Publications

  1. Veth, L.;# Grab, H.;# Martinez, S.;# Antheaume, C.; Dydio, P. ChemRxiv 2021 Transfer C-H Borylation of Alkenes under Rh(I)-Catalysis: In-sight into the Mechanism, Selectivity-Control & Synthetic Capacity

    # -equal contribution

10.33774/chemrxiv-2021-0qqwv

  1. Lainer, B.; Lichosyt, D.; Aleksandrova, M.; Dydio, P. J. Org. Chem. 2021, ASAP Article: Enantioselective α-Arylation of Primary Alcohols under Sequential One-Pot Catalysis.

https://pubs.acs.org/doi/10.1021/acs.joc.1c00983

  1. Casnati, A.;# Lichosyt, D.;# Lainer, B.; Veth, L.; Dydio, P. Org. Lett. 2021, 23, 3502-3506: Multi-catalytic Approach to One-pot Stereoselective Synthesis of Secondary Benzylic Alcohols.

    # -equal contribution

https://pubs.acs.org/doi/10.1021/acs.orglett.1c00939

pre-print open-access (chemrxive)

  1. Martinez, S.;# Veth, L.;# Lainer, B.; Dydio, P.  ACS Catal.  2021, 11, 3891-3915:  Challenges and Opportunities in Multicatalysis.

    # -equal contribution

https://pubs.acs.org/doi/10.1021/acscatal.0c05725

  1. Zhang, Y.; Torker, S.; Sigrist, M.; Bregovic, N.; Dydio, P.  J. Am. Chem. Soc.  2020, 142, 18251-18265:  Binuclear Pd(I)-Pd(I) Catalysis Assisted by Iodide Ligands for Selective Hydroformylation of Alkenes and Alkynes.

https://dx.doi.org/10.1021/jacs.0c09254

post-print open-access (OAK)

  1. Lichosyt, D.; Zhang, Y.; Hurej, K.; Dydio, P. Nature Catal.  2019, 2, 114: Dual-Catalytic Transition Metal Systems for Functionalization of Unreactive Sites of Molecules.

https://doi.org/10.1038/s41929-018-0207-1

  1. Lichosyt, D.; Wasiłek, S.; Dydio, P.; Jurczak, J. Chem. Eur. J. 2018, 24, 11683: The influence of binding site geometry on anion binding selectivity: a case study of macrocyclic receptors built on an azulene skeleton.

https://onlinelibrary.wiley.com/doi/abs/10.1002/chem.201801460

Previous research (prior at University of Strasbourg): 

  1. Key, H. M.;#, Dydio, P.;# Liu, Z.; Rha, J. Y-E.; Nazarenko, A.; Seyedkazemi, V.; Clark, D. S.; Hartwig, J. H. ACS Cent. Sci. 2017, 3, 302: Beyond Iron: Iridium-Containing P450 Enzymes for Highly Selective Cyclopropanations of Structurally Diverse Alkenes.

# -equal contribution

https://pubs.acs.org/doi/full/10.1021/acscentsci.6b00391

  1.  Dydio, P.;# Key, H. M.;#, Hayashi, H.; Clark, D. S.; Hartwig, J. H.  J. Am. Chem. Soc. 2017, 139, 1750: Enzymatic, Chemoselective C-H Amination Catalyzed by CYP119 Containing an Ir(Me)-PIX Cofactor.

# -equal contribution

https://pubs.acs.org/doi/abs/10.1021/jacs.6b11410

– Highlighted in JACS 2017, 139, 1705

  1. Dydio, P.;# Key, H. M.;# Nazarenko, A.; Rha, J. Y-E.; Seyedkazemi, V.; Clark, D. S.; Hartwig, J. H. Science, 2016, 354, 102-106: An artificial metalloenzyme with the kinetics of native enzymes.

# -equal contribution  

http://science.sciencemag.org/content/354/6308/102

– Highlighted in Chemical & Engineering News 2016, 94, 8

  1. Key, H. M.;# Dydio, P.;# Clark, D. S.; Hartwig, J. H. Nature, 2016, 534, 534-537: Artificial Catalysis by Heme Proteins Containing Noble Metal Porphyrins.

# -equal contribution

http://www.nature.com/nature/journal/vaop/ncurrent/abs/nature17968.html

– Highlighted in Chemical & Engineering News 2016, 25, 6

– Highlighted in Nature 2016, 537, 156

– Highlighted in Angew. Chem. In. Ed. 2016 (10.1002/anie.201607222)

– Highlighted in Chemistry World RSC, 6/14/2016: Metal ion swap improves artificial enzymes

– Highlighted in Nature Podcast on 06/16/2016

– Highlighted in The Daily Californian, 7/04/2016: Berkeley Lab researchers combine synthetic, natural catalysts to create new reactions

  1. Bai, S.-T.; Sinha, V.; Kluwer, A. M.; Linnebank, P. R.; Abiri, Z.; Dydio, P.; Lutz, M.; de Bruin, B.; Reek, J. N. H. Chem. Sci. 2019, 10 (31), 7389–7398: Effector Responsive Hydroformylation Catalysis.

https://pubs.rsc.org/en/content/articlelanding/2019/sc/c9sc02558h#!divAbstract

  1. Théveau, L.; Bellini, R.; Dydio, P.; Szabo, Z.; van der Werf, A.; Sander, R. A.; Reek, J. N. H.; Moberg, C. Organometallics, 2016, 1956–1963: Cofactor-Controlled Chirality of Tropoisomeric Ligand.

http://pubs.acs.org/doi/abs/10.1021/acs.organomet.6b00265

  1. Dydio, P.; Reek, J. N. H. Chem. Sci. 2014, 5, 2135−2145: Supramolecular control of selectivity in transition metal catalysis through substrate preorganization. REVIEW

http://pubs.rsc.org/en/Content/ArticleLanding/2014/SC/c3sc53505c#!divAbstract

  1. Dydio, P.; Detz, R. J.; de Bruin, B.; Reek, J. N. H. J. Am. Chem. Soc. 2014, 136, 8418–8429: Beyond Classical Reactivity Patterns: Hydroformylation of Vinyl and Allyl Arenes to Valuable b-and g-Aldehyde Intermediates using Supramolecular Catalysis.

http://pubs.acs.org/doi/abs/10.1021/ja503033

  1. Dydio, P.; Reek, J. N. H. Nat. Protoc. 2014, 9, 1183−1191: Scalable and chromatography-free synthesis of 2-(2-formylalkyl)arenecarboxylic acid derivatives through the supramolecularly controlled hydroformylation of vinylarene-2-carboxylic acids.

http://www.nature.com/nprot/journal/v9/n5/full/nprot.2014.077.html

  1. Dydio, P.; Breuil, P.-A. R.; Reek, J. N. H. Isr. J. Chem. 2013, 53, 61-74: Dynamic Combinatorial Chemistry in Chemical Catalysis. REVIEW

http://onlinelibrary.wiley.com/doi/10.1002/ijch.201200083/abstract                          

  1. Dydio, P.; Ploeger, M.; Reek, J. N. H. ACS Catal. 2013, 3, 2939–2942: Selective Isomerization-Hydroformylation Sequence: a Strategy to Valuable α-Methyl-Branched Aldehydes from Terminal Olefins.

http://pubs.acs.org/doi/abs/10.1021/cs400872a

  1. Dydio, P.; Detz, R. J.; Reek, J. N. H. J. Am. Chem. Soc. 2013, 135, 10817-10828: Precise Supramolecular Control of Selectivity in the Rh-catalyzed Hydroformylation of Terminal and Internal Alkenes.

http://pubs.acs.org/doi/abs/10.1021/ja4046235

  1. Dydio, P.; Reek, J. N. H. Angew. Chem., Int. Ed. 2013, 52, 3878-3882: Supramolecular control of selectivity in hydroformylation of vinyl arenes: easy access to valuable b-aldehyde intermediates.

http://onlinelibrary.wiley.com/doi/10.1002/anie.201209582/abstract

– Very Important Paper and Back Cover Art Article

– Highlighted in Nat. Chem. 2013, 5, 250                                                                                                                 

  1. Dydio, P.; Rubay, C.; Gadzikwa, T.; Lutz, M.; Reek, J. N. H. J. Am. Chem. Soc. 2011, 133, 17176-17179: “Cofactor”-Controlled Enantioselective Catalysis.

http://pubs.acs.org/doi/abs/10.1021/ja208589c

– Highlighted in Chemical & Engineering News 2011, 89, 13

– Highlighted in Chemistry World RSC, 10/18/2011: Cofactor control of catalysis enantioselectivity

  1. Dydio, P.; Dzik, W. I.; Lutz, M.; de Bruin, B.; Reek, J. N. H. Angew. Chem., Int. Ed. 2011, 50, 396-400: Remote Supramolecular Control of Catalyst Selectivity in the Hydroformylation of Alkenes.

http://onlinelibrary.wiley.com/doi/10.1002/anie.201005173/abstract

– HOT paper and Back Cover Art Article

– Highlighted in ChemCatChem 2011, 3, 619-621

– Highlighted in Wiley ChemistryViews, 01/24/2011: Control of Selectivity in Hydroformylation

  1. Lichosyt, D.; Dydio, P.; Jurczak, J. Chem. Eur. J. 2016, 22, 17673: Phosphate Anion Sensing by Azulene-Based Macrocyclic Receptors.

https://onlinelibrary-wiley-com/doi/abs/10.1002/chem.201603555

  1. Jurczak, J.; Dydio, P.; Stepniak, P.; Zieliński, T. Sensor Actuat B Chem. 2016, 237, 621–627: Diamidonaphthalenodipyrrole-derived Fluorescent Sensors for Anions.

http://www.sciencedirect.com/science/article/pii/S0925400516310048

  1. Jurczak, J.; Dydio, P.; Stepniak, P.; Zieliński, T. RSC Adv. 2016, 6, 41568-41571: A hybrid macrocyclic anion receptor exploiting the pyrrole-2,5-diacetamide unit.


http://pubs.rsc.org/en/content/articlelanding/2016/ra/c6ra05804c#!divAbstract

  1. Dydio, P.; Lichosyt, D.; Jurczak, J. Chem. Soc. Rev. 2011, 40, 2971-2985: Amide- and urea-functionalized pyrroles and benzopyrroles as synthetic, neutral anion receptors.

http://pubs.rsc.org/en/content/articlelanding/2011/cs/c1cs15006e#!divAbstract

  1. Dydio, P.; Lichosyt, D.; Zieliński, T.; Jurczak, J. Chem. Eur. J. 2012, 18, 13686-13701: 7,7’-Diamino-2,2’-diindolylmethane: a Building Block for Highly Efficient and Selective Anion Receptors Studies in Solution and in the Solid State.

http://onlinelibrary.wiley.com/doi/10.1002/chem.201201909/abstract

  1. Jurczak, J.; Chmielewski, M. J.; Dydio, P.; Lichosyt, D.; Ulatowski, F.; Zieliński, T. Pure Appl. Chem. 2011, 83, 1543-1554: Benzopyrrole derivatives as effective anion receptors in highly competitive solvents.

https://www.degruyter.com/view/j/pac.2011.83.issue-8/pac-con-10-11-11/pac-con-10-11-11.xml

  1. Dydio, P.; Zieliński, T.; Jurczak, J. Org. Lett. 2010, 12, 1076-1078: 7,7′-Diureido-2,2′-diindolylmethanes: Anion Receptors Effective in a Highly Competitive Solvent, Methanol.

http://pubs.acs.org/doi/abs/10.1021/ol1000395

  1. Dydio, P.; Zieliński, T.; Jurczak, J. Chem. Commun. 2009, 4560-4562:
    Anion receptors based on 7,7’-diamido-2,2’-diindolylmethane.

http://pubs.rsc.org/en/Content/ArticleLanding/2009/CC/b907164d#!divAbstract

  1. Dydio P.; Zieliński T.; Jurczak, J. J. Org. Chem. 2009, 74, 1525-1530:
    Bishydrazide Derivatives of Isoindoline as Simple Anion Receptors.

http://pubs.acs.org/doi/abs/10.1021/jo802288u?journalCode=joceah

  1. Zieliński T.; Dydio P.; Jurczak, J. Tetrahedron 2008, 64, 568-574: Synthesis, structure and the binding properties of the amide-based anion receptors derived from 1H-indole-7-amine.

http://www.sciencedirect.com/science/article/pii/S0040402007018947