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Enantioselective Amination of 4‑Substituted Pyrazolones Cat..:

Rodrigo Sánchez-Molpeceres ; Laura Martín ; Noelia Esteban...
doi:10.1021/acs.joc.3c02069.s001. , 2023

Link: https://doi.org/10.1021/acs.joc.3c02069.s001

RT Journal
T1 <Title>Enantioselective Amination of 4‑Substituted Pyrazolones Catalyzed by Oxindole-Containing Thioureas and by a Recyclable Linear-Polymer-Supported Analogue in a Continuous Flow Process</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftunivoxfordfig:oai:figshare.com:article_24809484&Exemplar=1&LAN=DE
				
A1 Rodrigo Sánchez-Molpeceres
A1 Laura Martín
A1 Noelia Esteban
A1 Jesús A. Miguel
A1 Alicia Maestro
A1 José M. Andrés
YR 2023
K1 Biophysics
K1 Biochemistry
K1 Molecular Biology
K1 Biotechnology
K1 Evolutionary Biology
K1 Mental Health
K1 Infectious Diseases
K1 Plant Biology
K1 Virology
K1 Biological Sciences not elsewhere classified
K1 Chemical Sciences not elsewhere classified
K1 Physical Sciences not elsewhere classified
K1 efficient heterogeneous organocatalyst
K1 bifunctional aromatic monomer
K1 short reaction times
K1 supported bifunctional thiourea
K1 continuous flow process
K1 supported analogue
K1 flow processes
K1 derived thiourea
K1 amination reaction
K1 superacidic media
K1 room temperature
K1 recycling experiments
K1 pyrazolone derivatives
K1 practical value
K1 novel quinine
K1 immobilized catalyst
K1 high yields
K1 high yield
K1 gram scale
K1 excellent enantioselectivities
K1 enantioselective amination
K1 containing thioureas
K1 azodicarboxylates mediated
JF doi:10.1021/acs.joc.3c02069.s001
LK http://dx.doi.org/https://doi.org/10.1021/acs.joc.3c02069.s001
DO https://doi.org/10.1021/acs.joc.3c02069.s001
SF ELIB - SuUB Bremen

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