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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
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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3
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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4
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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5
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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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
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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9
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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10
Rhodium Carbene Routes to Oxazoles and Thiazoles. Catalyst Effects in the Synthesis of Oxazole and Thiazole Carboxylates, Phosphonates, and Sulfones
Rhodium Carbene Routes to Oxazoles and Thiazoles. Catalyst Effects in the Synthesis of Oxazole and Thiazole Carboxylates, Phosphonates, and Sulfones
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Rhodium Carbene Routes to Oxazoles and Thiazoles. Catalyst Effects in the Synthesis of Oxazole and Thiazole Carboxylates, Phosphonates, and Sulfones

Shi, Baolu ; Blake, Alexander J ; Lewis, William ; Campbell, Ian B ; Judkins, Brian D ; Moody, Christopher J

Journal of organic chemistry, 2010-01, Vol.75 (1), p.152-161 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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