A facile route to cyclic and acyclic alkyl-arginines

Article abstract of DOI:10.1080/00397919808005947

Treatment of commercially available alkyl and cycloalkyl thioureas with methyl iodide provides the corresponding S-alkylisothiouronium iodide which reacts directly with ornithine to yield the title compounds.

Full text of DOI:10.1080/00397919808005947

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Synthetic Communications: An
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A Facile Route to Cyclic and
Acyclic Alkyl-Arginines
Kevin J. Kennedy a , Tiberiu L. Simandan a & Thomas
A. Dix a
a Department of Pharmaceutical Sciences , Medical
University of South Carolina , Charleston, South
Carolina, 29425
Published online: 02 Sep 2006.
To cite this article: Kevin J. Kennedy , Tiberiu L. Simandan & Thomas A. Dix (1998)
A Facile Route to Cyclic and Acyclic Alkyl-Arginines, Synthetic Communications: An
International Journal for Rapid Communication of Synthetic Organic Chemistry, 28:4,
741-746, DOI: 10.1080/00397919808005947
To link to this article: http://dx.doi.org/10.1080/00397919808005947
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