Sulwey Dennis, DiSapio Julia B, Gascón José A, Howell Amy R
Department of Chemistry, University of Connecticut, Storrs, Connecticut 06269-3060, United States.
J Org Chem. 2024 Nov 15;89(22):16571-16585. doi: 10.1021/acs.joc.4c01877. Epub 2024 Nov 5.
The first general synthesis of 2-halomethyleneoxetanes, realized by the reaction of 2-methyleneoxetanes with -halosuccinimides (NXS), is reported. The relative diastereoselectivities of the transformations were dependent on the halogen of NXS, while alternative reaction outcomes were influenced by substituents on the oxetane. Quantum mechanical calculations and molecular dynamics simulations exploring the basis of the observed diastereoselectivities are described. These highly strained heterocycles underwent standard cross-coupling reactions, demonstrating their utility as synthetic intermediates.
报道了通过2-亚甲基氧杂环丁烷与卤代琥珀酰亚胺(NXS)反应实现的2-卤亚甲基氧杂环丁烷的首次通用合成。转化反应的相对非对映选择性取决于NXS的卤素,而其他反应结果则受氧杂环丁烷上取代基的影响。描述了探索所观察到的非对映选择性基础的量子力学计算和分子动力学模拟。这些高度张力的杂环进行了标准的交叉偶联反应,证明了它们作为合成中间体的实用性。