A short stereoselective synthesis of a cyclopropyl analog of γ- aminobutyric acid (GABA)

Article abstract of DOI:10.1080/00397919908085899

An efficient synthesis of (S,S)-2-(aminomethyl) cyclopropane carboxylic acid has been achieved in 7 steps (38% overall yield) starting from commercially available cinnamyl alcohol. The synthesis involves initial stereoselective formation of the functional

Full text of DOI:10.1080/00397919908085899

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Synthetic Communications: An
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A Short Stereoselective Synthesis
of a Cyclopropyl Analog of γ-
Aminobutyric acid (GABA)
Debendra K. Mohapatra a
a Organic III, Indian Institute of Chemical Technology ,
Hyderabad, 500 007, India
Published online: 17 Sep 2007.
To cite this article: Debendra K. Mohapatra (1999) A Short Stereoselective Synthesis
of a Cyclopropyl Analog of γ-Aminobutyric acid (GABA), Synthetic Communications: An
International Journal for Rapid Communication of Synthetic Organic Chemistry, 29:23,
4261-4268
To link to this article: http://dx.doi.org/10.1080/00397919908085899
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