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Refinado por: Nome da Publicação: Journal Of Organic Chemistry remover idioma: Japonês remover
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1
Transition-Metal-Free and Visible-Light-Mediated Desulfonylation and Dehalogenation Reactions: Hantzsch Ester Anion as Electron and Hydrogen Atom Donor
Transition-Metal-Free and Visible-Light-Mediated Desulfonylation and Dehalogenation Reactions: Hantzsch Ester Anion as Electron and Hydrogen Atom Donor
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Transition-Metal-Free and Visible-Light-Mediated Desulfonylation and Dehalogenation Reactions: Hantzsch Ester Anion as Electron and Hydrogen Atom Donor

Heredia, Micaela D ; Guerra, Walter D ; Barolo, Silvia M ; Fornasier, Santiago J ; Rossi, Roberto A ; Budén, María E

Journal of organic chemistry, 2020-11, Vol.85 (21), p.13481-13494 [Periódico revisado por pares]

American Chemical Society

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2
Initiation in Photoredox C–H Functionalization Reactions. Is Dimsyl Anion a Key Ingredient?
Initiation in Photoredox C–H Functionalization Reactions. Is Dimsyl Anion a Key Ingredient?
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Initiation in Photoredox C–H Functionalization Reactions. Is Dimsyl Anion a Key Ingredient?

Budén, María E ; Bardagí, Javier I ; Puiatti, Marcelo ; Rossi, Roberto A

Journal of organic chemistry, 2017-08, Vol.82 (16), p.8325-8333 [Periódico revisado por pares]

United States: American Chemical Society

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3
“Transition-Metal-Free” Synthesis of Carbazoles by Photostimulated Reactions of 2′-Halo[1,1′-biphenyl]-2-amines
“Transition-Metal-Free” Synthesis of Carbazoles by Photostimulated Reactions of 2′-Halo[1,1′-biphenyl]-2-amines
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“Transition-Metal-Free” Synthesis of Carbazoles by Photostimulated Reactions of 2′-Halo[1,1′-biphenyl]-2-amines

Guerra, Walter D ; Rossi, Roberto A ; Pierini, Adriana B ; Barolo, Silvia M

Journal of organic chemistry, 2015-01, Vol.80 (2), p.928-941 [Periódico revisado por pares]

United States: American Chemical Society

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4
Room-Temperature and Transition-Metal-Free Mizoroki–Heck-type Reaction. Synthesis of E‑Stilbenes by Photoinduced C–H Functionalization
Room-Temperature and Transition-Metal-Free Mizoroki–Heck-type Reaction. Synthesis of E‑Stilbenes by Photoinduced C–H Functionalization
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Room-Temperature and Transition-Metal-Free Mizoroki–Heck-type Reaction. Synthesis of E‑Stilbenes by Photoinduced C–H Functionalization

Guastavino, Javier F ; Budén, María E ; Rossi, Roberto A

Journal of organic chemistry, 2014-10, Vol.79 (19), p.9104-9111 [Periódico revisado por pares]

United States: American Chemical Society

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5
Synthesis of Carbazoles by Intramolecular Arylation of Diarylamide Anions
Synthesis of Carbazoles by Intramolecular Arylation of Diarylamide Anions
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Synthesis of Carbazoles by Intramolecular Arylation of Diarylamide Anions

Budén, María E ; Vaillard, Victoria A ; Martin, Sandra E ; Rossi, Roberto A

Journal of organic chemistry, 2009-06, Vol.74 (12), p.4490-4498 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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6
Electron-Transfer-Mediated Synthesis of Phenanthridines by Intramolecular Arylation of Anions from N-(ortho-Halobenzyl)arylamines: Regiochemical and Mechanistic Analysis
Electron-Transfer-Mediated Synthesis of Phenanthridines by Intramolecular Arylation of Anions from N-(ortho-Halobenzyl)arylamines: Regiochemical and Mechanistic Analysis
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Electron-Transfer-Mediated Synthesis of Phenanthridines by Intramolecular Arylation of Anions from N-(ortho-Halobenzyl)arylamines: Regiochemical and Mechanistic Analysis

Budén, María E ; Dorn, Viviana B ; Gamba, Martina ; Pierini, Adriana B ; Rossi, Roberto A

Journal of organic chemistry, 2010-04, Vol.75 (7), p.2206-2218 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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7
Short Access to 6-Substituted Pyrimidine Derivatives by the SRN1 Mechanism. Synthesis of 6-Substituted Uracils through a One-Pot Procedure
Short Access to 6-Substituted Pyrimidine Derivatives by the SRN1 Mechanism. Synthesis of 6-Substituted Uracils through a One-Pot Procedure
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Short Access to 6-Substituted Pyrimidine Derivatives by the SRN1 Mechanism. Synthesis of 6-Substituted Uracils through a One-Pot Procedure

Bardagí, Javier I ; Rossi, Roberto A

Journal of organic chemistry, 2010-08, Vol.75 (15), p.5271-5277 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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8
Triorganostannylation of Halo- and Dihaloadamantanes and 5-Chloro-2-adamantanone in Liquid Ammonia by the SRN1 Mechanism. Relative Reactivity of Nucleophiles and Bridgehead Halides
Triorganostannylation of Halo- and Dihaloadamantanes and 5-Chloro-2-adamantanone in Liquid Ammonia by the SRN1 Mechanism. Relative Reactivity of Nucleophiles and Bridgehead Halides
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Triorganostannylation of Halo- and Dihaloadamantanes and 5-Chloro-2-adamantanone in Liquid Ammonia by the SRN1 Mechanism. Relative Reactivity of Nucleophiles and Bridgehead Halides

Santiago, Ana N ; Toledo, Carlos A ; Rossi, Roberto A

Journal of organic chemistry, 2002-04, Vol.67 (8), p.2494-2500 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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9
Intramolecular Electron Transfer Reactions Catalyzed by .alpha.-Oxo and .beta.-Oxo Substituents in the 1-Chlorobicyclo[2.2.1]heptane System
Intramolecular Electron Transfer Reactions Catalyzed by .alpha.-Oxo and .beta.-Oxo Substituents in the 1-Chlorobicyclo[2.2.1]heptane System
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Intramolecular Electron Transfer Reactions Catalyzed by .alpha.-Oxo and .beta.-Oxo Substituents in the 1-Chlorobicyclo[2.2.1]heptane System

Lukach, Andres E ; Morris, David G ; Santiago, Ana N ; Rossi, Roberto A

Journal of organic chemistry, 1995-02, Vol.60 (4), p.1000-1004 [Periódico revisado por pares]

American Chemical Society

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10
The reactivity of 1-chloro-3,3-dimethylbicyclo[2.2.2]octan-2-one in the radical mechanism of nucleophilic substitution
The reactivity of 1-chloro-3,3-dimethylbicyclo[2.2.2]octan-2-one in the radical mechanism of nucleophilic substitution
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The reactivity of 1-chloro-3,3-dimethylbicyclo[2.2.2]octan-2-one in the radical mechanism of nucleophilic substitution

Santiago, Ana N ; Takeuchi, Ken'ichi ; Ohga, Yasushi ; Nishida, Mitsuo ; Rossi, Roberto A

Journal of organic chemistry, 1991-02, Vol.56 (4), p.1581-1584 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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