Issue 19, 2018

Solvent-free N-iodosuccinimide-promoted synthesis of spiroimidazolines from alkenes and amidines under ball-milling conditions

Abstract

A novel N-iodosuccinimide-promoted intermolecular cyclization between alkenes and amidines has been demonstrated under solvent-free ball-milling conditions, affording a variety of spiroimidazolines with remarkable functional group tolerance and good to excellent yields. The present protocol features short reaction time, mild reaction conditions, high atom economy and feasibility of large-scale synthesis, providing an efficient and environmentally friendly access to spiroimidazolines.

Graphical abstract: Solvent-free N-iodosuccinimide-promoted synthesis of spiroimidazolines from alkenes and amidines under ball-milling conditions

Supplementary files

Article information

Article type
Research Article
Submitted
16 Jul 2018
Accepted
02 Sep 2018
First published
03 Sep 2018

Org. Chem. Front., 2018,5, 2864-2869

Solvent-free N-iodosuccinimide-promoted synthesis of spiroimidazolines from alkenes and amidines under ball-milling conditions

H. Xu, K. Chen, H. Liu and G. Wang, Org. Chem. Front., 2018, 5, 2864 DOI: 10.1039/C8QO00723C

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