Xianrong Cai, Jie Xiang, Jia Zheng, Juan Tang, Jian Su, Chunru Cheng
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引用次数: 0
Abstract
An efficient one-pot synthesis of 1,3-diketones has been synthesized starting from alkynones using a Michael addition–nucleophilic substitution reaction process. The reaction starts with the Michael addition of imidazoles to alkynones, followed by the nucleophilic substitution by water. The final product 1,3-diketones were characterized by the NMR spectra. This study demonstrated that such reactions could successfully occur in one pot under mild conditions with a high yield of 1,3-diketones from 65 to 93%.
期刊介绍:
Russian Journal of Organic Chemistry is an international peer reviewed journal that covers all aspects of modern organic chemistry including organic synthesis, theoretical organic chemistry, structure and mechanism, and the application of organometallic compounds in organic synthesis.