Issue 24, 2016

Investigation of the dynamic nature of 1,2-oxazines derived from peralkylcyclopentadiene and nitrosocarbonyl species

Abstract

We have investigated the reversible hetero-Diels–Alder reaction of 1,2-oxazines derived from a peralkylcyclopentadiene and a series of nitrosocarbonyl dienophiles. The nature of the dienophile was found to impart broad tunability to the dynamic character of the oxazine adducts. The reversibility was also observed in polymeric systems. The fidelity of the reaction and tunable sensitivity toward elevated temperature and water signify potential applications in the development of dynamic covalent materials or delivery systems for small molecule payloads.

Graphical abstract: Investigation of the dynamic nature of 1,2-oxazines derived from peralkylcyclopentadiene and nitrosocarbonyl species

  • This article is part of the themed collection: New Talent

Supplementary files

Article information

Article type
Communication
Submitted
20 Feb 2016
Accepted
26 Apr 2016
First published
26 Apr 2016

Org. Biomol. Chem., 2016,14, 5617-5621

Investigation of the dynamic nature of 1,2-oxazines derived from peralkylcyclopentadiene and nitrosocarbonyl species

V. K. Kensy, G. I. Peterson, D. C. Church, N. A. Yakelis and A. J. Boydston, Org. Biomol. Chem., 2016, 14, 5617 DOI: 10.1039/C6OB00400H

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