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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 16, 1986 - Issue 11
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Original Articles

The Reaction of 2-Aryl-N, N-Dimethylallylic Amines with Organolithium Reagents

John T. Gupton Department of Chemistry, University of Central Florida, Orlando, FL, 32816
,
William J. Layman Department of Chemistry, University of Central Florida, Orlando, FL, 32816
&
James T. Forman Department of Chemistry, University of Central Florida, Orlando, FL, 32816
Pages 1393-1399 | Published online: 05 Dec 2006

Citations (4)

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Read on this site (1)

JohnT. Gupton, John Dicesare, Joan Brown & JohnP. Idoux. (1989) The Reaction of Quaternary Ammonium Salts Derived from 2-Aryl-3-(N,N-dimethylamino)-1-propenes with Oxygen Containing Nucleophiles. Synthetic Communications 19:7-8, pages 1413-1422.
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Articles from other publishers (3)

Manfred Schlosser. 2013. Organometallics in Synthesis. Organometallics in Synthesis 1 222 .
Zhen Jiang, Lingjuan Zhang, Chaonan Dong, Baode Ma, Weijun Tang, Lijin Xu, Qinghua Fan & Jianliang Xiao. (2012) Palladium-catalyzed highly regioselective and stereoselective arylation of electron-rich allylamines with aryl bromides. Tetrahedron 68:24, pages 4919-4926.
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J. T. GUPTON, W. J. LAYMAN & J. T. FORMAN. (2016) ChemInform Abstract: The Reaction of 2‐Aryl‐N,N‐dimethylallylic Amines with Organolithium Reagents.. ChemInform 18:10.
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