We found a match
Your institution may have access to this item. Find your institution then sign in to continue.
- Title
Biocatalytic Asymmetric Synthesis of Optically Pure Aromatic Propargylic Amines Employing ω-Transaminases.
- Authors
Schmidt, Nina G.; Simon, Robert C.; Kroutil, Wolfgang
- Abstract
The asymmetric reductive bio-amination of prochiral aromatic propargyl ketones led to the corresponding amines in optically pure form ( ee>99%). The ( R)- as well as the ( S)-enantiomers of the propargylic amines were obtained, employing either ( R)-selective ω-transaminases (ω-TAs) originating from Arthrobacter sp. and Aspergillus terreus or an ( S)-selective ω-TA from Chromobacterium violaceum. The product propargylic amines were obtained with high conversions (up to 99%). To simplify product isolation, protection of the free amino group to the corresponding acetamides or benzamides was performed without loss of optical puritiy. The final products were isolated in moderate to good yields (33-67% over two steps) in optical pure form without additional purification steps. Although propargyl ketones are described in the literature to be irreversible inhibitors for aminotransferases, suitable ω-transaminases were identified for the amination of these compounds.
- Subjects
AMINOTRANSFERASES; BIOCATALYSIS; AMINES; PROPARGYL alcohol; KETONES
- Publication
Advanced Synthesis & Catalysis, 2015, Vol 357, Issue 8, p1815
- ISSN
1615-4150
- Publication type
Article
- DOI
10.1002/adsc.201500086