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Author Notes:

Department of Chemistry, Winship Cancer Institute, Emory University, Atlanta, USA E-mail: njui@emory.edu

We gratefully acknowledge Prof. Huw Davies for generous access to instrumentation and chemicals.

Subjects:

Research Funding:

Financial support was provided by Emory University and Winship Cancer Institute.

A mild catalytic system for radical conjugate addition of nitrogen heterocycles

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Journal Title:

Chemical Science

Volume:

Volume 8, Number 4

Publisher:

, Pages 3121-3125

Type of Work:

Article | Final Publisher PDF

Abstract:

The direct addition of pyridine and diazine units to electron-poor alkenes has been achieved via a redox radical mechanism that is enabled by limiting the effective concentration of the hydrogen-atom source. The described method is tolerant of acidic functional groups and is generally applicable to the union of a wide range of Michael acceptors and 6-membered heterocyclic halides.

Copyright information:

© The Royal Society of Chemistry 2017

This is an Open Access work distributed under the terms of the Creative Commons Attribution 3.0 Unported License (http://creativecommons.org/licenses/by/3.0/).

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