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202 results

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Page 1
Photoactivatable Odorants for Chemosensory Research.
Gore S, Ukhanov K, Herbivo C, Asad N, Bobkov YV, Martens JR, Dore TM. Gore S, et al. ACS Chem Biol. 2020 Sep 18;15(9):2516-2528. doi: 10.1021/acschembio.0c00541. Epub 2020 Aug 31. ACS Chem Biol. 2020. PMID: 32865973
Chemically distinct ligands eugenol, benzaldehyde, 2-phenethylamine, ethanethiol, butane-1-thiol, and 2,2-dimethylethane-1-thiol were modified by covalently attaching the photoremovable protecting group (8-cyano-7-hydroxyquinolin-2-yl)methyl (CyHQ). ...
Chemically distinct ligands eugenol, benzaldehyde, 2-phenethylamine, ethanethiol, butane-1-thiol, and 2,2-dimethylethan …
Engineering volatile thiol formation in yeast.
Graf FMR, Buchhaupt M. Graf FMR, et al. J Appl Microbiol. 2023 Feb 16;134(2):lxac078. doi: 10.1093/jambio/lxac078. J Appl Microbiol. 2023. PMID: 36626784
Well-characterized thiols such as 2-methyl-2-butanethiol, 3-mercapto-3-methylbutan-1-ol, and 8-mercapto-p-menthan-3-one, as well as several so far undescribed thiol compounds could be synthesized. ...
Well-characterized thiols such as 2-methyl-2-butanethiol, 3-mercapto-3-methylbutan-1-ol, and 8-mercapto-p-menthan-3-one, as well as s …
Conformations and Low-Frequency Intramolecular Motions of 1-Butanol, 1-Butanethiol, Iso-butanol, and Iso-butanethiol Investigated by Fourier Transform Microwave Spectroscopy Combined with Quantum Chemical Calculations.
Kawashima Y, Tanaka Y, Uzuyama T, Hirota E. Kawashima Y, et al. J Phys Chem A. 2021 Feb 11;125(5):1166-1183. doi: 10.1021/acs.jpca.0c09687. Epub 2021 Jan 27. J Phys Chem A. 2021. PMID: 33502865
The rotational spectra of 1-butanol (1-BuOH), 1-butanethiol (1-BuSH), 2-methyl-1-propanol (iso-BuOH), and 2-methyl-1-propanethiol (iso-BuSH) were measured by Fourier transform microwave spectroscopy in the frequency region from 3.7 up to 25 GHz. ...
The rotational spectra of 1-butanol (1-BuOH), 1-butanethiol (1-BuSH), 2-methyl-1-propanol (iso-BuOH), and 2-methyl-1-propaneth …
From Molecules to Surfaces: Radical-Based Mechanisms of Si-S and Si-Se Bond Formation on Silicon.
Buriak JM, Sikder MD. Buriak JM, et al. J Am Chem Soc. 2015 Aug 5;137(30):9730-8. doi: 10.1021/jacs.5b05738. Epub 2015 Jul 22. J Am Chem Soc. 2015. PMID: 26161463 Free article.
Using a diazonium-based radical initiator, which induces formation of surface silicon radicals, a group of organochalcogenides were screened for reactivity at room temperature, including di-n-butyl disulfide, diphenyl disulfide, diphenyl diselenide, di-n-butyl sulfide, diphenyl s …
Using a diazonium-based radical initiator, which induces formation of surface silicon radicals, a group of organochalcogenides were screened …
Molecular Dynamics Study of Hydrophilic Sphalerite (110) Surface as Modified by Normal and Branched Butylthiols.
Anvari MH, Liu Q, Xu Z, Choi P. Anvari MH, et al. Langmuir. 2018 Mar 13;34(10):3363-3373. doi: 10.1021/acs.langmuir.7b04303. Epub 2018 Mar 1. Langmuir. 2018. PMID: 29451389
Molecular dynamics simulation was used to study the wettability of the hydrophilic sphalerite (110) surface chemically modified by butylthiols made up of normal and branched alkyl tails, referred to as n-butylthiol and i-butylthiol hereafter, at different ads …
Molecular dynamics simulation was used to study the wettability of the hydrophilic sphalerite (110) surface chemically modified by butylthio …
NEXAFS study of 1-butanethiol adsorbed on Cu(111) and square root of 7 x square root of 7 R19.1 degrees S/Cu(111).
Yang YW, Venkatesh S, Fan LJ, Dann TE, Lai LJ. Yang YW, et al. J Synchrotron Radiat. 2001 Jul 1;8(4):1121-3. doi: 10.1107/s0909049500016782. J Synchrotron Radiat. 2001. PMID: 11486365
The adsorption of 1-butanethiol on Cu(111) and square root of 7 x square root of 7 R19.1 degrees S/Cu(111) surfaces has been studied by S K-edge near edge X-ray absorption fine structure (NEXAFS) spectroscopy and thermal desorption spectroscopy. ...In contrast, on s …
The adsorption of 1-butanethiol on Cu(111) and square root of 7 x square root of 7 R19.1 degrees S/Cu(111) surfaces has been s …
Odorant Monitoring in Natural Gas Pipelines Using Ultraviolet-Visible Spectroscopy.
Galassi R, Contini C, Pucci M, Gambi E, Manca G. Galassi R, et al. Appl Spectrosc. 2021 Feb;75(2):168-177. doi: 10.1177/0003702820960737. Epub 2020 Oct 8. Appl Spectrosc. 2021. PMID: 32880187
Currently, the detection of the most common odorants (THT = tetrahydrothiophane; TBM = tertiary butyl mercaptan) added to natural gas streams in pipelines is made in situ by using portable gas chromatography apparatuses. ...The absorption maxima of thiophane and ter …
Currently, the detection of the most common odorants (THT = tetrahydrothiophane; TBM = tertiary butyl mercaptan) added to natu …
Synthesis of Four-Disulfide Insulin Analogs via Sequential Disulfide Bond Formation.
Wu F, Mayer JP, Gelfanov VM, Liu F, DiMarchi RD. Wu F, et al. J Org Chem. 2017 Apr 7;82(7):3506-3512. doi: 10.1021/acs.joc.6b03078. Epub 2017 Mar 27. J Org Chem. 2017. PMID: 28319665
Cysteine protection consisted of tert-butylthiol (StBu), thiol-trimethoxyphenyl (STmp), trityl (Trt), 4-methoxytrityl (Mmt), S-acetamidomethyl (Acm), and tert-butyl (tBu). ...
Cysteine protection consisted of tert-butylthiol (StBu), thiol-trimethoxyphenyl (STmp), trityl (Trt), 4-methoxytrityl (Mmt), S-acetam …
Thiol Metabolism and Volatile Metabolome of Clostridioides difficile.
Biwer P, Neumann-Schaal M, Henke P, Jahn D, Schulz S. Biwer P, et al. Front Microbiol. 2022 Jun 16;13:864587. doi: 10.3389/fmicb.2022.864587. eCollection 2022. Front Microbiol. 2022. PMID: 35783419 Free PMC article.
Major components were identified to be 2-methyl-1-propanol, 2-methyl-1-propanethiol, 2-methyl-1-butanethiol, 4-methyl-1-pentanethiol, and as well as their disulfides. Structurally identified were 64 sulfur containing volatiles. ...
Major components were identified to be 2-methyl-1-propanol, 2-methyl-1-propanethiol, 2-methyl-1-butanethiol, 4-methyl-1-pentan …
Alkanethiol-functionalized organosilicon monoliths for nano-reversed-phase liquid chromatography.
Demir C, Kip Ç, Tuncel A. Demir C, et al. Electrophoresis. 2018 Nov;39(22):2919-2928. doi: 10.1002/elps.201800280. Epub 2018 Sep 21. Electrophoresis. 2018. PMID: 30194741
The use of thiol-ene chemistry in the presence of a main monomer with a series of methacrylate functionality (i.e., methacrylate substituted polyhedral oligomeric silsesquioxane) allowed the synthesis of organosilicon monoliths with high cross-linking density and carrying hydroph …
The use of thiol-ene chemistry in the presence of a main monomer with a series of methacrylate functionality (i.e., methacrylate substituted …
202 results