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- W1655664564 endingPage "79" @default.
- W1655664564 startingPage "37" @default.
- W1655664564 abstract "Publisher Summary The pyrrole ring is widely distributed in nature. It occurs in both terrestrial and marine plants and animals. Examples of simple pyrroles include the Pseudomonas metabolite pyrrolnitrin, a recently discovered seabird hexahalogenated bipyrrole, and an ant trail pheromone. An illustration of the abundant complex natural pyrroles is konbu’acidin A, a sponge metabolite that inhibits cyclin dependent kinase 4. The enormous reactivity of pyrrole in electrophilic substitution reactions explains the occurrence of more than 100 naturally occurring halogenated pyrroles. Following the discovery of the unique electronic properties of polypyrrole, numerous polymers of pyrrole have been crafted. A copolymer of pyrrole and pyrrole-3-carboxylic acid is used in a glucose biosensor, and a copolymer of pyrrole and N -methylpyrrole operates as a redox-switching device. Self-doping, low-band gap, and photorefractive pyrrole polymers have been synthesized, and some examples are illustrated in the chapter. The pyrrole ring has found great use in the design and development of pharmaceuticals. Lipitor is the leading cholesterol lowing drug and other bioactive pyrroles include the opioid antagonist norbinaltorphimine, a broad-spectrum insecticide, a sodium-independent dopamine receptor antagonist, a DNA cross-linking agent, and an antipsychotic agent." @default.
- W1655664564 created "2016-06-24" @default.
- W1655664564 creator A5049245360 @default.
- W1655664564 date "2007-01-01" @default.
- W1655664564 modified "2023-10-09" @default.
- W1655664564 title "Chapter 2 Pyrroles" @default.
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