Darses Benjamin, Maldivi Pascale, Philouze Christian, Dauban Philippe, Poisson Jean-François
Univ. Grenoble Alpes, CNRS, DCM, 38000 Grenoble, France.
Institut de Chimie des Substances Naturelles, CNRS UPR-2301, Université Paris-Sud, Université Paris-Saclay, 1 av. de la Terrasse, 91198 Gif-sur-Yvette, France.
Org Lett. 2021 Jan 15;23(2):300-304. doi: 10.1021/acs.orglett.0c03774. Epub 2021 Jan 4.
Bicyclic compounds bearing a quaternary stereogenic center have been obtained using asymmetric intramolecular Buchner reaction with excellent yields and level of enantioselectivity. X-ray crystallography determination of the absolute configuration of one product has led to the serendipitous observation of an unusual behavior within the crystal structure, with equilibrating norcaradiene and cycloheptatriene valence isomers at the solid state, as well as an even more unexpected intermediate form. DFT calculations were performed to support these observations.
通过不对称分子内布赫纳反应,已获得带有季立体中心的双环化合物,产率和对映选择性水平都很高。对一种产物的绝对构型进行X射线晶体学测定时,意外发现了晶体结构中的一种异常行为,即降蒈二烯和环庚三烯价异构体在固态下相互平衡,还有一种更意想不到的中间形式。进行了密度泛函理论计算以支持这些观察结果。