1. For general reviews: (a) Trost, B. M.; Verhoeven, T. R.ComprehensiveOrganometallic Chemistry; Wilkinson, G., Stone, F. G. A., Abel, E. W., Eds.; Pergamon Press: New York, 1982; Vol. 8, p 799. (b) Heck, R. F.PalladiumReagents in Organic Synthesis, Academic Press: London, 1987; p 117. (c) Tsuji, J.Palladium Reagents and Catalysts, John Wiley & Sons: Chichester, 1995; p 290. (d) Trost, B. M.Angew. Chem.1995,107, 285;Angew. Chem.Int. Ed. Engl.1995,34, 259.
2. Neutral alkylations via palladium(0) catalysis
3. Allylic carbonates. Efficient allylating agents of carbonucleophiles in palladium-catalyzed reactions under neutral conditions
4. Measurement of the secondary hydrogen-deuterium isotope effect in atom transfer reactions of the 1,1-dideuterioallyl radical