Journal Article

Oxidative Intramolecular 1,2-Amino-Oxygenation of Alkynes under AuI/AuIIICatalysis: Discovery of a Pyridinium-Oxazole Dyad as an Ionic Fluorophore

Angewandte Chemie - International Edition (2017) 56(3) 757-761
DOI: 10.1002/anie.201609335
62Citations
Citations of this article
32Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Oxidative intramolecular 1,2-amino-oxygenation reactions, combining gold(I)/gold(III) catalysis, is reported. The reaction provides efficient access to a structurally unique ionic pyridinium-oxazole dyad with tunable emission wavelengths. The application of these fluorophores as potential biomarkers has been investigated.

Author supplied keywords

Cite

CITATION STYLE

APA

Shaikh, A. C., Ranade, D. S., Rajamohanan, P. R., Kulkarni, P. P., & Patil, N. T. (2017). Oxidative Intramolecular 1,2-Amino-Oxygenation of Alkynes under AuI/AuIIICatalysis: Discovery of a Pyridinium-Oxazole Dyad as an Ionic Fluorophore. Angewandte Chemie - International Edition, 56(3), 757–761. https://doi.org/10.1002/anie.201609335

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free