| Literature DB >> 31141295 |
Mani Sengoden1, Michael North1, Adrian C Whitwood1.
Abstract
Oxazolidinone synthesis through the coupling of carbon dioxide and aziridines was catalysed by an aluminium(salphen) complex at 50-100 °C and 1-10 bar pressure under solvent-free conditions. The process was applicable to a variety of substituted aziridines, giving products with high regioselectivity. It involved the use of a sustainable and reusable aluminium-based catalyst, used carbon dioxide as a C1 source and provided access to pharmaceutically important oxazolidinones as illustrated by a total synthesis of toloxatone. This protocol was scalable, and the catalyst could be recovered and reused. A catalytic cycle was proposed based on stereochemical, kinetic and Hammett studies.Entities:
Keywords: Schiff bases; aluminium catalysis; aziridines; carbon dioxide fixation; oxazolidinones
Year: 2019 PMID: 31141295 DOI: 10.1002/cssc.201901171
Source DB: PubMed Journal: ChemSusChem ISSN: 1864-5631 Impact factor: 8.928