Direct formation of alkylzinc chlorides using a new active zinc

Article abstract of DOI:10.1080/00397919508010794

The reduction of zinc cyanide by lithium napthalenide yields an active form of zinc which undergoes direct oxidative addition to alkylchlorides with the tolerance of some functionality.

Full text of DOI:10.1080/00397919508010794

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Direct Formation of Alkylzevc
Chlorides Using a New Active
Zinc
a
a
Mark Hanson & Reuben D. Rieke
a
Department of Chemistry , University of Nebraska-
Lincoln , Lincoln, Nebraska, 68588-0304
Published online: 23 Sep 2006.
To cite this article: Mark Hanson & Reuben D. Rieke (1995) Direct Formation
of Alkylzevc Chlorides Using a New Active Zinc, Synthetic Communications: An
International Journal for Rapid Communication of Synthetic Organic Chemistry, 25:1,
101-104, DOI: 10.1080/00397919508010794
To link to this article: http://dx.doi.org/10.1080/00397919508010794
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