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Alkyne Elementometalation−Pd-Catalyzed Cross-Coupling. Toward Synthesis of All Conceivable Types of Acyclic Alkenes in High Yields, Efficiently, Selectively, Economically, and Safely: “Green” Way
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Alkyne Elementometalation−Pd-Catalyzed Cross-Coupling. Toward Synthesis of All Conceivable Types of Acyclic Alkenes in High Yields, Efficiently, Selectively, Economically, and Safely: “Green” Way

Negishi, Ei-ichi ; Wang, Guangwei ; Rao, Honghua ; Xu, Zhaoqing

Journal of organic chemistry, 2010-05, Vol.75 (10), p.3151-3182 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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2
Establishment of Broadly Applicable Reaction Conditions for the Palladium-Catalyzed Direct Arylation of Heteroatom-Containing Aromatic Compounds
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Establishment of Broadly Applicable Reaction Conditions for the Palladium-Catalyzed Direct Arylation of Heteroatom-Containing Aromatic Compounds

Liégault, Benoît ; Lapointe, David ; Caron, Laurence ; Vlassova, Anna ; Fagnou, Keith

Journal of organic chemistry, 2009-03, Vol.74 (5), p.1826-1834 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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3
Organoiodine(V) Reagents in Organic Synthesis
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Organoiodine(V) Reagents in Organic Synthesis

Zhdankin, Viktor V

Journal of organic chemistry, 2011-03, Vol.76 (5), p.1185-1197 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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4
Room Temperature Aryl Trifluoromethylation via Copper-Mediated Oxidative Cross-Coupling
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Room Temperature Aryl Trifluoromethylation via Copper-Mediated Oxidative Cross-Coupling

Senecal, Todd D ; Parsons, Andrew T ; Buchwald, Stephen L

Journal of organic chemistry, 2011-02, Vol.76 (4), p.1174-1176 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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5
Imidazo[1,2-a]pyridines Susceptible to Excited State Intramolecular Proton Transfer: One-Pot Synthesis via an Ortoleva–King Reaction
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Imidazo[1,2-a]pyridines Susceptible to Excited State Intramolecular Proton Transfer: One-Pot Synthesis via an Ortoleva–King Reaction

Stasyuk, Anton J ; Banasiewicz, Marzena ; Cyrański, Michał K ; Gryko, Daniel T

Journal of organic chemistry, 2012-07, Vol.77 (13), p.5552-5558 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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6
Aiming for the Ideal Synthesis
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Aiming for the Ideal Synthesis

Gaich, Tanja ; Baran, Phil S

Journal of organic chemistry, 2010-07, Vol.75 (14), p.4657-4673 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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7
Selective Syntheses of [7]–[12]Cycloparaphenylenes Using Orthogonal Suzuki–Miyaura Cross-Coupling Reactions
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Selective Syntheses of [7]–[12]Cycloparaphenylenes Using Orthogonal Suzuki–Miyaura Cross-Coupling Reactions

Darzi, Evan R ; Sisto, Thomas J ; Jasti, Ramesh

Journal of organic chemistry, 2012-08, Vol.77 (15), p.6624-6628 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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8
Copper-Catalyzed Thiolation of the Di- or Trimethoxybenzene Arene C−H Bond with Disulfides
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Copper-Catalyzed Thiolation of the Di- or Trimethoxybenzene Arene C−H Bond with Disulfides

Zhang, Shouhui ; Qian, Pengcheng ; Zhang, Manli ; Hu, Maolin ; Cheng, Jiang

Journal of organic chemistry, 2010-10, Vol.75 (19), p.6732-6735 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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9
BINOL-Based Fluorescent Sensor for Recognition of Cu(II) and Sulfide Anion in Water
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BINOL-Based Fluorescent Sensor for Recognition of Cu(II) and Sulfide Anion in Water

Wang, Ming-Qi ; Li, Kun ; Hou, Ji-Ting ; Wu, Ming-Yu ; Huang, Zeng ; Yu, Xiao-Qi

Journal of organic chemistry, 2012-09, Vol.77 (18), p.8350-8354 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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10
Geometry Relaxation-Induced Large Stokes Shift in Red-Emitting Borondipyrromethenes (BODIPY) and Applications in Fluorescent Thiol Probes
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Geometry Relaxation-Induced Large Stokes Shift in Red-Emitting Borondipyrromethenes (BODIPY) and Applications in Fluorescent Thiol Probes

Chen, Yinghui ; Zhao, Jianzhang ; Guo, Huimin ; Xie, Lijuan

Journal of organic chemistry, 2012-03, Vol.77 (5), p.2192-2206 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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