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Refinado por: Nome da Publicação: The Journal Of Organic Chemistry remover idioma: Japonês remover
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Synthesis of Azaheterocycles from Aryl Ketone O-Acetyl Oximes and Internal Alkynes by Cu–Rh Bimetallic Relay Catalysts
Synthesis of Azaheterocycles from Aryl Ketone O-Acetyl Oximes and Internal Alkynes by Cu–Rh Bimetallic Relay Catalysts
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Synthesis of Azaheterocycles from Aryl Ketone O-Acetyl Oximes and Internal Alkynes by Cu–Rh Bimetallic Relay Catalysts

Too, Pei Chui ; Chua, Sze Hui ; Wong, Siong Heng ; Chiba, Shunsuke

Journal of organic chemistry, 2011-08, Vol.76 (15), p.6159-6168 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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2
Constructing Quaternary Carbons from N‑(Acyloxy)phthalimide Precursors of Tertiary Radicals Using Visible-Light Photocatalysis
Constructing Quaternary Carbons from N‑(Acyloxy)phthalimide Precursors of Tertiary Radicals Using Visible-Light Photocatalysis
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Constructing Quaternary Carbons from N‑(Acyloxy)phthalimide Precursors of Tertiary Radicals Using Visible-Light Photocatalysis

Pratsch, Gerald ; Lackner, Gregory L ; Overman, Larry E

Journal of organic chemistry, 2015-06, Vol.80 (12), p.6025-6036 [Periódico revisado por pares]

United States: American Chemical Society

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3
Construction of Nitrogen Heterocycles Bearing an Aminomethyl Group by Copper-Catalyzed Domino Three-Component Coupling−Cyclization
Construction of Nitrogen Heterocycles Bearing an Aminomethyl Group by Copper-Catalyzed Domino Three-Component Coupling−Cyclization
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Construction of Nitrogen Heterocycles Bearing an Aminomethyl Group by Copper-Catalyzed Domino Three-Component Coupling−Cyclization

Ohta, Yusuke ; Chiba, Hiroaki ; Oishi, Shinya ; Fujii, Nobutaka ; Ohno, Hiroaki

Journal of organic chemistry, 2009-09, Vol.74 (18), p.7052-7058 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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4
Three-Component Coupling of Aldehydes, Aminopyrazoles, and Sulfoxonium Ylides via Rhodium(III)-Catalyzed Imidoyl C–H Activation: Synthesis of Pyrazolo[1,5‑a]pyrimidines
Three-Component Coupling of Aldehydes, Aminopyrazoles, and Sulfoxonium Ylides via Rhodium(III)-Catalyzed Imidoyl C–H Activation: Synthesis of Pyrazolo[1,5‑a]pyrimidines
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Three-Component Coupling of Aldehydes, Aminopyrazoles, and Sulfoxonium Ylides via Rhodium(III)-Catalyzed Imidoyl C–H Activation: Synthesis of Pyrazolo[1,5‑a]pyrimidines

Hoang, Gia L ; Streit, Andrew D ; Ellman, Jonathan A

Journal of organic chemistry, 2018-12, Vol.83 (24), p.15347-15360 [Periódico revisado por pares]

United States: American Chemical Society

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5
The Palladium-Catalyzed Intermolecular C–H Chalcogenation of Arenes
The Palladium-Catalyzed Intermolecular C–H Chalcogenation of Arenes
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The Palladium-Catalyzed Intermolecular C–H Chalcogenation of Arenes

Qiu, Renhua ; Reddy, Vutukuri Prakash ; Iwasaki, Takanori ; Kambe, Nobuaki

Journal of organic chemistry, 2015-01, Vol.80 (1), p.367-374 [Periódico revisado por pares]

United States: American Chemical Society

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6
TPGS-750-M: A Second-Generation Amphiphile for Metal-Catalyzed Cross-Couplings in Water at Room Temperature
TPGS-750-M: A Second-Generation Amphiphile for Metal-Catalyzed Cross-Couplings in Water at Room Temperature
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TPGS-750-M: A Second-Generation Amphiphile for Metal-Catalyzed Cross-Couplings in Water at Room Temperature

Lipshutz, Bruce H ; Ghorai, Subir ; Abela, Alexander R ; Moser, Ralph ; Nishikata, Takashi ; Duplais, Christophe ; Krasovskiy, Arkady ; Gaston, Ricky D ; Gadwood, Robert C

Journal of organic chemistry, 2011-06, Vol.76 (11), p.4379-4391 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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7
Mechanistic Studies on the Cu-Catalyzed Three-Component Reactions of Sulfonyl Azides, 1-Alkynes and Amines, Alcohols, or Water: Dichotomy via a Common Pathway
Mechanistic Studies on the Cu-Catalyzed Three-Component Reactions of Sulfonyl Azides, 1-Alkynes and Amines, Alcohols, or Water: Dichotomy via a Common Pathway
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Mechanistic Studies on the Cu-Catalyzed Three-Component Reactions of Sulfonyl Azides, 1-Alkynes and Amines, Alcohols, or Water: Dichotomy via a Common Pathway

Yoo, Eun Jeong ; Ahlquist, Mårten ; Bae, Imhyuck ; Sharpless, K. Barry ; Fokin, Valery V ; Chang, Sukbok

Journal of organic chemistry, 2008-07, Vol.73 (14), p.5520-5528 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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8
Impregnated Ruthenium on Magnetite as a Recyclable Catalyst for the N-Alkylation of Amines, Sulfonamides, Sulfinamides, and Nitroarenes Using Alcohols as Electrophiles by a Hydrogen Autotransfer Process
Impregnated Ruthenium on Magnetite as a Recyclable Catalyst for the N-Alkylation of Amines, Sulfonamides, Sulfinamides, and Nitroarenes Using Alcohols as Electrophiles by a Hydrogen Autotransfer Process
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Impregnated Ruthenium on Magnetite as a Recyclable Catalyst for the N-Alkylation of Amines, Sulfonamides, Sulfinamides, and Nitroarenes Using Alcohols as Electrophiles by a Hydrogen Autotransfer Process

Cano, Rafael ; Ramón, Diego J ; Yus, Miguel

Journal of organic chemistry, 2011-07, Vol.76 (14), p.5547-5557 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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9
Exploring Catalyst and Solvent Effects in the Multicomponent Synthesis of Pyridine-3,5-dicarbonitriles
Exploring Catalyst and Solvent Effects in the Multicomponent Synthesis of Pyridine-3,5-dicarbonitriles
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Exploring Catalyst and Solvent Effects in the Multicomponent Synthesis of Pyridine-3,5-dicarbonitriles

Guo, Kai ; Thompson, Mark J ; Chen, Beining

Journal of organic chemistry, 2009-09, Vol.74 (18), p.6999-7006 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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10
“Nok”: A Phytosterol-Based Amphiphile Enabling Transition-Metal-Catalyzed Couplings in Water at Room Temperature
“Nok”: A Phytosterol-Based Amphiphile Enabling Transition-Metal-Catalyzed Couplings in Water at Room Temperature
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“Nok”: A Phytosterol-Based Amphiphile Enabling Transition-Metal-Catalyzed Couplings in Water at Room Temperature

Klumphu, Piyatida ; Lipshutz, Bruce H

Journal of organic chemistry, 2014-02, Vol.79 (3), p.888-900 [Periódico revisado por pares]

United States: American Chemical Society

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