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Enantioselective organocatalytic amination of pyrazolones

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
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), 64-68. (doi:10.1002/ajoc.201200168).

Record type: Article

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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More information

Published date: 2013
Organisations: Organic Chemistry: Synthesis, Catalysis and Flow, Chemistry, Faculty of Natural and Environmental Sciences

Identifiers

Local EPrints ID: 348581
URI: http://eprints.soton.ac.uk/id/eprint/348581
PURE UUID: a8310a52-7f15-411b-9624-e678e451e8de
ORCID for Ramon Rios: ORCID iD orcid.org/0000-0002-3843-8521

Catalogue record

Date deposited: 14 Feb 2013 13:52
Last modified: 15 Sep 2021 01:59

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