An Aluminum Fluoride Complex with an Appended Ammonium Salt as an Exceptionally Active Cooperative Catalyst for the Asymmetric Carboxycyanation of Aldehydes

التفاصيل البيبلوغرافية
العنوان: An Aluminum Fluoride Complex with an Appended Ammonium Salt as an Exceptionally Active Cooperative Catalyst for the Asymmetric Carboxycyanation of Aldehydes
المؤلفون: Daniel Brodbeck, Jan Meisner, Delphine Garnier, Florian Broghammer, Julian Klepp, Johannes Kästner, René Peters, Wolfgang Frey
المصدر: Angewandte Chemie International Edition. 56:4056-4060
بيانات النشر: Wiley, 2017.
سنة النشر: 2017
مصطلحات موضوعية: chemistry.chemical_classification, Aluminum fluoride, 010405 organic chemistry, Chemistry, Enantioselective synthesis, Salt (chemistry), General Chemistry, 010402 general chemistry, 01 natural sciences, Catalysis, 0104 chemical sciences, chemistry.chemical_compound, Polymer chemistry, Organic chemistry, Ammonium, Bond energy
الوصف: Al−F bonds are among the most stable σ bonds known, exhibiting an even higher bond energy than Si−F bonds. Despite a stability advantage and a potentially high Lewis acidity of Al−F complexes, they have not been described as structurally defined catalysts for enantioselective reactions. We show that Al−F salen complexes with appended ammonium moieties give exceptional catalytic activity in asymmetric carboxycyanations. In addition to aromatic aldehydes, enal and aliphatic substrates are well accepted. Turnover numbers up to around 104 were achieved, whereas with previous catalysts 101–102 turnovers were typically attained. In contrast to Al−Me and Al−Cl salen complexes, the analogous Al−F species are remarkably stable towards air, water, and heat, and can be recovered unchanged after catalysis. They possess a considerably increased Lewis acidity as shown by DFT calculations.
تدمد: 1433-7851
DOI: 10.1002/anie.201612493
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7cb70897cc54dc44646e4620babe569a
https://doi.org/10.1002/anie.201612493
Rights: CLOSED
رقم الانضمام: edsair.doi.dedup.....7cb70897cc54dc44646e4620babe569a
قاعدة البيانات: OpenAIRE
الوصف
تدمد:14337851
DOI:10.1002/anie.201612493