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Refinado por: Nome da Publicação: Journal Of Organic Chemistry remover assunto: Stereoisomerism remover
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CuO Nanoparticles Catalyzed C−N, C−O, and C−S Cross-Coupling Reactions: Scope and Mechanism
CuO Nanoparticles Catalyzed C−N, C−O, and C−S Cross-Coupling Reactions: Scope and Mechanism
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CuO Nanoparticles Catalyzed C−N, C−O, and C−S Cross-Coupling Reactions: Scope and Mechanism

Jammi, Suribabu ; Sakthivel, Sekarpandi ; Rout, Laxmidhar ; Mukherjee, Tathagata ; Mandal, Santu ; Mitra, Raja ; Saha, Prasenjit ; Punniyamurthy, Tharmalingam

Journal of organic chemistry, 2009-03, Vol.74 (5), p.1971-1976 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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2
Palladium-Catalyzed Carbonylation Reactions of Aryl Bromides at Atmospheric Pressure: A General System Based on Xantphos
Palladium-Catalyzed Carbonylation Reactions of Aryl Bromides at Atmospheric Pressure: A General System Based on Xantphos
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Palladium-Catalyzed Carbonylation Reactions of Aryl Bromides at Atmospheric Pressure: A General System Based on Xantphos

Martinelli, Joseph R ; Watson, Donald A ; Freckmann, Dominique M. M ; Barder, Timothy E ; Buchwald, Stephen L

Journal of organic chemistry, 2008-09, Vol.73 (18), p.7102-7107 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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3
Lewis Acid Promoted Diastereoselective Addition of TMSCN and TMSCF3 to Isatin-Derived N‑Sulfinyl Ketimines: Synthesis of Optically Active Tetrasubstituted 3‑Aminooxindoles
Lewis Acid Promoted Diastereoselective Addition of TMSCN and TMSCF3 to Isatin-Derived N‑Sulfinyl Ketimines: Synthesis of Optically Active Tetrasubstituted 3‑Aminooxindoles
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Lewis Acid Promoted Diastereoselective Addition of TMSCN and TMSCF3 to Isatin-Derived N‑Sulfinyl Ketimines: Synthesis of Optically Active Tetrasubstituted 3‑Aminooxindoles

Chen, Diao ; Xu, Ming-Hua

Journal of organic chemistry, 2014-08, Vol.79 (16), p.7746-7751 [Periódico revisado por pares]

United States: American Chemical Society

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4
Preparation of 3,5-Disubstituted Pyrazoles and Isoxazoles from Terminal Alkynes, Aldehydes, Hydrazines, and Hydroxylamine
Preparation of 3,5-Disubstituted Pyrazoles and Isoxazoles from Terminal Alkynes, Aldehydes, Hydrazines, and Hydroxylamine
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Preparation of 3,5-Disubstituted Pyrazoles and Isoxazoles from Terminal Alkynes, Aldehydes, Hydrazines, and Hydroxylamine

Harigae, Ryo ; Moriyama, Katsuhiko ; Togo, Hideo

Journal of organic chemistry, 2014-03, Vol.79 (5), p.2049-2058 [Periódico revisado por pares]

United States: American Chemical Society

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5
Organocatalytic Enantioselective Pictet–Spengler Reactions for the Syntheses of 1‑Substituted 1,2,3,4-Tetrahydroisoquinolines
Organocatalytic Enantioselective Pictet–Spengler Reactions for the Syntheses of 1‑Substituted 1,2,3,4-Tetrahydroisoquinolines
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Organocatalytic Enantioselective Pictet–Spengler Reactions for the Syntheses of 1‑Substituted 1,2,3,4-Tetrahydroisoquinolines

Mons, Elma ; Wanner, Martin J ; Ingemann, Steen ; van Maarseveen, Jan H ; Hiemstra, Henk

Journal of organic chemistry, 2014-08, Vol.79 (16), p.7380-7390 [Periódico revisado por pares]

United States: American Chemical Society

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6
Epi-Cinchona Based Thiourea Organocatalyst Family as an Efficient Asymmetric Michael Addition Promoter: Enantioselective Conjugate Addition of Nitroalkanes to Chalcones and α,β-Unsaturated N-Acylpyrroles
Epi-Cinchona Based Thiourea Organocatalyst Family as an Efficient Asymmetric Michael Addition Promoter: Enantioselective Conjugate Addition of Nitroalkanes to Chalcones and α,β-Unsaturated N-Acylpyrroles
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Epi-Cinchona Based Thiourea Organocatalyst Family as an Efficient Asymmetric Michael Addition Promoter: Enantioselective Conjugate Addition of Nitroalkanes to Chalcones and α,β-Unsaturated N-Acylpyrroles

Vakulya, Benedek ; Varga, Szilárd ; Soós, Tibor

Journal of organic chemistry, 2008-05, Vol.73 (9), p.3475-3480 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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7
Enhanced anti-Diastereo- and Enantioselectivity in Alcohol-Mediated Carbonyl Crotylation Using an Isolable Single Component Iridium Catalyst
Enhanced anti-Diastereo- and Enantioselectivity in Alcohol-Mediated Carbonyl Crotylation Using an Isolable Single Component Iridium Catalyst
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Enhanced anti-Diastereo- and Enantioselectivity in Alcohol-Mediated Carbonyl Crotylation Using an Isolable Single Component Iridium Catalyst

Gao, Xin ; Townsend, Ian A ; Krische, Michael J

Journal of organic chemistry, 2011-04, Vol.76 (7), p.2350-2354 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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8
Casuarine Stereoisomers from Achiral Substrates: Chemoenzymatic Synthesis and Inhibitory Properties
Casuarine Stereoisomers from Achiral Substrates: Chemoenzymatic Synthesis and Inhibitory Properties
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Casuarine Stereoisomers from Achiral Substrates: Chemoenzymatic Synthesis and Inhibitory Properties

Concia, Alda Lisa ; Gómez, Livia ; Parella, Teodor ; Joglar, Jesús ; Clapés, Pere

Journal of organic chemistry, 2014-06, Vol.79 (11), p.5386-5389 [Periódico revisado por pares]

United States: American Chemical Society

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9
Iron Halide-Mediated Regio- and Stereoselective Halosulfonylation of Terminal Alkynes with Sulfonylhydrazides: Synthesis of (E)‑β-Chloro and Bromo Vinylsulfones
Iron Halide-Mediated Regio- and Stereoselective Halosulfonylation of Terminal Alkynes with Sulfonylhydrazides: Synthesis of (E)‑β-Chloro and Bromo Vinylsulfones
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Iron Halide-Mediated Regio- and Stereoselective Halosulfonylation of Terminal Alkynes with Sulfonylhydrazides: Synthesis of (E)‑β-Chloro and Bromo Vinylsulfones

Li, Xiaoqing ; Shi, Xinhua ; Fang, Mingwu ; Xu, Xiangsheng

Journal of organic chemistry, 2013-09, Vol.78 (18), p.9499-9504 [Periódico revisado por pares]

United States: American Chemical Society

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10
Metal Triflate-Catalyzed Cationic Benzylation and Allylation of 1,3-Dicarbonyl Compounds
Metal Triflate-Catalyzed Cationic Benzylation and Allylation of 1,3-Dicarbonyl Compounds
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Metal Triflate-Catalyzed Cationic Benzylation and Allylation of 1,3-Dicarbonyl Compounds

Noji, Masahiro ; Konno, Yosuke ; Ishii, Keitaro

Journal of organic chemistry, 2007-07, Vol.72 (14), p.5161-5167 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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