成提出了不寻常的挑战,同时也为创新提供了机会。关键步骤包括使用新的胍基安装试剂、非常选择性的 C-H 官能化以及最后一步的巧妙设计,该步骤与假定的生物合成中间体相交。尽管有报道称 araiosamines 没有活性,但合成的 araiosamines 被证明对革兰氏阳性和阴性细菌具有活性。