[(Salcen)Cr-III + Lewis base]-catalyzed synthesis of N-aryl-substituted oxazolidinones from epoxides and aryl isocyanates

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[(Salcen)Cr-III + Lewis base] was found to be a highly active and selective catalyst system in the [2+3] cycloaddition between epoxides and isocyanates to form 5-oxazolidinones. The reaction proceeds to high yield under mild reaction conditions and is applicable to a variety of terminal epoxides and aryl isocyanates.
Publisher
ROYAL SOC CHEMISTRY
Issue Date
2014
Language
English
Article Type
Article
Keywords

CATALYZED SYNTHESIS; ISOCYANATES; CYCLOADDITION; HETEROCUMULENES; OXIRANES; 2-OXAZOLIDONES; OXAZOLIDINONES; EPOXIDES; LIGANDS; IODIDE

Citation

CHEMICAL COMMUNICATIONS, v.50, no.96, pp.15187 - 15190

ISSN
1359-7345
DOI
10.1039/c4cc07421a
URI
http://hdl.handle.net/10203/203292
Appears in Collection
CH-Journal Papers(저널논문)
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