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Stereoselective Synthesis of Functionalized α-Amino Acids Isolated by Filtration
Ivan Sivák1, Michal Toběrný1, Andrea Kyselicová1
1Institute of Organic Chemistry, Catalysis and Petrochemistry , Slovak University of Technology , Radlinského 9 , Bratislava 812 37 , Slovakia.
Abstract:
Crystallization-induced diastereomer transformation (CIDT) represents a highly appealing and convenient synthetic tool. Despite its numerous advantages, it remains rather rarely used due to its uncertain predictability to occur. Herein, we describe CIDT based on aza-Michael reactions of diversely functionalized ( E)-3-acylacrylic acids. This method provides direct access to a broad variety of α-amino acid derivatives in excellent stereochemical purities.
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