Enantioselective organocatalytic amination of pyrazolones
Enantioselective organocatalytic amination of pyrazolones
Easy as py: The organocatalytic enantioselective amination of pyrazolones is reported. The reaction between pyrazolones and diazodicarboxylates is simple and is catalyzed by quinine to afford the final aminopyarazolone derivatives in excellent yields and good enantioselectivity.
64-68
Šimek, Michal
60be1d2e-ee0d-4226-80b9-21989ad23b72
Remeš, Marek
e138962c-f082-4705-96d9-2396e06e72b7
Veselý, Jan
9d4ecc53-859e-451a-a018-636d416bb3fe
Rios, Ramon
609bedf2-e886-4d62-a676-a32b6f8c1441
2013
Šimek, Michal
60be1d2e-ee0d-4226-80b9-21989ad23b72
Remeš, Marek
e138962c-f082-4705-96d9-2396e06e72b7
Veselý, Jan
9d4ecc53-859e-451a-a018-636d416bb3fe
Rios, Ramon
609bedf2-e886-4d62-a676-a32b6f8c1441
Šimek, Michal, Remeš, Marek, Veselý, Jan and Rios, Ramon
(2013)
Enantioselective organocatalytic amination of pyrazolones.
Asian Journal of Organic Chemistry, 2 (1), .
(doi:10.1002/ajoc.201200168).
Abstract
Easy as py: The organocatalytic enantioselective amination of pyrazolones is reported. The reaction between pyrazolones and diazodicarboxylates is simple and is catalyzed by quinine to afford the final aminopyarazolone derivatives in excellent yields and good enantioselectivity.
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Published date: 2013
Organisations:
Organic Chemistry: Synthesis, Catalysis and Flow, Chemistry, Faculty of Natural and Environmental Sciences
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Local EPrints ID: 348581
URI: http://eprints.soton.ac.uk/id/eprint/348581
PURE UUID: a8310a52-7f15-411b-9624-e678e451e8de
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Date deposited: 14 Feb 2013 13:52
Last modified: 14 Mar 2024 13:02
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Contributors
Author:
Michal Šimek
Author:
Marek Remeš
Author:
Jan Veselý
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