Cite the Following Article
Electronic differentiation competes with transition state sensitivity in palladium-catalyzed allylic substitutions
Dominik A. Lange and Bernd Goldfuss
Beilstein J. Org. Chem. 2007, 3, No. 36.
https://doi.org/10.1186/1860-5397-3-36
How to Cite
Lange, D. A.; Goldfuss, B. Beilstein J. Org. Chem. 2007, 3, No. 36. doi:10.1186/1860-5397-3-36
Download Citation
Citation data can be downloaded as file using the "Download" button or used for copy/paste from the text window
below.
Citation data in RIS format can be imported by all major citation management software, including EndNote,
ProCite, RefWorks, and Zotero.
Citations to This Article
Up to 20 of the most recent references are displayed here.
Scholarly Works
- Hausoul, P. J. C.; Lutz, M.; Jastrzebski, J. T. B. H.; Bruijnincx, P. C. A.; Weckhuysen, B. M.; Gebbink, R. J. M. K. Mechanistic Study of the Pd/TOMPP-Catalyzed Telomerization of 1,3-Butadiene: Influence of Aromatic Solvents on Bis-Phosphine Complex Formation and Regioselectivity. Organometallics 2013, 32, 5047–5057. doi:10.1021/om400246a
- Poli, G.; Prestat, G.; Liron, F.; Kammerer-Pentier, C. Selectivity in Palladium-Catalyzed Allylic Substitution. Topics in Organometallic Chemistry; Springer Berlin Heidelberg, 2011; Vol. 43, pp 1–63. doi:10.1007/3418_2011_14
- Milhau, L.; Guiry, P. J. Palladium-Catalyzed Enantioselective Allylic Substitution. Topics in Organometallic Chemistry; Springer Berlin Heidelberg, 2011; Vol. 43, pp 95–153. doi:10.1007/3418_2011_9
- Bottari, G.; Meduri, A.; Drommi, D.; Brancatelli, G.; Faraone, F. Synthesis, Coordination Properties and Application of New N,N‐Ligands Based on Bornyl and Binaphthylazepine Chiral Backbones in Palladium‐Catalyzed Allylic Substitution Reactions. European Journal of Inorganic Chemistry 2011, 2011, 2738–2745. doi:10.1002/ejic.201100113
- Panossian, A.; Fernández-Pérez, H.; Popa, D.; Vidal-Ferran, A. Highly modular P-OP ligands in asymmetric allylic substitution. Tetrahedron: Asymmetry 2010, 21, 2281–2288. doi:10.1016/j.tetasy.2010.08.004