Literature DB >> 31141295

Synthesis of Oxazolidinones by using Carbon Dioxide as a C1 Building Block and an Aluminium-Based Catalyst.

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.
© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

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


  2 in total

Review 1.  Recent Advances in the Chemistry of Metal Carbamates.

Authors:  Giulio Bresciani; Lorenzo Biancalana; Guido Pampaloni; Fabio Marchetti
Journal:  Molecules       Date:  2020-08-07       Impact factor: 4.411

2.  Ring-opening of non-activated aziridines with [11C]CO2 via novel ionic liquids.

Authors:  Anton Lindberg; Neil Vasdev
Journal:  RSC Adv       Date:  2022-08-02       Impact factor: 4.036

  2 in total

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