Organocatalytic racemization of alpha-aryl propionates in the presence of water

Alfaro Blasco M, Gröger H (2012)
Synth. Commun. 43(1): 9-15.

Journal Article | Published | English

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Abstract
An organocatalytic method for the racemization of alpha-aryl propionates, which proceeds even in the presence of an aqueous phase, has been developed, thus fulfilling a prerequisite for a dynamic kinetic resolution of corresponding esters with hydrolase as a biocatalyst. The desired racemization of ethyl 2-phenylpropionate and 2-ibuprofen ethyl ester as substrates has been achieved in a two-phase system. As preferred organocatalysts for the racemization, 1,8-diazabicyclo[5.4.0] undec-7-ene and 1,5,7-triazabicyclo[4.4.0] dec-5-ene (TBD) have been used.
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Alfaro Blasco M, Gröger H. Organocatalytic racemization of alpha-aryl propionates in the presence of water. Synth. Commun. 2012;43(1):9-15.
Alfaro Blasco, M., & Gröger, H. (2012). Organocatalytic racemization of alpha-aryl propionates in the presence of water. Synth. Commun., 43(1), 9-15.
Alfaro Blasco, M., and Gröger, H. (2012). Organocatalytic racemization of alpha-aryl propionates in the presence of water. Synth. Commun. 43, 9-15.
Alfaro Blasco, M., & Gröger, H., 2012. Organocatalytic racemization of alpha-aryl propionates in the presence of water. Synth. Commun., 43(1), p 9-15.
M. Alfaro Blasco and H. Gröger, “Organocatalytic racemization of alpha-aryl propionates in the presence of water”, Synth. Commun., vol. 43, 2012, pp. 9-15.
Alfaro Blasco, M., Gröger, H.: Organocatalytic racemization of alpha-aryl propionates in the presence of water. Synth. Commun. 43, 9-15 (2012).
Alfaro Blasco, M., and Gröger, Harald. “Organocatalytic racemization of alpha-aryl propionates in the presence of water”. Synth. Commun. 43.1 (2012): 9-15.
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