Transition Metal-Catalyzed Direct C(sp<sup>3</sup>)-H Functionalization Reactions of Aliphatic Carboxylic Acids. [PDF]
Mal S, van Gemmeren M.
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Formal Diels-Alder reaction of saturated carboxylic acids via C-H activation. [PDF]
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Transhepatic Gradients Reveal Selective Hepatic Processing Defects With Systemic Consequences in Cirrhosis. [PDF]
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Antimicrobial Activity of Metal-Based Danofloxacin Complexes Against Pathogenic Microorganisms. [PDF]
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From Mono-<i>N</i>-Protected Amino Acids to Pyridones: A Decade of Evolution of Bifunctional Ligands for Pd(II)-Catalyzed C-H Activation. [PDF]
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Dietary resveratrol improves meat quality and antioxidant capacity of Tibetan sheep by regulating muscle fiber characteristics and mitochondrial function. [PDF]
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Identification of potential NAD-related biomarkers of recurrent miscarriage risk. [PDF]
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2,3-Dihydro-4-pyridone skeleton is an important building block in organic synthesis because it features several reaction sites with nucleophilic or electrophilic properties. Herein, we disclose a method for its formation by intramolecular cyclization of ester-tethered enaminones, which can easily be synthesized from readily available materials, such as
Milovan Stojanović +2 more
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The novel and effective diastereoselective synthesis of multifunctionalized dihydropyridones, including CF3-substituted derivatives, has been developed on the basis of the piperidine-promoted domino reaction of carbamoylated enaminones with aldehydes.
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Synthesis of Some N-dialkylaminoalkyl-4-pyridones
Journal of the American Pharmaceutical Association (Scientific ed.), 1950Attempts to prepare some N-dialkylaminoalkyl-4-alkoxy- and 4-aryloxy-2-pyridones by oxidation of N-dialkylaminoalkyl-4-alkoxy- and 4-aryloxy-pyridinium halides with potassium ferricyanide in alkaline solution resulted instead in the formation of N-dialkylaminoalkyl-4-pyridones as a result of cleavage of the 4-alkoxy or 4-aryloxy group under the ...
J H, SHINKAI, L M, PARKS
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