Chemisches Institut, Otto-von-Guericke-Universität, Universitätsplatz 2, 39106 Magdeburg, Germany.
Org Lett. 2021 Jun 18;23(12):4543-4547. doi: 10.1021/acs.orglett.1c01123. Epub 2021 May 26.
Disorazoles represent a powerful class of highly potent antitubulin natural products isolated from myxobacteria. Herein, we describe a scalable and robust synthesis of (-)-disorazole C with high stereoselectivity, featuring quite simple reaction conditions that can be used to produce large quantities of this remarkable biologically active compound.
蝶酸酯类化合物是从粘细菌中分离得到的一类具有强效抗肿瘤活性的微管蛋白抑制剂。在此,我们描述了 (-)-蝶酸酯 C 的一种可规模化、高立体选择性的合成方法,其反应条件非常简单,可用于大量制备这种具有显著生物活性的化合物。