Works matching Acyl cations
Results: 28
N-Methylated Peptide Synthesis via Generation of an Acyl N-Methylimidazolium Cation Accelerated by a Brønsted Acid.
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- Angewandte Chemie, 2020, v. 132, n. 31, p. 13025, doi. 10.1002/ange.202002106
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Ortho CH Acylation of Aryl Iodides by Palladium/Norbornene Catalysis.
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- Angewandte Chemie, 2015, v. 127, n. 43, p. 12855, doi. 10.1002/ange.201506397
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Theoretical Study, Synthesis, and Reactivity of Five-Membered-Ring Acyl Sulfonium Cations.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 28, p. 6125, doi. 10.1002/ejoc.201500749
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Ortho CH Acylation of Aryl Iodides by Palladium/Norbornene Catalysis.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 43, p. 12664, doi. 10.1002/anie.201506397
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Successive Protonation of an N‐Heterocyclic Imine Derived Carbonyl: Superelectrophilic Dication Versus Masked Acylium Ion.
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- Angewandte Chemie, 2018, v. 130, n. 50, p. 16797, doi. 10.1002/ange.201810709
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Facile Smiles-type rearrangement in radical cations of N-acyl arylsulfonamides and analogs.
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- Rapid Communications in Mass Spectrometry: RCM, 2014, v. 28, n. 7, p. 829, doi. 10.1002/rcm.6850
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Solvolysis of aromatic benzoyl chlorides: how is the π-electron stabilization of the aromatic acyl chlorides and acylium cations related to the π-electron delocalization?
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- Journal of Physical Organic Chemistry, 2004, v. 17, n. 8, p. 699, doi. 10.1002/poc.756
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Ab initio Mo calculations on the rearrangements of 7-oxa-2-bicyclo[2.2.1]heptyl cations. The facile migration of acyl group in wagner-meerwein rearrangements.
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- Journal of Physical Organic Chemistry, 1988, v. 1, n. 5, p. 287, doi. 10.1002/poc.610010507
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ALTERNATIVE REVERSE OSMOSIS TO PURIFY LACTIC ACID FROM A FERMENTATION BROTH.
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- Chemical Industry & Chemical Engineering Quarterly, 2018, v. 24, n. 2, p. 179, doi. 10.2298/CICEQ170314030P
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Subcellular potassium and sodium distribution in Saccharomyces cerevisiae wild-type and vacuolar mutants.
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- Biochemical Journal, 2013, v. 454, n. 3, p. 525, doi. 10.1042/BJ20130143
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Functionalized 1′-Substituted Iodoferrocenes and Their Pd-Catalyzed Heck Cross-Coupling Reactions.
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- European Journal of Inorganic Chemistry, 2016, v. 2016, n. 9, p. 1314, doi. 10.1002/ejic.201501451
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N‐Methylated Peptide Synthesis via Generation of an Acyl N‐Methylimidazolium Cation Accelerated by a Brønsted Acid.
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- Angewandte Chemie International Edition, 2020, v. 59, n. 31, p. 12925, doi. 10.1002/anie.202002106
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- Article
Catalytic Activity of the Oxide Catalysts Based on Ni<sub>0.75</sub>Co<sub>2.25</sub>O<sub>4</sub> Modified with Cesium Cations in a Reaction of N<sub>2</sub>O Decomposition.
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- Kinetics & Catalysis, 2017, v. 58, n. 6, p. 793, doi. 10.1134/S002315841705007X
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Synthesis of Ketones with Alkyl Phosphonates and Nitriles as Acyl Cation Equivalent: Application of Dephosphonylation Reaction of β-Functionalized Phosphonate with Hydride.
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- Synthetic Communications, 1997, v. 27, n. 19, p. 3333, doi. 10.1080/00397919708005633
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A New Mechanism for β‐Lactamases: Class D Enzymes Degrade 1β‐Methyl Carbapenems through Lactone Formation.
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- Angewandte Chemie, 2018, v. 130, n. 5, p. 1296, doi. 10.1002/ange.201711308
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Frenkel-Defect-Mediated Chemical Ordering Transition in a Li-Mn-Ni Spinel Oxide.
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- Angewandte Chemie, 2015, v. 127, n. 27, p. 8074, doi. 10.1002/ange.201502320
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Front Cover: Intermediates in Friedel‐Crafts Acylation of Fumaryl Halides (Eur. J. Inorg. Chem. 29/2022).
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- European Journal of Inorganic Chemistry, 2022, v. 2022, n. 29, p. 1, doi. 10.1002/ejic.202200540
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Intermediates in Friedel‐Crafts Acylation of Fumaryl Halides.
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- European Journal of Inorganic Chemistry, 2022, v. 2022, n. 29, p. 1, doi. 10.1002/ejic.202200391
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Acyl Donor Intermediates in N‐Heterocyclic Carbene Catalysis: Acyl Azolium or Azolium Enolate?
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- Angewandte Chemie, 2021, v. 133, n. 9, p. 4557, doi. 10.1002/ange.202010348
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Ring Opening and Closure Reactions of β‐Propiolactone in the Superacids HF/MF<sub>5</sub> (M=Sb, As).
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 48, p. 6628, doi. 10.1002/ejoc.202101351
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2,4,6‐Trimethylpyridine‐Derived Vinylene‐Linked Covalent Organic Frameworks for Confined Catalytic Esterification.
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- Angewandte Chemie, 2022, v. 134, n. 44, p. 1, doi. 10.1002/ange.202210447
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The [(NHC)B(H)C<sub>6</sub>F<sub>5</sub>]<sup>+</sup> Cations and Their [B](H)−CO Borane Carbonyls.
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- Angewandte Chemie, 2020, v. 132, n. 48, p. 21644, doi. 10.1002/ange.202009353
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ETHANOLAMINE AND PENTYL ACETATE INTERACTION CATALYZED BY CATION EXCHANGE RESIN: KINETIC INSIGHT.
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- Journal of Chemistry & Technologies, 2023, v. 31, n. 1, p. 167, doi. 10.15421/jchemtech.v31i1.267433
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Characterization of ionic liquid-based biocatalytic two-phase reaction system for production of biodiesel.
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- AIChE Journal, 2011, v. 57, n. 6, p. 1628, doi. 10.1002/aic.12355
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Third Time is a Charm – Protonating Tricarboxybenzenes.
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- European Journal of Organic Chemistry, 2022, v. 2022, n. 5, p. 1, doi. 10.1002/ejoc.202101488
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Acyl-chain saturation regulates the order of phosphatidylinositol 4,5-bisphosphate nanodomains.
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- Communications Chemistry, 2021, v. 4, n. 1, p. 1, doi. 10.1038/s42004-021-00603-1
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Substituent effects on the formation of sulfonyl cations from sulfonyl chlorides: comparisons of solvolysis kinetic data with calculated gas phase energies.
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- Journal of Physical Organic Chemistry, 2007, v. 20, n. 12, p. 1093, doi. 10.1002/poc.1262
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Identification of genes in the bW/bE regulatory cascade in Ustilago maydis.
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- Molecular Microbiology, 2001, v. 42, n. 4, p. 1047, doi. 10.1046/j.1365-2958.2001.02699.x
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