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Reactions of triarylphosphines with organolithium reagents. Formation of biaryls

Reactions of triarylphosphines with organolithium reagents. Formation of biaryls Triarylphosphines bearing 2‐pyridyl or 2‐benzothiazyl groups react with organolithium reagents at −78°C in THF to afford both coupling products and ligand exchanged triarylphosphines. The ligand coupling and ligand exchange are considered to take place via an intermediate formed by the nucleophilic attack of a lithium reagent on the phosphorus atom. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Heteroatom Chemistry Wiley

Reactions of triarylphosphines with organolithium reagents. Formation of biaryls

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References (8)

Publisher
Wiley
Copyright
Copyright © 1993 Wiley Subscription Services
ISSN
1042-7163
eISSN
1098-1071
DOI
10.1002/hc.520040503
Publisher site
See Article on Publisher Site

Abstract

Triarylphosphines bearing 2‐pyridyl or 2‐benzothiazyl groups react with organolithium reagents at −78°C in THF to afford both coupling products and ligand exchanged triarylphosphines. The ligand coupling and ligand exchange are considered to take place via an intermediate formed by the nucleophilic attack of a lithium reagent on the phosphorus atom.

Journal

Heteroatom ChemistryWiley

Published: Jan 1, 1993

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