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Chemical Recycling of Carbon Dioxide to Methanol and Dimethyl Ether: From Greenhouse Gas to Renewable, Environmentally Carbon Neutral Fuels and Synthetic Hydrocarbons
Chemical Recycling of Carbon Dioxide to Methanol and Dimethyl Ether: From Greenhouse Gas to Renewable, Environmentally Carbon Neutral Fuels and Synthetic Hydrocarbons
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Chemical Recycling of Carbon Dioxide to Methanol and Dimethyl Ether: From Greenhouse Gas to Renewable, Environmentally Carbon Neutral Fuels and Synthetic Hydrocarbons

Olah, George A ; Goeppert, Alain ; Prakash, G. K. Surya

Journal of organic chemistry, 2009-01, Vol.74 (2), p.487-498 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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2
Understanding the Reactivity of Captodative Ethylenes in Polar Cycloaddition Reactions. A Theoretical Study
Understanding the Reactivity of Captodative Ethylenes in Polar Cycloaddition Reactions. A Theoretical Study
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Understanding the Reactivity of Captodative Ethylenes in Polar Cycloaddition Reactions. A Theoretical Study

Domingo, Luis R ; Chamorro, Eduardo ; Pérez, Patricia

Journal of organic chemistry, 2008-06, Vol.73 (12), p.4615-4624 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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3
Drying of Organic Solvents: Quantitative Evaluation of the Efficiency of Several Desiccants
Drying of Organic Solvents: Quantitative Evaluation of the Efficiency of Several Desiccants
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Drying of Organic Solvents: Quantitative Evaluation of the Efficiency of Several Desiccants

Williams, D. Bradley G ; Lawton, Michelle

Journal of organic chemistry, 2010-12, Vol.75 (24), p.8351-8354 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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4
Quantum-Chemical Simulation of 1H NMR Spectra. 2. Comparison of DFT-Based Procedures for Computing Proton–Proton Coupling Constants in Organic Molecules
Quantum-Chemical Simulation of 1H NMR Spectra. 2. Comparison of DFT-Based Procedures for Computing Proton–Proton Coupling Constants in Organic Molecules
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Quantum-Chemical Simulation of 1H NMR Spectra. 2. Comparison of DFT-Based Procedures for Computing Proton–Proton Coupling Constants in Organic Molecules

Bally, Thomas ; Rablen, Paul R

Journal of organic chemistry, 2011-06, Vol.76 (12), p.4818-4830 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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5
Equilibrium Acidities of Superacids
Equilibrium Acidities of Superacids
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Equilibrium Acidities of Superacids

Kütt, Agnes ; Rodima, Toomas ; Saame, Jaan ; Raamat, Elin ; Mäemets, Vahur ; Kaljurand, Ivari ; Koppel, Ilmar A ; Garlyauskayte, Romute Yu ; Yagupolskii, Yurii L ; Yagupolskii, Lev M ; Bernhardt, Eduard ; Willner, Helge ; Leito, Ivo

Journal of organic chemistry, 2011-01, Vol.76 (2), p.391-395 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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6
Nonthermal Microwave Effects Revisited:  On the Importance of Internal Temperature Monitoring and Agitation in Microwave Chemistry
Nonthermal Microwave Effects Revisited:  On the Importance of Internal Temperature Monitoring and Agitation in Microwave Chemistry
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Nonthermal Microwave Effects Revisited:  On the Importance of Internal Temperature Monitoring and Agitation in Microwave Chemistry

Herrero, M. Antonia ; Kremsner, Jennifer M ; Kappe, C. Oliver

Journal of organic chemistry, 2008-01, Vol.73 (1), p.36-47 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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7
Organic Triplet Sensitizer Library Derived from a Single Chromophore (BODIPY) with Long-Lived Triplet Excited State for Triplet–Triplet Annihilation Based Upconversion
Organic Triplet Sensitizer Library Derived from a Single Chromophore (BODIPY) with Long-Lived Triplet Excited State for Triplet–Triplet Annihilation Based Upconversion
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Organic Triplet Sensitizer Library Derived from a Single Chromophore (BODIPY) with Long-Lived Triplet Excited State for Triplet–Triplet Annihilation Based Upconversion

Wu, Wanhua ; Guo, Huimin ; Wu, Wenting ; Ji, Shaomin ; Zhao, Jianzhang

Journal of organic chemistry, 2011-09, Vol.76 (17), p.7056-7064 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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8
Cul-Nanoparticles-Catalyzed Selective Synthesis of Phenols, Anilines, and Thiophenols from Aryl Halides in Aqueous Solution
Cul-Nanoparticles-Catalyzed Selective Synthesis of Phenols, Anilines, and Thiophenols from Aryl Halides in Aqueous Solution
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Cul-Nanoparticles-Catalyzed Selective Synthesis of Phenols, Anilines, and Thiophenols from Aryl Halides in Aqueous Solution

XU, Hua-Jian ; LIANG, Yu-Feng ; CAI, Zhen-Ya ; QI, Hong-Xia ; YANG, Chun-Yan ; FENG, Yi-Si

Journal of organic chemistry, 2011-04, Vol.76 (7), p.2296-2300 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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9
Perylene-3,4,9,10-tetracarboxylic Acid Diimides: Synthesis, Physical Properties, and Use in Organic Electronics
Perylene-3,4,9,10-tetracarboxylic Acid Diimides: Synthesis, Physical Properties, and Use in Organic Electronics
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Perylene-3,4,9,10-tetracarboxylic Acid Diimides: Synthesis, Physical Properties, and Use in Organic Electronics

Huang, Chun ; Barlow, Stephen ; Marder, Seth R

Journal of organic chemistry, 2011-04, Vol.76 (8), p.2386-2407 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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10
Low-Valent Iron-Catalyzed C−C Bond Formation−Addition, Substitution, and C−H Bond Activation
Low-Valent Iron-Catalyzed C−C Bond Formation−Addition, Substitution, and C−H Bond Activation
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Low-Valent Iron-Catalyzed C−C Bond Formation−Addition, Substitution, and C−H Bond Activation

Nakamura, Eiichi ; Yoshikai, Naohiko

Journal of organic chemistry, 2010-09, Vol.75 (18), p.6061-6067 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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