Department of Environmental Science, Graduate School of Fisheries and Environmental Sciences, Nagasaki University, 1-14 Bunkyo-machi, Nagasaki, 852-8521, Japan.
Department of Chemistry and Research Center for Smart Molecules, Faculty of Science, Rikkyo University, 3-34-1, Nishi-Ikebukuro, Toshima-ku, Tokyo, 171-8501, Japan.
Chemistry. 2018 Nov 13;24(63):16747-16752. doi: 10.1002/chem.201803703. Epub 2018 Oct 26.
Although a wide variety of chiral organocatalysts have been developed for asymmetric transformations, effective chiral dialkyl sulfide organocatalysts remain relatively rare and under-developed, despite the potential utility of dialkyl sulfide catalysts. Herein, we report the development of chiral bifunctional dialkyl sulfide catalysts possessing a urea moiety for regio-, diastereo-, and enantioselective bromolactonization. The importance of the bifunctional design of chiral sulfide catalysts was clearly demonstrated in the present work. The roles of both the sulfide and urea moieties of the catalyst were clarified based on the results of experimental and theoretical investigation.
尽管已经开发出了各种各样的手性有机催化剂用于不对称转化,但尽管二烷基硫催化剂具有潜在的用途,但有效的手性二烷基硫有机催化剂仍然相对较少且发展不足。在此,我们报告了具有脲部分的手性双功能二烷基硫催化剂的发展,该催化剂可用于区域、非对映和对映选择性溴内酯化。本工作清楚地证明了手性硫化物催化剂的双功能设计的重要性。根据实验和理论研究的结果,阐明了催化剂中硫化物和脲部分的作用。