Intermolecular radical carboaminohydroxylation of olefins with aryl diazonium salts and TEMPO

106Citations
Citations of this article
39Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Highly reactive aryl radicals can selectively be reacted with a broad variety of activated and nonactivated olefinic substrates in the presence of nitroxyl radicals. Direct recombination of the aryl radical and the nitroxide as well as telomerization of the olefin is successfully suppressed by the reaction conditions. © 2007 American Chemical Society.

Cite

CITATION STYLE

APA

Heinrich, M. R., Wetzel, A., & Kirschstein, M. (2007). Intermolecular radical carboaminohydroxylation of olefins with aryl diazonium salts and TEMPO. Organic Letters, 9(19), 3833–3835. https://doi.org/10.1021/ol701622d

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