Search Results - "Poremba, Kelsey E"

Nickel-Catalyzed Enantioselective Reductive Cross-Coupling Reactions by Poremba, Kelsey E, Dibrell, Sara E, Reisman, Sarah E

“…Nickel-catalyzed reductive cross-coupling reactions have emerged as powerful methods to join two electrophiles. These reactions have proven particularly useful…”
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Nickel-Catalyzed Enantioselective Cross-Coupling of N‑Hydroxyphthalimide Esters with Vinyl Bromides by Suzuki, Naoyuki, Hofstra, Julie L, Poremba, Kelsey E, Reisman, Sarah E

“…An enantioselective Ni-catalyzed cross-coupling of N-hydroxyphthalimide esters with vinyl bromides is reported. The reaction proceeds under mild conditions and…”
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Nickel-Catalyzed Asymmetric Reductive Cross-Coupling To Access 1,1-Diarylalkanes by Poremba, Kelsey E, Kadunce, Nathaniel T, Suzuki, Naoyuki, Cherney, Alan H, Reisman, Sarah E

“…An asymmetric Ni-catalyzed reductive cross-coupling of (hetero)­aryl iodides and benzylic chlorides has been developed to prepare enantioenriched…”
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Nickel‐Catalyzed Conversion of Enol Triflates into Alkenyl Halides by Hofstra, Julie L., Poremba, Kelsey E., Shimozono, Alex M., Reisman, Sarah E.

“…A Ni‐catalyzed halogenation of enol triflates was developed and it enables the synthesis of a broad range of alkenyl iodides, bromides, and chlorides under…”
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Nickel-catalyzed asymmetric reductive cross-coupling of α-chloroesters with (hetero)aryl iodides by DeLano, Travis J, Dibrell, Sara E, Lacker, Caitlin R, Pancoast, Adam R, Poremba, Kelsey E, Cleary, Leah, Sigman, Matthew S, Reisman, Sarah E

“…An asymmetric reductive cross-coupling of α-chloroesters and (hetero)aryl iodides is reported. This nickel-catalyzed reaction proceeds with a chiral BiOX…”
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Structure-Guided Discovery of Aminoquinazolines as Brain-Penetrant and Selective LRRK2 Inhibitors by Keylor, Mitchell H, Gulati, Anmol, Kattar, Solomon D, Johnson, Rebecca E, Chau, Ryan W, Margrey, Kaila A, Ardolino, Michael J, Zarate, Cayetana, Poremba, Kelsey E, Simov, Vladimir, Morriello, Gregori J, Acton, John J, Pio, Barbara, Yan, Xin, Palte, Rachel L, McMinn, Spencer E, Nogle, Lisa, Lesburg, Charles A, Adpressa, Donovon, Lin, Shishi, Neelamkavil, Santhosh, Liu, Ping, Su, Jing, Hegde, Laxminarayan G, Woodhouse, Janice D, Faltus, Robert, Xiong, Tina, Ciaccio, Paul J, Piesvaux, Jennifer, Otte, Karin M, Wood, Harold B, Kennedy, Matthew E, Bennett, David Jonathan, DiMauro, Erin F, Fell, Matthew J, Fuller, Peter H

“…The leucine-rich repeat kinase 2 (LRRK2) protein has been genetically and functionally linked to Parkinson’s disease (PD), a disabling and progressive…”
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Correction to “Nickel-Catalyzed Asymmetric Reductive Cross-Coupling To Access 1,1-Diarylalkanes” by Poremba, Kelsey E, Kadunce, Nathaniel T, Suzuki, Naoyuki, Cherney, Alan H, Reisman, Sarah E

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Synthesis of α-chiral-β,γ-unsaturated carboxylic acid derivatives using chiral auxiliaries by Poremba, Kelsey E., Lee, Victoria A., Sculimbrene, Bianca R.

“…We report an efficient and reliable method for the synthesis of α-chiral-β,γ-unsaturated carboxylic acid derivatives using chiral auxiliaries and vinylacetic…”
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Nickel‐Catalyzed Conversion of Enol Triflates into Alkenyl Halides by Hofstra, Julie L., Poremba, Kelsey E., Shimozono, Alex M., Reisman, Sarah E.

“…A Ni‐catalyzed halogenation of enol triflates was developed and it enables the synthesis of a broad range of alkenyl iodides, bromides, and chlorides under…”
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Ni-Catalyzed Conversion of Enol Triflates to Alkenyl Halides by Hofstra, Julie L., Poremba, Kelsey E., Shimozono, Alex M., Reisman, Sarah E.

“…A Ni-catalyzed halogenation of enol triflates was developed that enables the synthesis of a broad range of alkenyl iodides, bromides, and chlorides under mild…”
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