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|Title: ||An alkylation route to carbo- and heteroaromatic amino acids|
|Authors: ||Jones, Raymond C.F.|
Berthelot, Didier J.C.
Iley, James N.
|Keywords: ||Amino acid|
|Issue Date: ||2007|
|Publisher: ||© ARKAT USA, Inc.|
|Citation: ||JONES, R.C.F., BERTHELOT, D.J.C. and ILEY, J.N., 2007. An alkylation route to carbo- and heteroaromatic amino acids. ARKIVOC, 2007 (xi), pp. 73-84|
|Abstract: ||Amino acids carrying aromatic carbo- and heterocycles in the side chain, such as naphthyl-,
biphenyl- and pyridylalanines, have been prepared by alkylation of a glycine enolate with a
haloalkyl carbocycle or heterocycle, with enantiomeric excess up to 87% using the ephedrine
|Description: ||This is an article that was published in the journal, ARKIVOC [© ARKAT USA]. It is also available at; http://www.arkat-usa.org/arkivoc-journal/browse-arkivoc/|
|Appears in Collections:||Published Articles (Chemistry)|
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