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The Aerobic Oxidation of p‐Xylene to Terephthalic acid: A Classic Case of Green Chemistry in Action - Partenheimer - - Major Reference Works - Wiley Online Library
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A brief review of para-xylene oxidation to terephthalic acid as a model of primary C–H bond activation - ScienceDirect
![The Aerobic Oxidation of p‐Xylene to Terephthalic acid: A Classic Case of Green Chemistry in Action - Partenheimer - - Major Reference Works - Wiley Online Library The Aerobic Oxidation of p‐Xylene to Terephthalic acid: A Classic Case of Green Chemistry in Action - Partenheimer - - Major Reference Works - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/cb8df510-889e-498f-8fbf-7d7cb19a3a44/nsc004.gif)
The Aerobic Oxidation of p‐Xylene to Terephthalic acid: A Classic Case of Green Chemistry in Action - Partenheimer - - Major Reference Works - Wiley Online Library
![The Aerobic Oxidation of p‐Xylene to Terephthalic acid: A Classic Case of Green Chemistry in Action - Partenheimer - - Major Reference Works - Wiley Online Library The Aerobic Oxidation of p‐Xylene to Terephthalic acid: A Classic Case of Green Chemistry in Action - Partenheimer - - Major Reference Works - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/a2d1df81-e78c-414b-b04c-b7b12c04d0e4/nsc009.gif)
The Aerobic Oxidation of p‐Xylene to Terephthalic acid: A Classic Case of Green Chemistry in Action - Partenheimer - - Major Reference Works - Wiley Online Library
![A brief review of para-xylene oxidation to terephthalic acid as a model of primary C–H bond activation - ScienceDirect A brief review of para-xylene oxidation to terephthalic acid as a model of primary C–H bond activation - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S1872206714601935-fx3.jpg)
A brief review of para-xylene oxidation to terephthalic acid as a model of primary C–H bond activation - ScienceDirect
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Process for the industrial oxidation of p-xylene to terephthalic acid. | Download Scientific Diagram
![The Aerobic Oxidation of p‐Xylene to Terephthalic acid: A Classic Case of Green Chemistry in Action - Partenheimer - - Major Reference Works - Wiley Online Library The Aerobic Oxidation of p‐Xylene to Terephthalic acid: A Classic Case of Green Chemistry in Action - Partenheimer - - Major Reference Works - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/bdbb2e11-eead-452a-b7f4-11f9e4ef63d4/nsc005.gif)
The Aerobic Oxidation of p‐Xylene to Terephthalic acid: A Classic Case of Green Chemistry in Action - Partenheimer - - Major Reference Works - Wiley Online Library
![SciELO - Brasil - Analysis of impurities in crude and highly-purified terephthalic acid by capillary electrophoresis Analysis of impurities in crude and highly-purified terephthalic acid by capillary electrophoresis SciELO - Brasil - Analysis of impurities in crude and highly-purified terephthalic acid by capillary electrophoresis Analysis of impurities in crude and highly-purified terephthalic acid by capillary electrophoresis](https://minio.scielo.br/documentstore/1678-4790/jBz3d7BVq7qV6hsv9ZpZ8km/0805a5b27f4c815531bc78379c157bd4c6ab3953.gif)
SciELO - Brasil - Analysis of impurities in crude and highly-purified terephthalic acid by capillary electrophoresis Analysis of impurities in crude and highly-purified terephthalic acid by capillary electrophoresis
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Catalysts | Free Full-Text | Manganese and Cobalt Doped Hierarchical Mesoporous Halloysite-Based Catalysts for Selective Oxidation of p-Xylene to Terephthalic Acid | HTML
The sustainable room temperature conversion of p-xylene to terephthalic acid using ozone and UV irradiation - Green Chemistry (RSC Publishing)
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A brief review of para-xylene oxidation to terephthalic acid as a model of primary C–H bond activation - ScienceDirect
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A brief review of para-xylene oxidation to terephthalic acid as a model of primary C–H bond activation - ScienceDirect
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Synthesis of terephthalic acid via Diels-Alder reactions with ethylene and oxidized variants of 5-hydroxymethylfurfural | PNAS
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Biotransformation of p-xylene into terephthalic acid by engineered Escherichia coli | Nature Communications
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