2024-03-28T12:41:46Zhttp://uvadoc.uva.es/oai/requestoai:uvadoc.uva.es:10324/214532021-06-23T11:57:34Zcom_10324_1187com_10324_931com_10324_894col_10324_1409
2016-12-05T14:12:13Z
urn:hdl:10324/21453
Prolinamides as Asymmetric Organocatalysts
Pedrosa Sáez, Rafael
Andrés García, José María
Química orgánica
Producción Científica
Prolinamides are valuable organocatalysts for enantioselective transformations that occur by activation of the nucleophile by enamine formation. Different substituents can be appended on the nitrogen atom of the carboxamide, which allow for the modulation of the catalytic properties. In that way, the acidity, the hydrogen donor properties, the hydrophobicity, or the chiral environment can be modified, in a few steps, starting from easily available proline.
2016-12-05T14:12:13Z
2016-12-05T14:12:13Z
2015
info:eu-repo/semantics/bookPart
Sustainable Catalysis: Without Metals or Other Endangered Elements, Part 1. Editor, Michael North. 2015, Chapter 6, p.120-139
978-1-78262-209-3
http://uvadoc.uva.es/handle/10324/21453
120
139
Sustainable Catalysis: Without Metals or Other Endangered Elements
eng
http://pubs.rsc.org/
info:eu-repo/semantics/restrictedAccess
http://creativecommons.org/licenses/by-nc-nd/4.0/
© The Royal Society of Chemistry
Attribution-NonCommercial-NoDerivatives 4.0 International
Royal Society of Chemistry