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- Currently displaying 21 - 40 of 42 publications
An artificial metalloenzyme with the kinetics of native enzymes.
Science (New York, N.Y.)
(2016)
354
102
(doi: 10.1126/science.aah4427)
Abiological catalysis by artificial haem proteins containing noble metals in place of iron.
Nature
(2016)
534
534
(doi: 10.1038/nature17968)
Cofactor-Controlled Chirality of Tropoisomeric Ligand
Organometallics
(2016)
35
1956
A hybrid macrocyclic anion receptor exploiting the pyrrole-2,5-diacetamide unit
RSC Advances
(2016)
6
41568
(doi: 10.1039/c6ra05804c)
Beyond Classical Reactivity Patterns: Hydroformylation of Vinyl and Allyl Arenes to Valuable β- and γ-Aldehyde Intermediates Using Supramolecular Catalysis
Journal of the American Chemical Society
(2014)
136
8418
(doi: 10.1021/ja503033q)
Scalable and chromatography-free synthesis of 2-(2-formylalkyl)arenecarboxylic acid derivatives through the supramolecularly controlled hydroformylation of vinylarene-2-carboxylic acids.
Nature protocols
(2014)
9
1183
(doi: 10.1038/nprot.2014.077)
Supramolecular control of selectivity in transition-metal catalysis through substrate preorganization
Chem. Sci.
(2014)
5
2135
(doi: 10.1039/c3sc53505c)
Selective Isomerization–Hydroformylation Sequence: A Strategy to Valuable α‑Methyl-Branched Aldehydes from Terminal Olefins
ACS Catalysis
(2013)
3
2939
(doi: 10.1021/cs400872a)
Precise supramolecular control of selectivity in the Rh-catalyzed hydroformylation of terminal and internal alkenes.
J Am Chem Soc
(2013)
135
10817
(doi: 10.1021/ja4046235)
Supramolecular Control of Selectivity in Hydroformylation of Vinyl Arenes: Easy Access to Valuable β‐Aldehyde Intermediates
Angewandte Chemie
(2013)
125
3970
(doi: 10.1002/ange.201209582)
Supramolecular control of selectivity in hydroformylation of vinyl arenes: easy access to valuable β-aldehyde intermediates.
Angew Chem Int Ed Engl
(2013)
52
3878
(doi: 10.1002/anie.201209582)
Dynamic Combinatorial Chemistry in Chemical Catalysis
Israel Journal of Chemistry
(2013)
53
61
(doi: 10.1002/ijch.201200083)
7,7'-Diamino-2,2'-diindolylmethane: a building block for highly efficient and selective anion receptors-studies in solution and in the solid state.
Chemistry – A European Journal
(2012)
18
13686
(doi: 10.1002/chem.201201909)
“Cofactor”-Controlled Enantioselective Catalysis
Journal of the American Chemical Society
(2011)
133
17176
(doi: 10.1021/ja208589c)
Benzopyrrole derivatives as effective anion receptors in highly competitive solvents
Pure and Applied Chemistry
(2011)
83
1543
(doi: 10.1351/pac-con-10-11-11)
Amide - and urea-functionalized pyrroles and benzopyrroles as synthetic, neutral anion receptors
Chem Soc Rev
(2011)
40
2971
(doi: 10.1039/c1cs15006e)
Remote Supramolecular Control of Catalyst Selectivity in the Hydroformylation of Alkenes
Angewandte Chemie
(2011)
123
416
(doi: 10.1002/ange.201005173)
Remote Supramolecular Control of Catalyst Selectivity in the Hydroformylation of Alkenes
Angewandte Chemie International Edition
(2011)
50
396
(doi: 10.1002/anie.201005173)
7,7'-Diureido-2,2'-diindolylmethanes: anion receptors effective in a highly competitive solvent, methanol.
Org Lett
(2010)
12
1076
(doi: 10.1021/ol1000395)
Anion receptors based on 7,7'-diamido-2,2'-diindolylmethane.
Chemical Communications
(2009)
4560
(doi: 10.1039/b907164d)