University Assistant Professor
Research
The Dydio group is researching new ways to improve the efficiency and capacity of organic synthesis.
Areas of interest include:
- Complex Networks of Reactions
- Mechanism-based design of new transformations
- Advancing key industrial processes driven by elucidating their mechanistic features
Watch Dr Dydio discuss his research
Publications
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 ReceptorsuStudies in Solution and in the Solid State
Chemistry – A European Journal
(2012)
18
13686
(doi: 10.1002/chem.201201909)
"Cofactor"-controlled enantioselective catalysis.
J Am Chem Soc
(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.
Organic letters
(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)
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