L
Leslie T. Gelbaum
Researcher at Georgia Institute of Technology
Publications - 61
Citations - 1116
Leslie T. Gelbaum is an academic researcher from Georgia Institute of Technology. The author has contributed to research in topics: Pyrrolizidine & Formic acid. The author has an hindex of 19, co-authored 61 publications receiving 1053 citations.
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Journal ArticleDOI
Cuticular hydrocarbons ofReticulitermes virginicus (Banks) and their role as potential species- and caste-recognition cues.
Ralph W. Howard,C. A. McDaniel,Dennis R. Nelson,Gary J. Blomquist,Leslie T. Gelbaum,Leon H. Zalkow +5 more
TL;DR: A bioassay was developed to test the species-recognition hypothesis and the experimental results supporting the hypothesis suggest that cuticular hydrocarbons might serve as species- and caste- Recognition cues.
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1H NMR investigation of thermally triggered insulin release from poly(N-isopropylacrylamide) microgels.
TL;DR: Investigations of insulin release from thermoresponsive microgels using variable temperature (1)H NMR studies suggest that the swelling loading method results in enhanced entrapment of the peptide versus equilibrium partitioning.
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A dinuclear silver hydride and an umpolung reaction of CO2
Brandon K. Tate,Chelsea M. Wyss,John Bacsa,Kelly A. Kluge,Leslie T. Gelbaum,Joseph P. Sadighi +5 more
TL;DR: In this article, a triangular [Ag2H]+ core is stabilised by the N-heterocyclic carbene (NHC) ligand 1,3-bis(2,6-diisopropylphenyl)imidazolin-2-ylidene (SIDipp).
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Reversible Ionic Liquid Stabilized Carbamic Acids: A Pathway Toward Enhanced CO2 Capture
Jackson R. Switzer,Amy L. Ethier,Kyle M. Flack,Elizabeth J. Biddinger,Leslie T. Gelbaum,Pamela Pollet,Charles A. Eckert,Charles L. Liotta +7 more
TL;DR: In this paper, nonaqueous silylamines can be used to efficiently and reversibly capture and release CO2 via the formation of reversible ionic liquids, achieving a 3:2 amine to CO2 mole ratio.
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Cascade synthesis of benzofuran derivatives via laccase oxidation–Michael addition
TL;DR: The cascade synthesis of benzofuran derivatives was conducted from the reaction of catechols and 1,3-dicarbonyl compounds via oxidation–Michael addition in the presence of laccase and Sc(OTf)3/SDS, and this reaction system showed recyclability.