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C-phosphorylation of n-methylpyrrole

✍ Scribed by Sergey P. Ivonin; Tetjana E. Terikovska; Alexandra A. Chaikovskaya; Anatoliy P. Marchenko; Georgiy N. Koydan; Alexander M. Pinchuk; Andrew A. Tolmachev


Publisher
John Wiley and Sons
Year
1999
Tongue
English
Weight
190 KB
Volume
10
Category
Article
ISSN
1042-7163

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✦ Synopsis


The phosphorylation of N-methylpyrrole with phosphorus (III) halides has been studied. Migration of the dibromophosphino group from the second to the third position of N-methylpyrrole, leading to the 3-dibromophosphine, has been found. Methods for the synthesis of 2,4-bisphosphorylated pyrroles have been developed.


πŸ“œ SIMILAR VOLUMES


C-phosphorylation of N-arylpyrroles
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## Abstract Phosphorylation of N‐arylpyrroles with phosphorus tribromide proceeds regioselectively at the position 2 of the heterocyclic system. A 2‐to‐3 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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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 an

18F-labelling of thiophene and N-methylp
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## Abstract 2‐ and 3‐[^18^F]fluorothiophene and 2‐ and 3 [^18^F]fluoro‐N‐methyl pyrrole have been obtained by the reaction of thiophene and N‐methylpyrrole with molecular fluorine [^18^F]‐F~2~ under carefully controlled conditions.