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Synthesis of Stereodefined Polysubstituted Bicyclo[1.1.0]butanes
Journal of the American Chemical Society ( IF 14.4 ) Pub Date : 2024-05-09 , DOI: 10.1021/jacs.4c04438 Rahul Suresh 1 , Noam Orbach 1 , Ilan Marek 1
Journal of the American Chemical Society ( IF 14.4 ) Pub Date : 2024-05-09 , DOI: 10.1021/jacs.4c04438 Rahul Suresh 1 , Noam Orbach 1 , Ilan Marek 1
Affiliation
We report a highly diastereoselective synthesis of polysubstituted bicyclobutanes possessing up to three stereodefined quaternary centers and five substituents. Our strategy involves a diastereoselective carbometalation of cyclopropenes followed by a cyclization to furnish the bicyclobutane ring system. This straightforward approach allows for the incorporation of a diverse range of substituents and functional groups, notably without the need for electron-withdrawing functionalities.
中文翻译:
立体多取代双环[1.1.0]丁烷的合成
我们报道了多取代双环丁烷的高度非对映选择性合成,该多取代双环丁烷具有多达三个立体定义的四级中心和五个取代基。我们的策略涉及环丙烯的非对映选择性碳金属化,然后环化以提供双环丁烷环系统。这种简单的方法允许掺入各种取代基和官能团,特别是不需要吸电子功能。
更新日期:2024-05-09
中文翻译:
立体多取代双环[1.1.0]丁烷的合成
我们报道了多取代双环丁烷的高度非对映选择性合成,该多取代双环丁烷具有多达三个立体定义的四级中心和五个取代基。我们的策略涉及环丙烯的非对映选择性碳金属化,然后环化以提供双环丁烷环系统。这种简单的方法允许掺入各种取代基和官能团,特别是不需要吸电子功能。