A new strategy for the synthesis of four individual isomers of β-methylphenylalanine

Article abstract of DOI:10.1080/00397919508010789

The application of an allylic strain effect in boron enolates and asymmetric Michael-like addition/electrophilic bromination reactions is reported for the asymmetric synthesis of the individual isomers of unusual constrained amino acids. For β-substituted

Full text of DOI:10.1080/00397919508010789

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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A New Strategy for
the Synthesis of Four
Individual Isomers of β-
Methylphenylalanine
Feng-Di Lung a , Guigen Li a , Bith-Show Lou a
Victor J. Hruby a
&
a Department of Chemistry, University of Arizona,
Tucson, AZ, 85721
Published online: 23 Sep 2006.
To cite this article: Feng-Di Lung , Guigen Li , Bith-Show Lou & Victor J.
Hruby (1995): A New Strategy for the Synthesis of Four Individual Isomers of β-
Methylphenylalanine, Synthetic Communications: An International Journal for Rapid
Communication of Synthetic Organic Chemistry, 25:1, 57-61
To link to this article: http://dx.doi.org/10.1080/00397919508010789
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