mesityl (2,4,6-trimethylphenyl) (Mes)

(1) Eight-membered-ring diaminocarbenes bearing naphthalene moiety in the backbone: DFT studies, synthesis of amidinium salts, generation of free carbene, metal complexes, and solvent-free copper catalyzed azide-alkyne cycloaddition (CuAAC) reaction (Dalton Trans. 2017, 46, 4331−4345; 10.1039/C6DT04484K) Mes, Dipp, AAC, Cat, Cu, CA, Het, SS, NpH, CuAAC, 8MR, NHC

maximal electroshock seizure (MES)

(1) Identification of CNS-Penetrant Aryl Sulfonamides as Isoform-Selective NaV1.6 Inhibitors with Efficacy in Mouse Models of Epilepsy (J. Med. Chem. 2019, 62, 9618−9641; 10.1021/acs.jmedchem.9b01032) PXR, DC, d.c., lb, Na, 57-13-6, MES

(2) Evaluation of Selective 5-HT2C Agonists in Acute Seizure Models (ACS Chem. Neurosci. 2019, 10, 3284−3295; 10.1021/acschemneuro.8b00739) EL, MES

(3) Searching for New Leads To Treat Epilepsy: Target-Based Virtual Screening for the Discovery of Anticonvulsant Agents (J. Chem. Inf. Model. 2018, 58, 1331−1342; 10.1021/acs.jcim.7b00721) GP, EL, VAL, CIP, MES

(4) Design and Synthesis of Selurampanel, a Novel Orally Active and Competitive AMPA Receptor Antagonist (ChemMedChem 2017, 12, 197−201; 10.1002/cmdc.201600467) EL, 79-09-4, Me, MES, iPr, i-Pr

(5) Design, synthesis and anticonvulsant-analgesic activity of new N-[(phenoxy)alkyl]- and N-[(phenoxy)ethoxyethyl]aminoalkanols (Med. Chem. Commun. 2017, 8, 220−238; 10.1039/C6MD00537C) MES, PTZ

2-mercaptoethanesulfonic acid (MES)

(1) Identification of an Enzyme Catalyzing the Conversion of Sulfoacetaldehyde to 2-Mercaptoethanesulfonic Acid in Methanogens (Biochemistry 2019, 58, 1958−1962; 10.1021/acs.biochem.9b00176) MES, MESNA, MESA, S, HCys, Hcy, FG, CH4

(2) Identification and Biosynthesis of 1-Mercaptoethanesulfonic Acid (1-MES), an Analogue of Coenzyme M, Found Widely in the Methanogenic Archaea (Biochemistry 2017, 56, 6137−6144; 10.1021/acs.biochem.7b00971) MES, MESNA, MESA, R, UV, VSA

(3) A Facile N-Mercaptoethoxyglycinamide (MEGA) Linker Approach to Peptide Thioesterification and Cyclization (J. Am. Chem. Soc. 2017, 139, 3946−3949; 10.1021/jacs.6b13271) MES, MESNA, MESA, AA, E, FG, El

(4) Electrochemical determination of fisetin using gold electrodes modified with thiol self-assembled monolayers (J. Electroanal. Chem. 2017, 790, 1−10; 10.1016/j.jelechem.2017.02.030) PB, CA, PBS, EIS, MES, MESNA, MESA, IS, Au, EC, ML, SWV, SAM

(5) Development of functionalized quantum dot modified poly(vinyl alcohol) membranes for fuel cell applications (RSC Adv. 2016, 6, 47536−47544; 10.1039/C6RA03365B) MES, MESNA, MESA, L, FC, PVOH, PVA, MPA, 3MA, QD

microstructured electrode scaffold (MES)

(1) Ionic Conductivity over Metal/Water Interfaces in Ionomer-Free Fuel Cell Electrodes (ChemElectroChem 2019, 6, 2659−2666; 10.1002/celc.201900124) PEM, PEMFC, CV, CV, Au, H, EC, Pt, FC, O, CL, EDL, MEA, RH, C, ORR, MES

maximally entangled state (MES)

(1) Optimal control of orientation and entanglement for two dipole-dipole coupled quantum planar rotors (Phys. Chem. Chem. Phys. 2018, 20, 13008−13029; 10.1039/C8CP00231B) DD, MOS, MES

4-morpholineethanesulfonic acid (MES)
2-(methacryloyloxy)ehtyl succinate (MES)
modulation excitation spectroscopy (MES)

(1) Design of an optimized DRIFT cell/microreactor for spectrokinetic investigations of surface reaction mechanisms (Mol. Catal. 2020, 481, 100628−; https://doi.org/10.1016/j.mcat.2018.07.003) det., DRIFTS, TRIR, IS, TR, FT, oxidn., DRIFT, expt., PSD, MES

(2) Probing the Active Sites of MoS2 Based Hydrotreating Catalysts Using Modulation Excitation Spectroscopy (ACS Catal. 2019, 9, 2568−2579; 10.1021/acscatal.8b04778) Pr, H, O, S, DFT, POX, MES, C

(3) Dominant Role of Entropy in Stabilizing Sugar Isomerization Transition States within Hydrophobic Zeolite Pores (J. Am. Chem. Soc. 2018, 140, 14244−14266; 10.1021/jacs.8b08336) TOR, ATR, Glu, H, TS, LA, FEL, GFE, Glc, RC, ZL, HB, LAS, Glu, Glu, MES

(4) Hydrogenation of Acetophenone on Pd/Silica–Alumina Catalysts with Tunable Acidity: Mechanistic Insight by In Situ ATR-IR Spectroscopy (ACS Catal. 2018, 8, 6594−6600; 10.1021/acscatal.8b00169) 98-86-2, St, H, EB, PSD, MES, PEA

(5) Molecular recognition of an acyl-enzyme intermediate on the lipase B from Candida antarctica (Catal. Sci. Technol. 2017, 7, 1953−1964; 10.1039/C7CY00245A) TR, KP, Ser, S, PSD, MES

molecular emission spectrometry (MES)

(1) Determination of nitrate and ammonium ions in water samples by atmospheric pressure glow discharge microplasma molecular emission spectrometry coupled with chemical vapour generation (J. Anal. At. Spectrom. 2018, 33, 2153−2159; 10.1039/C8JA00287H) CCD, Ar, CRM, IF, em, AP, am, DL, RM, APGD, MES, CVG

mesulergine (Mes)
methyl ester sulfonate (MES)

(1) Development and evaluation of a novel seawater-based viscoelastic fracturing fluid system (J. Pet. Sci. Eng. 2019, 183, 106408−; https://doi.org/10.1016/j.petrol.2019.106408) MES

(2) Micellar Effects on the Hydrolysis Reaction of an Anionic Surfactant in Aqueous Solution (Langmuir 2018, 34, 13979−13992; 10.1021/acs.langmuir.8b03451) Ca, MES, CMC, IF, FL, H, K, Na, Me

(3) Adsorption of Methyl Ester Sulfonate at the Air–Water Interface: Can Limitations in the Application of the Gibbs Equation be Overcome by Computer Purification? (Langmuir 2017, 33, 9944−9953; 10.1021/acs.langmuir.7b02725) MES, CMC, Na, PFO, AWI, AOT, Me

microbial electrochemical system (MES)

(1) Exoelectrogenic Anaerobic Granular Sludge for Simultaneous Electricity Generation and Wastewater Treatment (Environ. Sci. Technol. 2019, 53, 12130−12140; 10.1021/acs.est.9b03395) MFC, C, EC, FC, OC, MES, AGS

(2) Anaerobic electrogenic oxidation of toluene in a continuous-flow bioelectrochemical reactor: process performance, microbial community analysis, and biodegradation pathways (Environ. Sci.: Water Res. Technol. 2018, 4, 2136−2145; 10.1039/C8EW00666K) EC, HC, PhMe, CE, fma, TolH, MES

February 17, 2020
February 17, 2020
Org. Lett. 2020, 22 (3), 1124−1129.
February 14, 2020
February 14, 2020
Angew. Chem. Int. Ed. 2020, 59 (8), 3147−3150.
February 13, 2020
February 13, 2020
Angew. Chem. Int. Ed. 2020, 59 (8), 3063−3068.
February 12, 2020
February 12, 2020
Org. Lett. 2020, 22 (3), 768−771.
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J. Am. Chem. Soc. 2019, 141 (14), 2298−2301.
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(c) Nanoniele, 2003-