## Abstract The investigation concerns the effect of a bulky substituent at the pyrrole nitrogen atom on the orientation and regioselectivity of pyrrole phosphorylation with phosphorus(III) halides. As shown, phosphorylation of N‐iso‐propylpyrrole with phosphorus tribromide or trichloride proceeds
C-Phosphorylated pyrazoles. Reaction of N-methyl- and N-phenylpyrazoles with phosphorus(III) halides
✍ Scribed by Andrew A. Tolmachev; Anzhelika I. Sviridon; Alexander N. Kostyuk; Alexander M. Pinchuk
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 738 KB
- Volume
- 6
- Category
- Article
- ISSN
- 1042-7163
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✦ Synopsis
The reactions of N-methyl-and N-phenylpyrazole derivatives with phosphorus(ll1) halides have been studied. The preparative method for synthesis of a variety of 4-phosphorylated pyrazoles, including pyrazolyl substituted halo-and dihalophosphines, has been elaborated. Migration of an alkyl group from 0 to P(III) in 4-phosphorylated 5-alkoxypyrazoles was found to give a P-ylides in a vinylogous manner with respect to the Arbuzov reaction.
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## Abstract For Abstract see ChemInform Abstract in Full Text.