Works matching DE "SULTAMS"
Results: 21
Ring-closure reactions of functionalized vinyl sulfonamides (microreview).
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- Chemistry of Heterocyclic Compounds, 2021, v. 57, n. 6, p. 630, doi. 10.1007/s10593-021-02960-0
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Methods of Sultam Synthesis.
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- Chemistry of Heterocyclic Compounds, 2013, v. 49, n. 1, p. 39, doi. 10.1007/s10593-013-1231-3
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- Article
Synthesis of novel tetra- and pentacyclic benzosultam scaffolds via domino Knoevenagel hetero-Diels-Alder reactions in water.
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- Journal of the Iranian Chemical Society, 2013, v. 10, n. 6, p. 1057, doi. 10.1007/s13738-013-0247-z
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Synthesis of Spirocyclic β‐ and γ‐Sultams by One‐Pot Reductive Cyclization of Cyanoalkylsulfonyl Fluorides.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 47, p. 6530, doi. 10.1002/ejoc.202000351
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- Article
Updating the CSIC Reaction (2003–2020).
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 8, p. 1229, doi. 10.1002/ejoc.202001330
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- Article
Saturated Bicyclic Sultams.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 36, p. 5787, doi. 10.1002/ejoc.202000603
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Sultams: Recent Syntheses and Applications.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 8, p. 933, doi. 10.1002/ejoc.201701491
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- Article
Palladium-Catalyzed Regio- and Chemoselective Reactions of 2-Bromobenzyl Bromides: Expanding the Scope for the Synthesis of Biaryls Fused to a Seven-Membered Sultam.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 36, p. 7885, doi. 10.1002/ejoc.201501032
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A Route to Benzo-Annelated δ-Sultams through Michael Cyclization.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 6, p. 1355, doi. 10.1002/ejoc.201403416
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A Simple and One-Pot Synthesis of β-Sultams by Using the Vilsmeier Reagent.
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- Journal of Heterocyclic Chemistry, 2013, v. 50, n. 2, p. 438, doi. 10.1002/jhet.1630
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Polycarbonate-based benzo- δ-sultam films for high-dose dosimetry in radiation processing.
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- Radiochimica Acta, 2015, v. 103, n. 2, p. 149, doi. 10.1515/ract-2014-2265
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Pd(II)-catalyzed ortho-Hydroxylation and Intramolecular Oxidative C-C Coupling of N-Benzylbenzenesulfonamides.
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- Bulletin of the Korean Chemical Society, 2015, v. 36, n. 2, p. 453, doi. 10.1002/bkcs.10126
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- Article
Enantioselective Access to Spirocyclic Sultams by Chiral Cp<sup>x</sup>-Rhodium(III)-Catalyzed Annulations.
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- Chemistry - A European Journal, 2016, v. 22, n. 7, p. 2270, doi. 10.1002/chem.201504998
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Chemistry of Bridged Lactams: Recent Developments.
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- Molecules, 2019, v. 24, n. 2, p. 274, doi. 10.3390/molecules24020274
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Carbonic Anhydrases inhibitory effects of new benzenesulfonamides synthesized by using superacid chemistry.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2012, v. 27, n. 6, p. 886, doi. 10.3109/14756366.2011.638921
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Generation of α‐Iminyl Radicals from α‐Bromo Cyclic <italic>N</italic>‐Sulfonylimines and Application to Coupling with Various Radical Acceptors Using a Photoredox Catalyst.
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- Chemistry - A European Journal, 2018, v. 24, n. 2, p. 312, doi. 10.1002/chem.201704060
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H<sub>8</sub>‐BINOL‐Derived Chiral η<sup>6</sup>‐Benzene Ligands: New Opportunities for the Ruthenium‐Catalyzed Asymmetric C−H Activation.
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- Angewandte Chemie, 2024, v. 136, n. 31, p. 1, doi. 10.1002/ange.202405782
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Synthesis, Anticancer, Antioxidant, Anti-Inflammatory, Antimicrobial Activities, Molecular Docking, and DFT Studies of Sultams Derived from Saccharin.
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- Molecules, 2022, v. 27, n. 20, p. 7104, doi. 10.3390/molecules27207104
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Continuous Flow Chemistry Synthesis of Spirocyclic Sultams and Isoquinolines through Rhodium‐Catalyzed C−H Activation.
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- European Journal of Organic Chemistry, 2022, v. 2022, n. 47, p. 1, doi. 10.1002/ejoc.202201170
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Oxidation of 3,4-dialkyl substituted isothiazolium salts to 1,1-dioxides.
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- ARKIVOC: Online Journal of Organic Chemistry, 2011, p. 199
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Arene dearomatization through a catalytic N-centered radical cascade reaction.
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- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-16369-4
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- Article