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Hahn Kim

Researcher at Princeton University

Publications -  31
Citations -  1522

Hahn Kim is an academic researcher from Princeton University. The author has contributed to research in topics: Catalysis & Nucleophile. The author has an hindex of 13, co-authored 31 publications receiving 1005 citations. Previous affiliations of Hahn Kim include Seoul National University.

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Enantioselective Organo-SOMO Catalysis : The α-Vinylation of Aldehydes

TL;DR: The first enantioselective organocatalytic α-vinylation of aldehydes has been accomplished in this paper, where the SOMO-activated species undergo direct coupling with readily available potassium organotrifluoroborate salts to yield enantioenriched αvinyl aldehyde.
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Human SHMT inhibitors reveal defective glycine import as a targetable metabolic vulnerability of diffuse large B-cell lymphoma

TL;DR: It is shown genetically that dual SHMT1/2 knockout blocks HCT-116 colon cancer tumor xenograft formation and defective glycine import is a targetable metabolic deficiency of DLBCL.
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Flavonoids suppress Pseudomonas aeruginosa virulence through allosteric inhibition of quorum-sensing Receptors

TL;DR: This work demonstrates that flavonoids specifically inhibit quorum sensing via antagonism of the autoinducer-binding receptors, LasR and RhlR, and confirms their potential as anti-infectives that do not function by traditional bacteriocidal or bacteriostatic mechanisms.
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A Dual-Mechanism Antibiotic Kills Gram-Negative Bacteria and Avoids Drug Resistance.

TL;DR: A compound is characterized that kills both Gram-negative and Gram-positive bacteria through a unique dual-targeting mechanism of action (MoA) with undetectably low resistance frequencies, and suggests that combining multiple MoAs onto a single chemical scaffold may be an underappreciated approach to targeting challenging bacterial pathogens.
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Stereoselective palladium-catalyzed O-glycosylation using glycals

TL;DR: The combination of the glycosylation and subsequent functionalization provides a novel entry to saccharides which are otherwise difficult to prepare and should make this method a useful tool in synthetic carbohydrate chemistry.