Wei Wei, Dai Xi-Jie, Wang Haining, Li Chenchen, Yang Xiaobo, Li Chao-Jun
Department of Chemistry , FQRNT Center for Green Chemistry and Catalysis , McGill University , 801 Sherbrooke St. W. , Montreal , Quebec H3A 0B8 , Canada . Email:
School of Chemistry and Chemical Engineering , Qufu Normal University , Qufu 273165 , Shandong , China.
Chem Sci. 2017 Dec 1;8(12):8193-8197. doi: 10.1039/c7sc04207h. Epub 2017 Oct 9.
Natural availability of carbonyl groups offers reductive carbonyl coupling tremendous synthetic potential for efficient olefin synthesis, yet the catalytic carbonyl cross-coupling remains largely elusive. We report herein such a reaction, mediated by hydrazine under ruthenium(ii) catalysis. This method enables facile and selective cross-couplings of two unsymmetrical carbonyl compounds in either an intermolecular or intramolecular fashion. Moreover, this chemistry accommodates a variety of substrates, proceeds under mild reaction conditions with good functional group tolerance, and generates stoichiometric benign byproducts. Importantly, the coexistence of KO Bu and bidentate phosphine dmpe is vital to this transformation.
羰基的天然可利用性为高效烯烃合成提供了还原羰基偶联巨大的合成潜力,但催化羰基交叉偶联在很大程度上仍然难以捉摸。我们在此报告了这样一种反应,该反应由肼在钌(II)催化下介导。这种方法能够以分子间或分子内方式实现两种不对称羰基化合物的简便且选择性交叉偶联。此外,这种化学方法适用于多种底物,在温和的反应条件下进行,具有良好的官能团耐受性,并产生化学计量的良性副产物。重要的是,叔丁醇钾(KO Bu)和双齿膦dmpe的共存对这种转化至关重要。