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Naoto Chatani

Showing results (1-10 of 173) with videos related to

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Chemical Record (New York, N.Y.)|August 30, 2008
Ruthenium-catalyzed carbonylative cycloaddition reactions involving carbonyl and imino groups as assembling unitsNaoto Chatani
Chemistry, an Asian Journal|August 28, 2025
Catalytic Reactions Involving the Oxidative Addition of Si─Halogen and Si─Pseudohalogen Bonds as a Key StepNaoto Chatani
Accounts of Chemical Research|October 11, 2023
Nickel-Catalyzed Functionalization Reactions Involving C-H Bond Activation via an Amidate-Promoted Strategy and Its Extension to the Activation of C-F, C-O, C-S, and C-CN BondsNaoto Chatani
Chemical Communications (Cambridge, England)|January 4, 2022
Rh(I)-catalysed imine-directed C-H functionalization <i>via</i> the oxidative [3 + 2] cycloaddition of benzylamine derivatives with maleimidesAmrita Das, Naoto Chatani
Journal of the American Chemical Society|February 15, 2021
Transient Imine as a Directing Group for the Metal-Free <i>o</i>-C-H Borylation of BenzaldehydesSupriya Rej, Naoto Chatani
Inorganic Chemistry|March 3, 2021
Effect of Sulfonamide and Carboxamide Ligands on the Structural Diversity of Bimetallic Rh<sup>II</sup>-Rh<sup>II</sup> Cores: Exploring the Catalytic Activity of These Newly Synthesized Rh<sub>2</sub> ComplexesSupriya Rej, Naoto Chatani
Angewandte Chemie (International Ed. in English)|October 10, 2013
Catalytic functionalization of C(sp2)-H and C(sp3)-H bonds by using bidentate directing groupsGuy Rouquet, Naoto Chatani
Topics in Current Chemistry (Cham)|August 31, 2016
Nickel-Catalyzed Cross-Coupling Reactions of Unreactive Phenolic Electrophiles via C-O Bond ActivationMamoru Tobisu, Naoto Chatani
Angewandte Chemie (International Ed. in English)|November 26, 2020
Palladium-Catalyzed Site-Selective [3+2] Annulation via Benzylic and meta C-H Bond ActivationQiyuan He, Naoto Chatani
Organic Letters|September 17, 2014
Rhodium-catalyzed alkylation of C-H bonds in aromatic amides with α,β-unsaturated estersKaname Shibata, Naoto Chatani
Pageof 18

Showing results (1-10 of 173) with videos related to

Sort By:
Pageof 18
Chemical Record (New York, N.Y.)|August 30, 2008
Ruthenium-catalyzed carbonylative cycloaddition reactions involving carbonyl and imino groups as assembling unitsNaoto Chatani
Chemistry, an Asian Journal|August 28, 2025
Catalytic Reactions Involving the Oxidative Addition of Si─Halogen and Si─Pseudohalogen Bonds as a Key StepNaoto Chatani
Accounts of Chemical Research|October 11, 2023
Nickel-Catalyzed Functionalization Reactions Involving C-H Bond Activation via an Amidate-Promoted Strategy and Its Extension to the Activation of C-F, C-O, C-S, and C-CN BondsNaoto Chatani
Chemical Communications (Cambridge, England)|January 4, 2022
Rh(I)-catalysed imine-directed C-H functionalization <i>via</i> the oxidative [3 + 2] cycloaddition of benzylamine derivatives with maleimidesAmrita Das, Naoto Chatani
Journal of the American Chemical Society|February 15, 2021
Transient Imine as a Directing Group for the Metal-Free <i>o</i>-C-H Borylation of BenzaldehydesSupriya Rej, Naoto Chatani
Inorganic Chemistry|March 3, 2021
Effect of Sulfonamide and Carboxamide Ligands on the Structural Diversity of Bimetallic Rh<sup>II</sup>-Rh<sup>II</sup> Cores: Exploring the Catalytic Activity of These Newly Synthesized Rh<sub>2</sub> ComplexesSupriya Rej, Naoto Chatani
Angewandte Chemie (International Ed. in English)|October 10, 2013
Catalytic functionalization of C(sp2)-H and C(sp3)-H bonds by using bidentate directing groupsGuy Rouquet, Naoto Chatani
Topics in Current Chemistry (Cham)|August 31, 2016
Nickel-Catalyzed Cross-Coupling Reactions of Unreactive Phenolic Electrophiles via C-O Bond ActivationMamoru Tobisu, Naoto Chatani
Angewandte Chemie (International Ed. in English)|November 26, 2020
Palladium-Catalyzed Site-Selective [3+2] Annulation via Benzylic and meta C-H Bond ActivationQiyuan He, Naoto Chatani
Organic Letters|September 17, 2014
Rhodium-catalyzed alkylation of C-H bonds in aromatic amides with α,β-unsaturated estersKaname Shibata, Naoto Chatani
Pageof 18