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ChemInform Abstract: Water Soluble Phosphanes. Part 9. Nucleophilic Phosphanylation of Fluoroaromatic Compounds with Carboxyl, Carboxymethyl, and Aminomethyl Functionalities — An Efficient Synthetic Route to Amphiphilic Arylphosphanes.

✍ Scribed by M. HINGST; M. TEPPER; O. STELZER

Book ID: 101867562
Publisher: John Wiley and Sons
Year: 2010
Weight: 34 KB
Volume: 29
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.199814148

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✦ Synopsis

In continuation of a work to develop water-soluble phosphanes for two-phase catalysis, nucleophilic phosphanylations of potassium or lithium salts of fluoroaromatic compounds are carried out. Ligands such as (III)-(VI) and (VIII) and (X) are characterized by NMR and mass spectroscopy. -(HINGST, M.; TEPPER, M.; STELZER, O.; Eur.

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Nucleophilic Phosphanylation of Fluoroaromatic Compounds with Carboxyl, Carboxymethyl, and Aminomethyl Functionalities − an Efficient Synthetic Route to Amphiphilic Arylphosphanes

✍ Martin Hingst; Michael Tepper; Othmar Stelzer 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 654 KB

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