C-phosphorylation of 2,5-dimethyl-N-arylpyrroles
β Scribed by Andrei A. Tolmachev; Sergei P. Ivonin; Alksandra A. Chaikovshaya; Tatiana E. Terikovska; Tamara N. Kudrya; Aleksandr M. Pinchuk
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 177 KB
- Volume
- 10
- Category
- Article
- ISSN
- 1042-7163
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β¦ Synopsis
C-Phosphorylation of 2,5-dimethylpyrroles with phosphorus (III) halides has been studied. Synthetic methods have been elaborated that provide an access to 3-phosphorylated 2,5-dimethylpyrroles, including pyrrole-substituted halogeno and dihalogeno phosphines; on this basis, a variety of trivalent and pentavalent phosphorus derivatives has been obtained. Ortho-diphosphorylated 2,5-dimethyl-N-arylpyrrole derivatives have been synthesized for the first time.
π SIMILAR VOLUMES
## Abstract Phosphorylation of Nβarylpyrroles with phosphorus tribromide proceeds regioselectively at the position 2 of the heterocyclic system. A 2βtoβ3 migration of the dibromophosphino group has been discovered, with its ease depending on the electronic nature of a substituent on the phenyl ring
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