Kinetics and Mechanism of Oxidation of L-proline by Trivalent Copper: A free radical intervention and decarboxylation [PDF]
Mallikarjuna I. Hiremath+2 more
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A silver‐catalyzed decarboxylative coupling of readily available oxamic acids with styrenes to the direct synthesis of E‐cinnamamides has been developed. The reaction pathway was studied and proven to be different from known procedures. Abstract A silver‐catalyzed decarboxylative coupling of oxamic acids with styrenes has been developed to produce E ...
Ru‐Han A+2 more
wiley +1 more source
OXIDATIVE DECARBOXYLATION OF 6-PHOSPHOGLUCONATE IN HETEROLACTIC BACTERIA
Shigetaka Yashima, Kakuo KITAHARA
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The photoinduced decarboxylative radical addition of aryl carboxylic acids, including heteroaromatic carboxylic acids, to electron‐deficient alkenes is achieved in a two‐molecule photoredox system using a combination of biphenyl and 9,10‐dicyanoanthracene without heating or base.
Daisuke Suzuki+5 more
wiley +1 more source
Modular access to alkylfluorides via radical decarboxylative-desulfonylative gem-difunctionalization. [PDF]
Wang X+5 more
europepmc +1 more source
Effects of phenolic compounds on adventitious root formation and oxidative decarboxylation of applied indoleacetic acid in Malus ‘Jork 9’ [PDF]
G.J.M. de Klerk+3 more
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Phase Diagram‐Guided Molten Salt Engineering of Biocarbon Pores at Low Temperatures
This study pioneers a phase diagram‐guided molten salt activation strategy to engineer the pore structure of biocarbon at low temperatures. It achieves a specific surface area of ≈2500 m2 g−1 with tunable pore size at only 500 °C and uncovers the pore evolution mechanism.
Pu Yang+7 more
wiley +1 more source
Heterologous Overexpression of Cytochrome P450BM3 from <i>Bacillus megaterium</i> and Its Role in Gossypol Reduction. [PDF]
Fan W+6 more
europepmc +1 more source
Multifunctional Catalysis Promoted by Solvent Effects: Ti-MCM41 for a One-Pot, Four-Step, Epoxidation–Rearrangement–Oxidation–Decarboxylation Reaction Sequence on Stilbenes and Styrenes [PDF]
José M. Fraile+4 more
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This study develops a series of unimolecular photoinitiators, BP‐S1‐5, by incorporating hydrogen‐donating groups into a benzophenone framework. This method reduces the reliance on co‐initiators, and enables BP‐S1‐5 with efficient photoinitiation and excellent molding capability.
Yu Li+11 more
wiley +1 more source