Zobrazeno 1 - 10
of 134
pro vyhledávání: '"Anne Fiksdahl"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 17, Iss 1, Pp 186-192 (2021)
Chiral cyclam (1,4,8,11-tetraazacyclotetradecane) derivatives were synthesized stepwise from chiral mono-Boc-1,2-diamines and (dialkyl)malonyl dichloride via open diamide-bis(N-Boc-amino) intermediates (65–91%). Deprotection and ring closure with a
Externí odkaz:
https://doaj.org/article/dba2f29b08254ed7b746c9874858b663
Publikováno v:
Results in Chemistry, Vol 4, Iss , Pp 100360- (2022)
Au(III)-NHC-oxazolyl complexes are prepared by oxidation and anion exchange of the corresponding Au(I)Cl-NHC-oxazolyl precursors, which are synthesized from appropriate imidazolium pre-ligands. As the Au(III) complexes are too unstable for proper iso
Externí odkaz:
https://doaj.org/article/19cad5110fb84152a1b1236ba84f9dc1
Autor:
Kallidanthiyil Chellappan Lethesh, Sigvart Evjen, Jaganathan Joshua Raj, Denis C. D. Roux, Vishwesh Venkatraman, Kaushik Jayasayee, Anne Fiksdahl
Publikováno v:
Frontiers in Chemistry, Vol 7 (2019)
Structurally modified hydroxyl functionalized pyridinium ionic liquids (ILs), liquid at room temperature, were synthesized and characterized. Alkylated N-(2-hydroxyethyl)-pyridinium ILs were prepared from alkylpyridines via corresponding bromide salt
Externí odkaz:
https://doaj.org/article/2a475bd467b14b2fb699abe0dc357c38
Autor:
Anne Fiksdahl, Freddy Tjosaas
Publikováno v:
Molecules, Vol 11, Iss 2, Pp 130-133 (2006)
The nitro group of methyl 3-nitropyridine-4-carboxylate (1) has successfully been replaced by fluoride anion via nucleophilic aromatic substitution to give the 3-fluoro- pyridine-4-carboxylate 2.
Externí odkaz:
https://doaj.org/article/c7f54163603347bc9947a0a6f42a567e
Publikováno v:
Molecules, Vol 11, Iss 1, Pp 103-114 (2006)
The content and distribution of stilbenes and resin acids in Scots pine (Pinus sylvestris) and spruce (Picea abies), sampled in central Norway, have been examined. The contents of pinosylvin stilbenes in pine heartwood/living knots were 0.2-2/2-8 % (
Externí odkaz:
https://doaj.org/article/10f4923dabc445b6ba3f073427b30473
Autor:
Anne Fiksdahl, Curt Wentrup
Publikováno v:
ARKIVOC, Vol 2000, Iss 3, Pp 438-444 (2000)
Externí odkaz:
https://doaj.org/article/b8f69d209de04f51b8117968a86202d6
Publikováno v:
Arkivoc. 2023
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::08d79e066fe3300bb14ff88939c93030
https://doi.org/10.24820/ark.5550190.p011.969
https://doi.org/10.24820/ark.5550190.p011.969
Publikováno v:
Dalton Transactions. 50:5128-5138
Five pairs of novel chiral alcohol functionalised gold(i) and gold(iii) NHC complexes derived from chiral amino alcohols, were synthesized and characterised (NMR, IR, HRMS). Single crystal X-ray diffraction data of gold(i) and gold(iii) complexes are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::878135fe9444f997b27189e627bab95b
https://doi.org/10.1039/d1dt00387a
https://doi.org/10.1039/d1dt00387a
Autor:
Stefano Battaglia, Roland Lindh, Ann Christin Reiersølmoen, Máté Erdélyi, Andreas Orthaber, Anne Fiksdahl
Publikováno v:
Inorganic Chemistry
Gold(III) complexes are versatile catalysts offering a growing number of new synthetic transformations. Our current understanding of the mechanism of homogeneous gold(III) catalysis is, however, limited, with that of phosphorus-containing complexes b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::324f29ae8459f4a1ac6504bc720795a9
http://europepmc.org/articles/PMC7927145
http://europepmc.org/articles/PMC7927145
Publikováno v:
Synthetic Communications. 50:1758-1773
Novel chiral menthol-based pyridyl nitrone ligands were synthesized and Au(I) coordination of the ligands gave chiral Au(I)���nitrone complexes. 1H NMR studies of the gold(I) coordination experiments with nitrone ligands afforded a convenient m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82555a2f7a96da75d1c78bbab29312ee
https://doi.org/10.1080/00397911.2020.1731550
https://doi.org/10.1080/00397911.2020.1731550