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Synthesis of the Lipophilic Amine Tail of Abediterol Enable..:

Jorge García-Lacuna (5645996) ; Tobias Fleiß (10296850) ; Rachel Munday (7513727)...
https://figshare.com/articles/journal_contribution/Synthesis_of_the_Lipophilic_Amine_Tail_of_Abediterol_Enabled_by_Multiphase_Flow_Transformations/14179549. , 2021

Link: https://doi.org/10.1021/acs.oprd.1c00002.s001

RT Journal
T1 <Title>Synthesis of the Lipophilic Amine Tail of Abediterol Enabled by Multiphase Flow Transformations</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonian:oai:figshare.com:article_14179549&Exemplar=1&LAN=DE
				
A1 Jorge García-Lacuna (5645996)
A1 Tobias Fleiß (10296850)
A1 Rachel Munday (7513727)
A1 Kevin Leslie (1324953)
A1 Anne O'Kearney-McMullan (1546210)
A1 Christopher A. Hone (4090777)
A1 C. Oliver Kappe (1264179)
YR 2021
K1 Biochemistry
K1 Molecular Biology
K1 Pharmacology
K1 Biotechnology
K1 Environmental Sciences not elsewhere classified
K1 Chemical Sciences not elsewhere classified
K1 mol
K1 Multiphase Flow Transformations
K1 continuous-flow
K1 sequence
K1 lipophilic amine tail portion
K1 Ru-catalyzed reductive amination
K1 Lipophilic Amine Tail
K1 reductive amination
K1 hydroformylation
K1 ruthenium-catalyzed reductive amination
K1 amine tail
K1 23 min residence time
K1 flow
K1 Abediterol
K1 O-alkylation
K1 optimized
K1 drug candidate precursor
JF https://figshare.com/articles/journal_contribution/Synthesis_of_the_Lipophilic_Amine_Tail_of_Abediterol_Enabled_by_Multiphase_Flow_Transformations/14179549
LK http://dx.doi.org/https://doi.org/10.1021/acs.oprd.1c00002.s001
DO https://doi.org/10.1021/acs.oprd.1c00002.s001
SF ELIB - SuUB Bremen

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