Works matching IS 00093122 AND DT 2020 AND VI 56 AND IP 7
Results: 27
Interaction of 1,3λ<sup>4</sup>δ<sup>2</sup>,2,4-benzodithiadiazines with neutral and charged S-electrophiles: SCl<sub>2</sub>, C<sub>6</sub>F<sub>5</sub>SCl, and NS<sub>2</sub><sup>+</sup>.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 7, p. 968, doi. 10.1007/s10593-020-02760-y
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Reactions of quinoline-2(6,8)-carbaldehydes with arenes by the action of various Brønsted or Lewis acids: synthesis of diarylmethylquinolines.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 7, p. 964, doi. 10.1007/s10593-020-02759-5
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Electrophilic Reactions of 5-Aryltetrazoles: Synthesis of Isomeric 2-(Adamantan-1-Yl)-5-Nitrophenyl-2H-Tetrazoles and their Derivatives.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 7, p. 961, doi. 10.1007/s10593-020-02758-6
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Synthesis of 3-Fluoropyrazolo[1,5-A]Pyridines by Fluorination of Methyl Pyrazolo[1,5-A]Pyridine-3-Carboxylates.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 7, p. 957, doi. 10.1007/s10593-020-02757-7
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Cyclization of 1-Aryl-5-Phenylpent-4-en-2-yn-1-Ones to 2,3-Dihydropyran-2-Ones in Trifluoromethanesulfonic Acid.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 7, p. 953, doi. 10.1007/s10593-020-02756-8
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One-pot propargylation and Claisen-type rearrangement for natural lignans matairesinol and α-conidendrin.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 7, p. 949, doi. 10.1007/s10593-020-02755-9
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Synthesis of antiaromatic thiazinoindolizines based on electrophilic cyclizations of indolizine-5-thione.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 7, p. 942, doi. 10.1007/s10593-020-02754-w
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Synthesis of 1,3-Oxazine Derivatives Based on (–)-Isopulegol using the Ritter Reaction and Study of their Analgesic Activity.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 7, p. 936, doi. 10.1007/s10593-020-02753-x
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Iodine Acetate as a Mild Selective Agent for the Wagner–Meerwein Rearrangement in 3a,6-Epoxyisoindoles.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 7, p. 930, doi. 10.1007/s10593-020-02752-y
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Electrophilic reactions as methods of modification of pyrrolobenzimidazolones and pyrroloquinazolinones.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 7, p. 923, doi. 10.1007/s10593-020-02751-z
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N-Propargylation and Copper(I)-Catalyzed Azide-Alkyne Cycloaddition as a Convenient Strategy for Directed Post-Synthetic Modification of 4-Oxo-1,4-Dihydrocinnoline Derivatives.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 7, p. 915, doi. 10.1007/s10593-020-02750-0
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Influence of Positive Charge on the NMR Parameters of Mono- and Diprotonated Forms of 4-Dimethylaminopyridine.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 7, p. 892, doi. 10.1007/s10593-020-02749-7
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Transformations of 1-phenethyl-1,2,3,6-tetrahydropyridines in the presence of trifluoromethanesulfonic acid.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 7, p. 909, doi. 10.1007/s10593-020-02748-8
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Transformations of 1-[2-(Adamantan-1-Yl)-2-Hydroxyethyl]-1,2,3,6-Tetrahydropyridines by the Action of Trifluoromethanesulfonic Acid.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 7, p. 898, doi. 10.1007/s10593-020-02747-9
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Synthesis of novel macrocyclic and heterocyclic taurine derivatives based on the reaction of sodium 2-[(4,4-diethoxybutyl)amino]ethanesulfonate with phenols.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 7, p. 888, doi. 10.1007/s10593-020-02746-w
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Acid-catalyzed rearrangement of 1-acyl-2-azabuta-1,3-dienes to 4-pyrrolin-2-ones.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 7, p. 881, doi. 10.1007/s10593-020-02745-x
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Magnesium acetate – an effective electrophilic activator of the carbonyl group in transesterification of dialkylaziridine dicarboxylates.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 7, p. 875, doi. 10.1007/s10593-020-02744-y
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Synthesis of Fluorinated Octahydro-2H-Chromenes in the Presence of the BF<sub>3</sub>·Et<sub>2</sub>O–H<sub>2</sub>O Catalytic System.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 7, p. 867, doi. 10.1007/s10593-020-02743-z
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Hypervalent iodine in the structure of N-heterocycles: synthesis, structure, and application in organic synthesis.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 7, p. 854, doi. 10.1007/s10593-020-02742-0
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Synthesis of heterocycles from allenes containing electron-withdrawing substituents under the conditions of electrophilic activation: recent advances.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 7, p. 848, doi. 10.1007/s10593-020-02741-1
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Synthesis of Sulfur-Containing Heterocycles by Electrophilic Addition Reactions of Disulfur Dichloride.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 7, p. 837, doi. 10.1007/s10593-020-02740-2
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Electrophile-Induced Reactions of Cross-Conjugated Enynones in the Synthesis of Heterocycles.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 7, p. 829, doi. 10.1007/s10593-020-02739-9
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Synthesis and reactivity of 1,2,4-oxadiazolium salts.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 7, p. 824, doi. 10.1007/s10593-020-02738-w
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Metal-Free Functionalization of Azine N-Oxides with Electrophilic Reagents.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 7, p. 814, doi. 10.1007/s10593-020-02737-x
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N-Alkylation of Nitrogen Heterocycles with α-Diazocarbonyl Compounds.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 7, p. 809, doi. 10.1007/s10593-020-02736-y
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Synthesis of pyrazoles from α-diazo-β-ketosulfones and α-diazo-β-ketophosphonates.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 7, p. 806, doi. 10.1007/s10593-020-02735-z
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Thematic issue "Synthesis and transformations of heterocycles under electrophilic conditions".
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 7, p. 805, doi. 10.1007/s10593-020-02734-0
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- Article