Institut de Chimie Moléculaire et des Matériaux d'Orsay (ICMMO), CNRS UMR 8182, Université Paris-Sud, Université Paris-Saclay, Bâtiment 420, 91405, Orsay, France.
Univ Rennes, CNRS UMR 6226, ISCR (Institut des Sciences Chimiques de Rennes), 35000, Rennes, France.
Angew Chem Int Ed Engl. 2020 Jan 13;59(3):1134-1138. doi: 10.1002/anie.201911761. Epub 2019 Nov 27.
Herein, we report the preparation of bridged tetrahydrobenzo[b]azepines, which was accomplished through an aza-Piancatelli cyclization/Michael addition sequence in a one-pot fashion from readily available precursors. It is noteworthy that a general method to access these scaffolds was hitherto unprecedented. Additionally, the multifaceted aspects of this process have been exemplified through its application to the synthesis of 2-azabicyclo[3.2.1]octanes and bridged tetrahydrobenzo[b]oxepines, along with post-derivatizations.
在此,我们报告了桥连四氢苯并[b]氮杂卓的制备,该方法通过一锅法的aza-Piancatelli 环化/Michael 加成序列从易得的前体中完成。值得注意的是,以前还没有一种通用的方法可以获得这些支架。此外,该方法还通过应用于 2-氮杂双环[3.2.1]辛烷和桥连四氢苯并[b]氧杂卓的合成以及后续衍生化,展示了该过程的多方面性。