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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
A Unifying Bioinspired Synthesis of (−)-Asperaculin A and (−)-Penifulvin D
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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