Division of Chemistry & Biological Chemistry, School of Physical & Mathematical Sciences, Nanyang Technological University, Singapore, 637371, Singapore.
Laboratory Breeding Base of Green Pesticide and Agricultural Bioengineering, Key Laboratory of Green Pesticide and Agricultural Bioengineering, Ministry of Education, Guizhou University, Huaxi District, Guiyang, 550025, China.
Angew Chem Int Ed Engl. 2017 Apr 3;56(15):4201-4205. doi: 10.1002/anie.201700045. Epub 2017 Mar 15.
A carbene-catalyzed intermolecular C-N bond formation, which initiates a highly selective cascade reaction for the synthesis of pyrrolidine fused β-lactones, is disclosed. The nitrogen-containing bicyclic β-lactone products are obtained with good yields and excellent stereoselectivities. Synthetic transformations of the reaction products into useful functional molecules, such as amino catalysts, can be efficiently realized under mild reaction conditions. Mechanistically, this study provides insights into modulating the reactivities of heteroatoms, such as nitrogen atoms, in challenging carbene-catalyzed asymmetric carbon-heteroatom bond-forming reactions.
本文报道了一种卡宾催化的分子间 C-N 键形成反应,该反应引发了高选择性的级联反应,用于合成吡咯烷并β-内酰胺。该反应以良好的收率和优异的立体选择性得到含氮双环β-内酰胺产物。在温和的反应条件下,可以有效地将反应产物转化为有用的功能分子,如氨基催化剂。在机理上,该研究为调节氮原子等杂原子在具有挑战性的卡宾催化不对称碳-杂原子键形成反应中的反应性提供了新的见解。