Engaging unactivated alkyl, alkenyl and aryl iodides in visible-light-mediated free radical reactions-Reference-Cited by-同舟云学术

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Engaging unactivated alkyl, alkenyl and aryl iodides in visible-light-mediated free radical reactions

Published:2012-09-24 Issue:10 Volume:4 Page:854-859
ISSN:1755-4330
Container-title:Nature Chemistry
language:en
Short-container-title:Nature Chem

Author:

Nguyen John D.,D'Amato Erica M.,Narayanam Jagan M. R.,Stephenson Corey R. J.

Publisher

Springer Science and Business Media LLC

Subject

General Chemical Engineering,General Chemistry

Link

http://www.nature.com/articles/nchem.1452.pdf

Reference48 articles.

1. Alonso, F., Beletskaya, I. P. & Yus, M. Metal-mediated reductive hydrodehalogenation of organic halides. Chem. Rev. 102, 4009–4091 (2002).

2. Bailey, W. F. & Patricia, J. J. The mechanism of the lithium halogen interchange reaction—a review of the literature. J. Organomet. Chem. 352, 1–46 (1988).

3. Knochel, P. et al. Highly functionalized organomagnesium reagents prepared through halogen–metal exchange. Angew. Chem. Int. Ed. 42, 4302–4320 (2003).

4. Yoon, N. M. Selective reduction of organic compounds with aluminum and boron hydrides. Pure Appl. Chem. 68, 843–848 (1996).

5. Chen, J. et al. A practical palladium catalyzed dehalogenation of aryl halides and α-haloketones. Tetrahedron 63, 4266–4270 (2007).

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