This work deals with the coupling of model bioactive carboxylic acids (l-naphthylacetic acid, 2-(6-methoxy-2-naphthyl)propionic acid (naproxen) and nicotinic acid) to dextran by direct reaction with their potassium salts using pyridine/sulfonyl chloride as activating agent. The structure of the resu
Controlled, regiospecific oxidation of pyridine carboxylic acids and esters with elemental fluorine
✍ Scribed by Michael Van Der Puy; David Nalewajek; Gene E. Wicks
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- French
- Weight
- 206 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Pyridine carboxylic acid salts or esters in water or wateracetonitrile mixtures were treated with elemental fluorine to give the corresponding 2-pyridones. Elemental fluorine is a potent oxidizer, but aside from fluorinations, has seldom been used for the controlled oxidation of organic substances. I,2 Recently, Rosen3 has described the use of acetyl hypofluorite as a reagent to
📜 SIMILAR VOLUMES
## Abstract Summary: In non‐polar solvents such as toluene, Cp‐Ni and ‐Pd complexes (Cp = __η__^5^‐C~5~H~5~) with appropriate activators have been found to induce the addition polymerization of norbornene in excellent yields, for example (Cp)Pd(allyl)/[Ph~3~C][B(C~6~F~5~)~4~] gave 105 120 kg‐polyme