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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 40, 2010 - Issue 19
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Original Articles

Aqueous Aza-Michael Reaction of Conjugated Alkenes: Toward Spermine

, &
Pages 2857-2863 | Received 15 Jun 2009, Published online: 25 Aug 2010
 

Abstract

An aqueous aza-Michael reaction is efficiently achieved with excellent conversions without any additives. The method works very well on a molar scale with selectively for aliphatic amines. An intermediate for spermine is also made by this green process.

ACKNOWLEDGMENTS

We are grateful to Gujarat Narmada Fertilizer Corporation (Bharuch) for the financial support and to Prof. B. V. Kamath for his constant encouragement as well as providing laboratory facilities.

Notes

Notes. A, with acrylonitrile; B, with tert-butyl acrylate.

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