| Literature DB >> 27357432 |
Vitthal B Saptal1, Bhalchandra M Bhanage2.
Abstract
In this report, the activity of N-heterocyclic olefins (NHOs) as a newly emerging class of organocatalyst is investigated for the chemical fixation of carbon dioxide through reactions with aziridines to form oxazolidinones and the N-formylation of amines with polymethylhydrosiloxane (PMHS) or 9-borabicyclo[3.3.1]nonane (9-BBN) as the reducing agent under mild conditions. The exocyclic carbon atoms of NHOs are highly nucleophilic owing to the electron-donating ability of the two nitrogen atoms. This high nucleophilicity of the NHOs activates CO2 molecules to form zwitterionic NHO-carboxylate (NHO-CO2 ) adducts, which are active in formylation reactions as well as the carboxylation of aziridines to oxazolidinones.Entities:
Keywords: carbon dioxide fixation; cycloaddition; nitrogen heterocycles; organocatalysis; zwitterions
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Year: 2016 PMID: 27357432 DOI: 10.1002/cssc.201600467
Source DB: PubMed Journal: ChemSusChem ISSN: 1864-5631 Impact factor: 8.928