Results 181 to 190 of about 88,910 (336)

Identification of Urethanases for Biocatalytic Recycling of Toluene Diisocyanate‐ and Methylene Diphenyl Diisocyanate‐Based Polyurethanes

open access: yesChemSusChem, EarlyView.
Sequence similarity analysis led to the identification of novel urethanases capable of hydrolyzing industrially significant carbamates derived from chemical recycling, such as methanolysis. This allows a combined chemical and enzymatic recycling strategy, which facilitates the depolymerization of polyether‐polyurethane into dicarbamates and ultimately ...
Linda Pastor   +7 more
wiley   +1 more source

Detection of Organophosphorus, Pyrethroid, and Carbamate Pesticides in Tomato Peels: A Spectroscopic Study. [PDF]

open access: yesFoods
López-Benítez A   +5 more
europepmc   +1 more source

Novel Asymmetric Iron Porphyrins for Photocatalytic CO2 Reduction to CH4

open access: yesChemSusChem, EarlyView.
Two novel asymmetric porphyrin‐based iron complexes capable of performing photocatalytic CO2 reduction (CO2R) to CO and CH4 with an organic photosensitizer are presented. 13CO2 labeling studies confirm CH4 is formed by CO2R. These earth‐abundant based complexes show significant potential for efficient CO2R beyond two electrons, joining a single ...
Edelman José Espinoza‐Suárez   +5 more
wiley   +1 more source

Hydrogen peroxide ‐ responsive aminoferrocene prodrugs

open access: yesEuropean Journal of Organic Chemistry, Accepted Article.
Aminoferrocene (AF)‐based prodrugs are activated in cancer cells through reactions with H₂O₂ and other reactive oxygen species (ROS), generating electron‐rich AF’s. These, in turn, induce the production of highly toxic O2·‐ and HO·, leading to cancer cell death.
Marlies Körber   +3 more
wiley   +1 more source

Structure-Activity Relationship Studies of Emtricitabine Prodrugs toward Long-Acting Antiretroviral Formulations. [PDF]

open access: yesACS Omega
Al-Khouja A   +7 more
europepmc   +1 more source

Cross‐Coupling Reactions in Aqueous Micellar Media

open access: yesEuropean Journal of Organic Chemistry, Accepted Article.
Thanks to their ability to efficiently and reliably construct carbon‐carbon and carbon‐heteroatom bonds, cross‐coupling reactions remain at the forefront of chemical research in both academic and industrial settings. However, the growing emphasis on sustainability has exposed the shortcomings of cross‐coupling chemistry in several areas, including the ...
Alexander Uner, Liam Thomas Ball
wiley   +1 more source

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