Use of Thallium(I) Ethoxide in Suzuki Cross Coupling Reactions
Organic Letters2000Vol. 2(17), pp. 2691–2694
Citations Over TimeTop 10% of 2000 papers
Abstract
[reaction: see text]Thallium(I) ethoxide promotes Suzuki cross couplings for a range of vinyl- and arylboronic acids with vinyl and aryl halide partners in good to excellent yields. This reagent offers distinct advantages over thallium(I) hydroxide in terms of commercial availability, stability, and ease of use.
Related Papers
- Thallium in the environment(1998)
- → Reactions of complexes of gold(I) with bis(pentafluorophenyl)thallium(III) halides(1974)29 cited
- Penicillamine produces changes in the acute blood elimination and tissue accumulation of thallium.(1995)
- → Sequential oxidimetric determination of thallium(I) and (III)(1969)24 cited
- → Thallium and Thallium Compounds(2000)2 cited