| Literature DB >> 26352021 |
Longrui Chen1, Mark O Bovee1, Betsegaw E Lemma2, Kimberlee S M Keithley2, Sara L Pilson2, Michael G Coleman3, James Mack4.
Abstract
The diastereoselective cyclopropanation of various alkenes with diazoacetate derivatives can be achieved under mechanochemical conditions using metallic silver foil and a stainless-steel vial and ball system. This solvent-free method displays analogous reactivity and selectivity to solution-phase reactions without the need for slow diazoacetate addition or an inert atmosphere. The heterogeneous silver-foil catalyst system is easily recyclable without any appreciable loss of activity or selectivity being observed. The cyclopropanation products were obtained with excellent diastereoselectivities (up to 98:2 d.r.) and in high yields (up to 96 %).Entities:
Keywords: cycloaddition; green chemistry; heterogeneous catalysis; solid-phase synthesis; sustainable chemistry
Year: 2015 PMID: 26352021 DOI: 10.1002/anie.201504236
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336