A convenient preparation of farnesylamine

Article abstract of DOI:10.1080/00397919308009810

The efficient synthesis of farnesylamine (1) was accomplished by two separate routes. The first, by the alkylation of trifluoroacetamide with farnesyl bromide followed by base hydrolysis. The second, by displacement of the halogen of farnesyl bromide with lithium bis(trimethylsilyl)amide followed by methanolysis.

Full text of DOI:10.1080/00397919308009810

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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A Convenient Preparation of
Farnesylamine
Gary M. Coppola a & Mahavir Prashad a
a Sandoz Research Institute Chemistry Research
Department Sandoz , Inc. Route 10, East Hanover,
New Jersey, 07936
Published online: 23 Sep 2006.
To cite this article: Gary M. Coppola & Mahavir Prashad (1993) A Convenient
Preparation of Farnesylamine, Synthetic Communications: An International Journal
for Rapid Communication of Synthetic Organic Chemistry, 23:4, 535-541, DOI:
10.1080/00397919308009810
To link to this article: http://dx.doi.org/10.1080/00397919308009810
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