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An Asymmetric S N 2 Dynamic Kinetic Resolution:

Nomaan M. Rezayee (2611792) ; Valdemar J. Enemærke (10744883) ; Sif T. Linde (10744886)...
https://figshare.com/articles/journal_contribution/An_Asymmetric_S_sub_N_sub_2_Dynamic_Kinetic_Resolution/14535656. , 2021

Link: https://doi.org/10.1021/jacs.1c02193.s001

RT Journal
T1 <Title>An Asymmetric S N 2 Dynamic Kinetic Resolution</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonian:oai:figshare.com:article_14535656&Exemplar=1&LAN=DE
				
A1 Nomaan M. Rezayee (2611792)
A1 Valdemar J. Enemærke (10744883)
A1 Sif T. Linde (10744886)
A1 Johannes N. Lamhauge (10744889)
A1 Gabriel J. Reyes-Rodríguez (1728958)
A1 Karl Anker Jørgensen (1287900)
A1 Chenxi Lu (2737222)
A1 K. N. Houk (1247004)
YR 2021
K1 Biophysics
K1 Biochemistry
K1 Medicine
K1 Genetics
K1 Molecular Biology
K1 Evolutionary Biology
K1 Immunology
K1 Developmental Biology
K1 Infectious Diseases
K1 Computational Biology
K1 Biological Sciences not elsewhere classified
K1 Information Systems not elsewhere classified
K1 stereoselective S N 2 reaction
K1 model example
K1 chiral aminocatalyst
K1 quaternary carbon stereocenter
K1 studies elucidates
K1 Asymmetric S N 2 Dynamic Kinetic Re
K1 equilibrating mixture
K1 stereogenic center
K1 future reactions
K1 Walden cycle
K1 racemic mixture
K1 enantioenriched products
K1 S N 2- type displacement
K1 substitution proceeding
K1 Walden inversion
K1 stereospecific backside attack
K1 predefined stereocenters
K1 S N 2 mechanism
K1 enantioconvergent reaction proceeds
K1 S N 2 reaction exhibits
K1 S N 2 reaction
K1 chiral organocatalyst
K1 examples challenge
K1 S N 2
K1 principle
JF https://figshare.com/articles/journal_contribution/An_Asymmetric_S_sub_N_sub_2_Dynamic_Kinetic_Resolution/14535656
LK http://dx.doi.org/https://doi.org/10.1021/jacs.1c02193.s001
DO https://doi.org/10.1021/jacs.1c02193.s001
SF ELIB - SuUB Bremen

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