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Chiral azo compounds: enantioselective synthesis and transformations into beta-amino alcohols and alpha-amino acids with a quaternary stereocenter
Journal article   Peer reviewed

Chiral azo compounds: enantioselective synthesis and transformations into beta-amino alcohols and alpha-amino acids with a quaternary stereocenter

Friedrich R. Dietz, Agnes Prechter, Harald Groeger and Markus R. Heinrich
Tetrahedron letters, Vol.52(6), pp.655-657
09/02/2011
DOI: https://doi.org/10.1016/j.tetlet.2010.11.137

Abstract

Chemistry Chemistry, Organic Physical Sciences Science & Technology
Taking advantage of radical carboaminations producing azo compounds, a new chemo-enzymatic approach to enantiomerically enriched azo alcohols, beta-amino alcohols and non-natural (aromatic) amino acids with a quaternary stereocenter is reported. (C) 2010 Elsevier Ltd. All rights reserved.

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