| 1. |
- Abdel-Magied, Ahmed, et al.
(author)
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Diastereomeric control of enantioselectivity: evidence for metal cluster catalysis.
- 2014
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In: Chemical Communications. - : Royal Society of Chemistry (RSC). - 1364-548X. ; 50:57, s. 7705-7708
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Journal article (peer-reviewed)abstract
- Enantioselective hydrogenation of tiglic acid effected by diastereomers of the general formula [(μ-H)2Ru3(μ3-S)(CO)7(μ-P-P*)] (P-P* = chiral Walphos diphosphine ligand) strongly supports catalysis by intact Ru3 clusters. A catalytic mechanism involving Ru3 clusters has been established by DFT calculations.
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| 2. |
- Ahlsten, Nanna, 1982-, et al.
(author)
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Ir-catalysed formation of C-F bonds. From allylic alcohols to α-fluoroketones
- 2011
-
In: Chemical Communications. - : Royal Society of Chemistry (RSC). - 1359-7345 .- 1364-548X. ; 47:29, s. 8331-8333
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Journal article (peer-reviewed)abstract
- A novel iridium-catalysed tandem isomerisation/C-F bond formation from allylic alcohols and Selectfluor® to prepare α-fluorinated ketones as single constitutional isomers is reported.
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| 3. |
- Andersson, Hans, et al.
(author)
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Efficient, mild and completely regioselective synthesis of substituted pyridines
- 2010
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In: Chemical Communications. - : RSC Publishing. - 1359-7345 .- 1364-548X. ; 46:19, s. 3384-3386
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Journal article (peer-reviewed)abstract
- Addition of Grignard reagents to pyridine N-oxides in THF at low temperature (-78 to -20 °C) and treatment with TFAA provides an efficient general procedure for synthesis of substituted pyridines. The method is compatible with a range of functional groups such as esters, halogens and nitriles.
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| 4. |
- Ankner, Tobias, 1976, et al.
(author)
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Selective cleavage of 3,5-bis-(trifluoromethyl)benzylcarbamate by SmI2-Et3N-H2O
- 2013
-
In: Chemical Communications. - : Royal Society of Chemistry (RSC). - 1359-7345 .- 1364-548X. ; 49:61, s. 6867-6869
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Journal article (peer-reviewed)abstract
- A novel electron poor protection group for amines has been developed. It undergoes rapid cleavage by SmI2-Et3N-H2O and its orthogonality towards the regular benzyl carbamate group (CBz) under reductive or transfer hydrogenolytic conditions is reported.
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| 5. |
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| 6. |
- Berghaus, Melanie, et al.
(author)
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Productive encounter : molecularly imprinted nanoparticles prepared using magnetic templates
- 2014
-
In: Chemical Communications. - : Royal Society of Chemistry. - 1359-7345 .- 1364-548X. ; 50:64, s. 8993-8996
-
Journal article (peer-reviewed)abstract
- Synthesis of core-shell nanoparticles by surface initiated reversible addition fragmentation chain transfer polymerization in presence of a chiral template conjugated to magnetic nanoparticles is reported. The approach leads to imprinted nanoparticles featuring enantioselectivity and enhanced affinity compared to nanoparticles prepared using free template.
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| 7. |
- Beyler, Maryline, et al.
(author)
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Pentacoordinate iron complexes as functional models of the distal iron in [FeFe] hydrogenases
- 2011
-
In: Chemical Communications. - : Royal Society of Chemistry (RSC). - 1359-7345 .- 1364-548X. ; 47:42, s. 11662-11664
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Journal article (peer-reviewed)abstract
- Mononuclear pentacoordinate iron complexes with a free coordination site were prepared as mimics of the distal Fe (Fe(d)) in the active site of [FeFe] hydrogenases. The complexes catalyze the electrochemical reduction of protons at mild overpotential.
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| 8. |
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| 9. |
- Borg, Tessie, et al.
(author)
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Mukaiyama aldol addition to α-chloro-substituted aldehydes. Origin of the unexpected syn selectivity.
- 2010
-
In: Chemical Communications. - : Royal Society of Chemistry (RSC). - 1359-7345 .- 1364-548X. ; 46:8, s. 1281-1283
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Journal article (peer-reviewed)abstract
- The addition of sterically demanding enolsilanes to alpha-chloro aldehydes results unexpectedly in preferential formation of the anti-PFA product (1,2-syn), while the addition of the corresponding boron enolate furnishes the expected polar Felkin-Anh product (1,2-anti). A stereoinduction model explaining these observations is proposed.
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| 10. |
- Borgström, Björn, et al.
(author)
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Synthetic modification of salinomycin: selective O-acylation and biological evaluation
- 2013
-
In: Chemical Communications. - : Royal Society of Chemistry (RSC). - 1364-548X .- 1359-7345. ; 49:85, s. 9944-9946
-
Journal article (peer-reviewed)abstract
- Salinomycin has found renewed interest as an agent for prevention of cancer recurrence through selectively targeting cancer stem cells. Strategies for generation of improved salinomycin analogs by individual modification of its hydroxyl groups are presented. An evaluation of the dose-response effects of the resulting library on breast cancer cell lines shows that acylation of the C20 hydroxyl can be used to improve IC50 values down to one fifth that of salinomycin.
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