Issue 75, 2014

Transition metal and base free synthesis of 2-aryl-2-oxazolines from aldehydes and β-amino alcohols catalysed by potassium iodide

Abstract

Synthesis of 2-aryl-2-oxazolines from β-amino alcohols and aldehydes was achieved in good to excellent yield by employing a potassium iodide (KI)–tert-butyl hydroperoxide (TBHP) catalytic system. This protocol is very mild, metal and base free and can be performed under ambient reaction conditions. This oxidative cyclization strategy was further extended for the synthesis of optically active 2-oxazolines, which can act as very useful chiral auxiliaries and as ligands.

Graphical abstract: Transition metal and base free synthesis of 2-aryl-2-oxazolines from aldehydes and β-amino alcohols catalysed by potassium iodide

Supplementary files

Article information

Article type
Communication
Submitted
08 Jul 2014
Accepted
21 Aug 2014
First published
21 Aug 2014

RSC Adv., 2014,4, 39897-39900

Author version available

Transition metal and base free synthesis of 2-aryl-2-oxazolines from aldehydes and β-amino alcohols catalysed by potassium iodide

C. Uma Maheswari, G. Sathish Kumar and M. Venkateshwar, RSC Adv., 2014, 4, 39897 DOI: 10.1039/C4RA08578G

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