| Literature DB >> 31661585 |
Shengdong Wang1, Régis Guillot1, Jean-François Carpentier2, Yann Sarazin2, Christophe Bour1, Vincent Gandon1, David Lebœuf1.
Abstract
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.Entities:
Keywords: Lewis acid; electrocyclization; hexafluoroisopropanol; medium-size N-heterocycles; tetrahydrobenzo[b]azepines
Year: 2019 PMID: 31661585 DOI: 10.1002/anie.201911761
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336