Sven Roediger
@sevenroediger.bsky.social
Postdoc in the Doyle Group at UCLA
Happy to share my postdoc work: We developed an ML-based python tool for the selection of reaction scopes that balances the performance and diversity of the selected substrates, allowing benchmarked and standardized scope selection.
(1/n)
t.co/hCsNslOle0
(1/n)
t.co/hCsNslOle0
December 23, 2025 at 8:40 AM
Happy to share my postdoc work: We developed an ML-based python tool for the selection of reaction scopes that balances the performance and diversity of the selected substrates, allowing benchmarked and standardized scope selection.
(1/n)
t.co/hCsNslOle0
(1/n)
t.co/hCsNslOle0
Reposted by Sven Roediger
It’s finally happening!🎉 The Reisenbauer Lab will open in February at ISTA (www.reisenbauerlab.com
).
We’re starting to build our team and are looking for enthusiastic scientists to join us.
I feel deeply grateful to my mentors, colleagues, and family for all their support. Excited for what’s next!
).
We’re starting to build our team and are looking for enthusiastic scientists to join us.
I feel deeply grateful to my mentors, colleagues, and family for all their support. Excited for what’s next!
Home | Reisenbauer Lab
The Reisenbauer Lab is a research group in biocatalysis and enzyme engineering at the IST Austria.
www.reisenbauerlab.com
October 24, 2025 at 11:43 AM
It’s finally happening!🎉 The Reisenbauer Lab will open in February at ISTA (www.reisenbauerlab.com
).
We’re starting to build our team and are looking for enthusiastic scientists to join us.
I feel deeply grateful to my mentors, colleagues, and family for all their support. Excited for what’s next!
).
We’re starting to build our team and are looking for enthusiastic scientists to join us.
I feel deeply grateful to my mentors, colleagues, and family for all their support. Excited for what’s next!
Reposted by Sven Roediger
Congrats to @mixalhsmpogdos.bsky.social, @sevenroediger.bsky.social, @fruepp.bsky.social, Nathalie, Patrick, Fabio and Jan on this epic study of C-N red. elim. in @jacs.acspublications.org - using causal inference, organometallics, electrochemistry, kinetics and DFT. pubs.acs.org/doi/full/10....
October 14, 2025 at 9:50 AM
Congrats to @mixalhsmpogdos.bsky.social, @sevenroediger.bsky.social, @fruepp.bsky.social, Nathalie, Patrick, Fabio and Jan on this epic study of C-N red. elim. in @jacs.acspublications.org - using causal inference, organometallics, electrochemistry, kinetics and DFT. pubs.acs.org/doi/full/10....
Reposted by Sven Roediger
Congrats to @mixalhsmpogdos.bsky.social, @sevenroediger.bsky.social, @fruepp.bsky.social, Patrick, Nathalie, Fabio on this epic study of the factors governing reductive elimination - using causal inference, organometallics, electrochemistry, kinetics and DFT
@chemrxiv.bsky.social go.shr.lc/4j8O5MM
@chemrxiv.bsky.social go.shr.lc/4j8O5MM
Metal Electronics Mediate Steric and Coordination Number Effects on Palladium (II) C–X Reductive Elimination
Reductive elimination is the key bond-forming elementary step in many transition metal catalyzed reactions relevant to the synthesis of pharmaceuticals, materials and fine chemicals. Metal electronics...
go.shr.lc
April 11, 2025 at 8:24 PM
Congrats to @mixalhsmpogdos.bsky.social, @sevenroediger.bsky.social, @fruepp.bsky.social, Patrick, Nathalie, Fabio on this epic study of the factors governing reductive elimination - using causal inference, organometallics, electrochemistry, kinetics and DFT
@chemrxiv.bsky.social go.shr.lc/4j8O5MM
@chemrxiv.bsky.social go.shr.lc/4j8O5MM
Reposted by Sven Roediger
Many congrats to Emilien Le Saux for this new publication in @jacs.acspublications.org describing a catalytic approach to Transfer Iodination from Aryl Iodides to Nonactivated C(sp3)–H Bonds.
pubs.acs.org/doi/10.1021/...
pubs.acs.org/doi/10.1021/...
Palladium-Catalyzed Transfer Iodination from Aryl Iodides to Nonactivated C(sp3)–H Bonds
We report a new strategy for the catalytic iodination of nonactivated C(sp3)–H bonds. The method merges the concepts of shuttle and light-enabled palladium catalysis to employ aryl iodides as both hyd...
pubs.acs.org
April 8, 2025 at 1:03 PM
Many congrats to Emilien Le Saux for this new publication in @jacs.acspublications.org describing a catalytic approach to Transfer Iodination from Aryl Iodides to Nonactivated C(sp3)–H Bonds.
pubs.acs.org/doi/10.1021/...
pubs.acs.org/doi/10.1021/...
Reposted by Sven Roediger
Many Congrats to @ybraegger.bsky.social,
Ann-Sophie Paschke, Nima Nasiri, Bence Botlik
and Francesco Felician for this masterpiece! Oxidative amination by nitrogen atom insertion into carbon-carbon double bonds in Science, @ethzurich.bsky.social.
www.science.org/doi/10.1126/...
Ann-Sophie Paschke, Nima Nasiri, Bence Botlik
and Francesco Felician for this masterpiece! Oxidative amination by nitrogen atom insertion into carbon-carbon double bonds in Science, @ethzurich.bsky.social.
www.science.org/doi/10.1126/...
Oxidative amination by nitrogen atom insertion into carbon-carbon double bonds
The synthesis of nitrogen-containing molecules through carbon–nitrogen (C–N) bond formation is critical for the discovery and preparation of medicines, agrochemicals, and materials. Here, we report th...
www.science.org
March 7, 2025 at 8:50 AM
Many Congrats to @ybraegger.bsky.social,
Ann-Sophie Paschke, Nima Nasiri, Bence Botlik
and Francesco Felician for this masterpiece! Oxidative amination by nitrogen atom insertion into carbon-carbon double bonds in Science, @ethzurich.bsky.social.
www.science.org/doi/10.1126/...
Ann-Sophie Paschke, Nima Nasiri, Bence Botlik
and Francesco Felician for this masterpiece! Oxidative amination by nitrogen atom insertion into carbon-carbon double bonds in Science, @ethzurich.bsky.social.
www.science.org/doi/10.1126/...
Reposted by Sven Roediger
Also in @science.org for chemsky this week, we have two methods of turning olefins into nitriles, respectively from Bill Morandi's group and Ning Jiao's group 🧪
www.science.org/doi/10.1126/...
www.science.org/doi/10.1126/...
Oxidative amination by nitrogen atom insertion into carbon-carbon double bonds
The synthesis of nitrogen-containing molecules through carbon–nitrogen (C–N) bond formation is critical for the discovery and preparation of medicines, agrochemicals, and materials. Here, we report th...
www.science.org
March 6, 2025 at 8:15 PM
Also in @science.org for chemsky this week, we have two methods of turning olefins into nitriles, respectively from Bill Morandi's group and Ning Jiao's group 🧪
www.science.org/doi/10.1126/...
www.science.org/doi/10.1126/...
Reposted by Sven Roediger
Congrats to @sevenroediger.bsky.social and team as well as Tanner Jankins and team for having their papers highlighted this month in OPRD items of interest to process chem 😀 pubs.acs.org/doi/10.1021/...
Some Items of Interest to Process R&D Chemists and Engineers
pubs.acs.org
February 20, 2025 at 8:26 PM
Congrats to @sevenroediger.bsky.social and team as well as Tanner Jankins and team for having their papers highlighted this month in OPRD items of interest to process chem 😀 pubs.acs.org/doi/10.1021/...
Reposted by Sven Roediger
New radical cross-coupling using phosphonium salts and HMDS anion as the electron donor:
www.nature.com/articles/s41...
I watched Sven lead this work experimentally and computationally and was very impressed - very rare for someone to be so adept at both. Great to see his hard work pay off.
www.nature.com/articles/s41...
I watched Sven lead this work experimentally and computationally and was very impressed - very rare for someone to be so adept at both. Great to see his hard work pay off.
Coupling of unactivated alkyl electrophiles using frustrated ion pairs - Nature
A transition-metal-free platform enables the formation of challenging C(sp3)–C(sp3) bonds in organic compounds via single-electron transfer, facilitating the coupling of functionalized fragments and e...
www.nature.com
November 23, 2024 at 9:02 AM
New radical cross-coupling using phosphonium salts and HMDS anion as the electron donor:
www.nature.com/articles/s41...
I watched Sven lead this work experimentally and computationally and was very impressed - very rare for someone to be so adept at both. Great to see his hard work pay off.
www.nature.com/articles/s41...
I watched Sven lead this work experimentally and computationally and was very impressed - very rare for someone to be so adept at both. Great to see his hard work pay off.