Nicolai, StefanoWaser, Jerome2022-08-152022-08-152022-08-152022-07-2810.1002/anie.202209006https://infoscience.epfl.ch/handle/20.500.14299/189970WOS:000831334700001Azepanes are important seven-membered heterocycles, which are present in numerous natural and synthetic compounds. However, the development of convergent synthetic methods to access them remains challenging. Herein, we report the Lewis acid catalyzed (4+3) annulative addition of aryl and amino donor-acceptor cyclopropanes with 2-aza-1,3-dienes. Densely substituted azepane derivatives were obtained in good to excellent yields and with high diastereoselectivity. The reaction occurred under mild conditions with ytterbium triflate as the catalyst. The use of copper triflate with a trisoxazoline (Tox) ligand led to an enantioselective transformation. The obtained cycloadducts were convenient substrates for a series of further modifications, showing the synthetic utility of these compounds.Chemistry, MultidisciplinaryChemistryazadienesazepanonescycloadditionscyclopropanestox-ligandsdiels-alder reactionsdiastereoselective synthesiscycloadditionaldehydesstrategy2-aza-1,3-dienesdecarboxylationpyrrolidinesazepineindolestext::journal::journal article::research article