Qin Rui, Yu Ting-Ting, Liu Shuai-Jiang, Wang You-Cheng, Luo Meng-Lan, Chen Ben-Hong, Zhao Qian, Huang Wei
State Key Laboratory of Southwestern Chinese Medicine Resources, School of Basic Medical Sciences, School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, China.
J Org Chem. 2022 Apr 15;87(8):5358-5370. doi: 10.1021/acs.joc.2c00187. Epub 2022 Mar 24.
Although numerous chiral pyrazolones with a six-membered spirocyclic center at the C4 position have been developed, the asymmetric construction of six-membered oxa-spiropyrazolones is still a challenging task in organic synthesis. Herein, we describe the [4 + 2] annulation of cyclobutanones and pyrazoline-4,5-diones for the efficient synthesis of δ-lactone-fused spiropyrazolone derivatives with generally high yields and good enantioselectivities under mild conditions. The successful scale-up synthesis and further transformation of the final product highlight the practicality and reliability of this reaction.
尽管已经开发出了许多在C4位置具有六元螺环中心的手性吡唑啉酮,但六元氧杂螺吡唑啉酮的不对称构建在有机合成中仍然是一项具有挑战性的任务。在此,我们描述了环丁酮与吡唑啉-4,5-二酮的[4 + 2]环化反应,用于在温和条件下高效合成具有普遍高产率和良好对映选择性的δ-内酯稠合螺吡唑啉酮衍生物。最终产物的成功放大合成和进一步转化突出了该反应的实用性和可靠性。