Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5281932 | Tetrahedron Letters | 2008 | 4 Pages |
Abstract
This study reports a facile method for the synthesis of a variety of 5- and 6-substituted tryptophan derivatives that are difficult to prepare using alternative enzymatic approaches. Acylation of an activated amino acid, derived from serine in situ, is coupled with an enzymatic resolution step to furnish enantiopure analogues bearing a range of electron withdrawing and releasing substituents. Isolation of a dehydroalanine derivative as a by-product from some reactions provides some insights into the likely mechanism of the reaction.
Graphical abstractTryptophan derivatives can be easily synthesised from a wide range of indoles.Figure optionsDownload full-size imageDownload as PowerPoint slide
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