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A Unifying Bioinspired Synthesis of (−)-Asperaculin A and (..:

Ian R. George (10573226) ; Miguel López-Tena (10573229) ; Anders P. Sundin (8115563).
https://figshare.com/articles/journal_contribution/A_Unifying_Bioinspired_Synthesis_of_-Asperaculin_A_and_-Penifulvin_D/14388530. , 2021

Link: https://doi.org/10.1021/acs.orglett.1c00955.s001

RT Journal
T1 <Title>A Unifying Bioinspired Synthesis of (−)-Asperaculin A and (−)-Penifulvin D</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonian:oai:figshare.com:article_14388530&Exemplar=1&LAN=DE
				
A1 Ian R. George (10573226)
A1 Miguel López-Tena (10573229)
A1 Anders P. Sundin (8115563)
A1 Daniel Strand (1327521)
YR 2021
K1 Biophysics
K1 Biochemistry
K1 Medicine
K1 Ecology
K1 Marine Biology
K1 Computational Biology
K1 Biological Sciences not elsewhere classified
K1 Chemical Sciences not elsewhere classified
K1 reversal
K1 Density
K1 ether substituent
K1 theory calculations
K1 BV
K1 selectivity
K1 Penifulvin
K1 peracid
K1 cyanation
K1 cyanohydrin
K1 photocycloaddition
K1 polycyclic carbon framework
K1 Synthetic features
K1 Asperaculin
K1 Baeyer
K1 choice
K1 diastereoselective meta
K1 synthese
K1 oxidant
K1 isomeric dioxafenestrene
K1 bioinspired
K1 ketone
K1 nonaqueous hydrolysis
K1 aryl α- position
K1 interaction
K1 lactone motif accounts
K1 Unifying Bioinspired Synthesis
JF https://figshare.com/articles/journal_contribution/A_Unifying_Bioinspired_Synthesis_of_-Asperaculin_A_and_-Penifulvin_D/14388530
LK http://dx.doi.org/https://doi.org/10.1021/acs.orglett.1c00955.s001
DO https://doi.org/10.1021/acs.orglett.1c00955.s001
SF ELIB - SuUB Bremen

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