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2020 - 2024
Independent Publications

Synthesis of 4-Phenylpyrrolidin-2-one via an Aza-BaeyerVilliger Rearrangement
Org. Synth. 2023, 100, 347-360
Mike Ong#, Marlene Arnold#, Johannes M. Wahl

https://doi.org/10.15227/orgsyn.100.0347

From Cycloalkanols to Heterocycles via Nitrogen Insertion
Org. Lett. 2023, 25, 5795–5799
Alexander Sandvoß, Johannes M. Wahl
Highlighted in OPR&D
Highlighted in Synfacts

OPR&D:
https://doi.org/10.1021/acs.oprd.3c00291

https://doi.org/10.1021/acs.orglett.3c02048

Synfacts:
https://doi.org/10.1055/s-0042-1752039

Wacker Oxidation of Methylenecyclobutanes: Scope and Selectivity in an Unusual Setting
Angew. Chem. Int. Ed. 2023, e202215381.
Jan Sietmann#, Marius Tenberge#, Johannes M. Wahl
*Highlighted in Synfacts

https://doi.org/10.1002/anie.202215381

Synfacts:
https://doi.org/10.1055/s-0042-1753356

Lewis Acid Catalysed Asymmetric One-Carbon Ring-Expansion of Prochiral Cyclobutanones
Synthesis 2023, 55, 892.
Marius Tenberge, Johannes M. Wahl

https://doi.org/10.1055/s-0042-1751386

Synthesis 2022_Marius.png

Stereospecific Nitrogen Insertion Using Amino Diphenyl-phosphinates: An Aza-Baeyer-Villiger Rearrangement
Org. Lett. 2022, 24, 6171.
Mike Ong, Marlene Arnold, Alexander W. Walz, Johannes M. Wahl
*Highlighted in Synfacts

https://doi.org/10.1021/acs.orglett.2c02361

Synfacts:
https://www.doi.org/10.1055/s-0042-1751812

Dynamic kinetic resolution of transient hemiketals: a strategy for the desymmetrisation of prochiral oxetanols
Chem. Sci. 2022, 13, 6297.
Alexander Sandvoß, Henning Maag, Constantin G. Daniliuc,
Dieter Schollmeyer, Johannes M. Wahl

https://doi.org/10.1039/D2SC01547A

Desymmetrization of Prochiral Cyclobutanones via Nitrogen Insertion: A Concise Route to Chiral γ‐Lactams
Angew. Chem. Int. Ed. 2021, 60, 9719.
Jan Sietmann,# Mike Ong,# Christian Mück-Lichtenfeld, Constantin G. Daniliuc, Johannes M. Wahl

https://doi.org/10.1002/anie.202100642

Recent Advances in Enantioselective Desymmetrizations of Prochiral Oxetanes
Chem. Eur. J. 2021, 27, 5871.
Alexander Sandvoß and Johannes M. Wahl

https://doi.org/10.1002/chem.202004923

Enantioselective Desymmetrization of Cyclobutanones:
A Speedway to Molecular Complexity
Angew. Chem. Int. Ed. 2020, 59, 6964.
Jan Sietmann and Johannes M. Wahl

https://doi.org/10.1002/anie.201910767

2012 - 2019

Supervised Publications

Thioallenoates in Catalyic Enantioselective [2+2]-Cycloadditions with Unactivated Alkenes
Tetrahedron, 2019, 75, 3265.
Michael L. Conner, Johannes M. Wahl, M. Kevin Brown

https://doi.org/10.1016/j.tet.2019.04.028

Recent Advances in the Synthesis of Gem-Dimethylcyclobutane Natural Products
Nat. Prod. Rep. 2019, 36, 1383.
Erin N. Hancock, Johannes M. Wahl, M. Kevin Brown

https://doi.org/10.1039/c8np00083b

Allenoates in Enantioselective [2+2] Cycloadditions: From a Mechanistic Curiosity to a Stereospecific Transformation
J. Am. Chem. Soc. 2018, 140, 15943.
Johannes. M. Wahl, Michael L. Conner, M. Kevin Brown

https://doi.org/10.1021/jacs.8b10008

Synthesis of (−)-Hebelophyllene E: An Entry to Geminal Dimethylcyclobutanes by [2+2] Cycloaddition of Alkenes and Allenoates
Angew. Chem. Int. Ed. 2018, 57, 4647.
Johannes M. Wahl, Michael L. Conner, M. Kevin Brown
*Highlighted in Synfacts

https://doi.org/10.1002/anie.201801110

Synfacts:
https://doi.org/10.1055/s-0037-1609842

https://doi.org/10.1021/acs.joc.6b01298

A Route to 2-Substituted 3-Cyanopyrroles: Synthesis of Danaidal and Suffrutine A
J. Org. Chem. 2016, 81, 6149.
Johannes M. Wahl and Thorsten Bach

Pyrrole as a Directing Group: Regioselective Pd(II)-Catalyzed Alkylation and Benzylation at the Benzene Core of 2-Phenylpyrroles
Org. Lett. 2016, 18, 852.
Johannes M. Wahl, Alexander Pöthig, Thorsten Bach

https://doi.org/10.1021/acs.orglett.6b00141

https://doi.org/10.1039/c2sc21832a

Effects of Internal and External Carboxylic Acids on the Reaction Pathway of Organocatalytic 1,4-Addition Reactions between Aldehydes and Nitroolefins
Chem. Sci.. 2013, 4, 1312.
Jörg Duschmalé, Johannes M. Wahl, Markus Wiesner, Helma Wennemers

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