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

Dietz FR, Prechter A, Gröger H, Heinrich MR (2011)
TETRAHEDRON LETTERS 52(6): 655-657.

Journal Article | Published | English

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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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Dietz FR, Prechter A, Gröger H, Heinrich MR. Chiral azo compounds: enantioselective synthesis and transformations into beta-amino alcohols and alpha-amino acids with a quaternary stereocenter. TETRAHEDRON LETTERS. 2011;52(6):655-657.
Dietz, F. R., Prechter, A., Gröger, H., & Heinrich, M. R. (2011). Chiral azo compounds: enantioselective synthesis and transformations into beta-amino alcohols and alpha-amino acids with a quaternary stereocenter. TETRAHEDRON LETTERS, 52(6), 655-657.
Dietz, F. R., Prechter, A., Gröger, H., and Heinrich, M. R. (2011). Chiral azo compounds: enantioselective synthesis and transformations into beta-amino alcohols and alpha-amino acids with a quaternary stereocenter. TETRAHEDRON LETTERS 52, 655-657.
Dietz, F.R., et al., 2011. Chiral azo compounds: enantioselective synthesis and transformations into beta-amino alcohols and alpha-amino acids with a quaternary stereocenter. TETRAHEDRON LETTERS, 52(6), p 655-657.
F.R. Dietz, et al., “Chiral azo compounds: enantioselective synthesis and transformations into beta-amino alcohols and alpha-amino acids with a quaternary stereocenter”, TETRAHEDRON LETTERS, vol. 52, 2011, pp. 655-657.
Dietz, F.R., Prechter, A., Gröger, H., Heinrich, M.R.: Chiral azo compounds: enantioselective synthesis and transformations into beta-amino alcohols and alpha-amino acids with a quaternary stereocenter. TETRAHEDRON LETTERS. 52, 655-657 (2011).
Dietz, Friedrich R., Prechter, Agnes, Gröger, Harald, and Heinrich, Markus R. “Chiral azo compounds: enantioselective synthesis and transformations into beta-amino alcohols and alpha-amino acids with a quaternary stereocenter”. TETRAHEDRON LETTERS 52.6 (2011): 655-657.
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