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One-Carbon Insertion and Polarity Inversion Enabled a Pyrro..:

Donghui Ma (1399846) ; Brandon S. Martin (6056747) ; Katelyn S. Gallagher (11486580)..
https://figshare.com/articles/journal_contribution/One-Carbon_Insertion_and_Polarity_Inversion_Enabled_a_Pyrrole_Strategy_to_the_Total_Syntheses_of_Pyridine-Containing_i_Lycopodium_i_Alkaloids_Complanadine_A_and_Lycodine/16689234. , 2021

Link: https://doi.org/10.1021/jacs.1c08626.s001

RT Journal
T1 <Title>One-Carbon Insertion and Polarity Inversion Enabled a Pyrrole Strategy to the Total Syntheses of Pyridine-Containing Lycopodium Alkaloids: Complanadine A and Lycodine</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonian:oai:figshare.com:article_16689234&Exemplar=1&LAN=DE
				
A1 Donghui Ma (1399846)
A1 Brandon S. Martin (6056747)
A1 Katelyn S. Gallagher (11486580)
A1 Takeru Saito (11486583)
A1 Mingji Dai (1265700)
YR 2021
K1 Biophysics
K1 Biochemistry
K1 Genetics
K1 Molecular Biology
K1 Pharmacology
K1 Biotechnology
K1 Ecology
K1 Inorganic Chemistry
K1 Science Policy
K1 Space Science
K1 Environmental Sciences not elsewhere classified
K1 Biological Sciences not elsewhere classified
K1 tetracyclic skeleton via
K1 pot staudinger reduction
K1 persistent pain management
K1 also simultaneously introduced
K1 >- markovnikov hydroazidation
K1 key steps include
K1 pyridine precursor allowed
K1 polarity inversion enabled
K1 containing tetracyclic skeleton
K1 concise total syntheses
K1 carbon insertion process
K1 pyrrole strategy enabled
K1 total syntheses
K1 polarity inversion
K1 carbon insertion
K1 pyrrole strategy
K1 11 steps
K1 type cyclization
K1 representative members
K1 rapid construction
K1 pyrrole group
K1 lycopodium </
K1 ketone condensation
K1 desired pyridine
K1 characteristic pyridine
K1 anti </
JF https://figshare.com/articles/journal_contribution/One-Carbon_Insertion_and_Polarity_Inversion_Enabled_a_Pyrrole_Strategy_to_the_Total_Syntheses_of_Pyridine-Containing_i_Lycopodium_i_Alkaloids_Complanadine_A_and_Lycodine/16689234
LK http://dx.doi.org/https://doi.org/10.1021/jacs.1c08626.s001
DO https://doi.org/10.1021/jacs.1c08626.s001
SF ELIB - SuUB Bremen

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