
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
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.
– J Am Chem Soc
(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
– Journal of the American Chemical Society
(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)
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