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Stereoselective Amine Synthesis Mediated by a Zirconocene H..:

Athenea N. Aloiau ; Briana M. Bobek ; Kersti Caddell Haatveit...
https://figshare.com/articles/journal_contribution/Stereoselective_Amine_Synthesis_Mediated_by_a_Zirconocene_Hydride_to_Accelerate_a_Drug_Discovery_Program/25321026. , 1753

Link: https://doi.org/10.1021/acs.joc.3c02723.s001

RT Journal
T1 <Title>Stereoselective Amine Synthesis Mediated by a Zirconocene Hydride to Accelerate a Drug Discovery Program</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonianinsp:oai:figshare.com:article_25321026&Exemplar=1&LAN=DE
				
A1 Athenea N. Aloiau
A1 Briana M. Bobek
A1 Kersti Caddell Haatveit
A1 Kelly E. Pearson
A1 Ashlee H. Watkins
A1 Benjamin Jones
A1 Christopher R. Smith
A1 John M. Ketcham
A1 Matthew A. Marx
A1 Stephen J. Harwood
YR 1753
K1 Biochemistry
K1 Medicine
K1 Genetics
K1 Molecular Biology
K1 Neuroscience
K1 Physiology
K1 Pharmacology
K1 Virology
K1 Biological Sciences not elsewhere classified
K1 Chemical Sciences not elsewhere classified
K1 mediated reduction helped
K1 gave highly chemo
K1 drug discovery programs
K1 drug discovery efforts
K1 computational investigation supported
K1 chair transition state
K1 zirconium hydride
K1 sulfinyl ketimines
K1 stereoselective reductions
K1 significant challenge
K1 medicinal chemistry
K1 lower reactivity
K1 high selectivity
K1 high oxophilicity
K1 design cycle
K1 cyclic half
K1 benzyl systems
JF https://figshare.com/articles/journal_contribution/Stereoselective_Amine_Synthesis_Mediated_by_a_Zirconocene_Hydride_to_Accelerate_a_Drug_Discovery_Program/25321026
LK http://dx.doi.org/https://doi.org/10.1021/acs.joc.3c02723.s001
DO https://doi.org/10.1021/acs.joc.3c02723.s001
SF ELIB - SuUB Bremen

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