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Cite the Following Article
A superior P-H phosphonite: Asymmetric allylic substitutions with fenchol-based palladium catalysts
Bernd Goldfuss, Thomas Löschmann, Tina Kop-Weiershausen, Jörg Neudörfl and Frank Rominger
Beilstein J. Org. Chem. 2006, 2, No. 7.
https://doi.org/10.1186/1860-5397-2-7
How to Cite
Goldfuss, B.; Löschmann, T.; Kop-Weiershausen, T.; Neudörfl, J.; Rominger, F. Beilstein J. Org. Chem. 2006, 2, No. 7. doi:10.1186/1860-5397-2-7
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Scholarly Works
- Brüllingen, E.; Neudörfl, J.-M.; Goldfuss, B. Ligand's electronegativity controls the sense of enantioselectivity in BIFOP-X palladium-catalyzed allylic alkylations. New Journal of Chemistry 2019, 43, 15743–15753. doi:10.1039/c9nj02798j
- Brüllingen, E.; Neudörfl, J.-M.; Goldfuss, B. Enantioselective Cu-catalyzed 1,4-additions of organozinc and Grignard reagents to enones: exceptional performance of the hydrido-phosphite-ligand BIFOP-H. New Journal of Chemistry 2019, 43, 4787–4799. doi:10.1039/c8nj05886e
- Fox, F.; Neudörfl, J. M.; Goldfuss, B. Silanediol versus chlorosilanol: hydrolyses and hydrogen-bonding catalyses with fenchole-based silanes. Beilstein journal of organic chemistry 2019, 15, 167–186. doi:10.3762/bjoc.15.17
- Trillo, R. B.; Neudörfl, J. M.; Goldfuss, B. An unusually stable chlorophosphite: What makes BIFOP-Cl so robust against hydrolysis?. Beilstein journal of organic chemistry 2015, 11, 313–322. doi:10.3762/bjoc.11.36
- Lai, Z.-W.; Yang, R.-F.; Ye, K.-Y.; Sun, H.; You, S.-L. Synthesis of 1-[bis(trifluoromethyl)phosphine]-1’-oxazolinylferrocene ligands and their application in regio- and enantioselective Pd-catalyzed allylic alkylation of monosubstituted allyl substrates. Beilstein journal of organic chemistry 2014, 10, 1261–1266. doi:10.3762/bjoc.10.126
- Trillo, R. B.; Leven, M.; Neudörfl, J. M.; Goldfuss, B. Electronegativity Governs Enantioselectivity: Alkyl-Aryl Cross-Coupling with Fenchol-Based Palladium-Phosphorus Halide Catalysts. Advanced Synthesis & Catalysis 2012, 354, 1451–1465. doi:10.1002/adsc.201100924
- Gliga, A.; Goldfuss, B.; Neudörfl, J. M. Lithium phosphonate umpolung catalysts: Do fluoro substituents increase the catalytic activity?. Beilstein journal of organic chemistry 2011, 7, 1189–1197. doi:10.3762/bjoc.7.138
- Gliga, A.; Klare, H.; Schumacher, M.; Soki, F.; Neudörfl, J. M.; Goldfuss, B. New Umpolung Catalysts: Reactivity and Selectivity of Terpenol-Based Lithium Phosphonates in Enantioselective Benzoin-Type Couplings†. European Journal of Organic Chemistry 2010, 2011, 256–263. doi:10.1002/ejoc.201001295
- Leven, M.; Schlörer, N.; Neudörfl, J. M.; Goldfuss, B. Control of enantioselectivity with flexible biaryl axes: terpene-based alkylzinc catalysts in enantioselective dialkylzinc additions. Chemistry (Weinheim an der Bergstrasse, Germany) 2010, 16, 13443–13449. doi:10.1002/chem.201001106
- Alpagut, Y.; Goldfuss, B.; Neudörfl, J.-M. Control of asymmetric biaryl conformations with terpenol moieties: syntheses, structures and energetics of new enantiopure C2-symmetric diols. Beilstein journal of organic chemistry 2008, 4, 25. doi:10.3762/bjoc.4.25
- Soki, F.; Neudörfl, J.-M.; Goldfuss, B. Homo- vs. heterometallic organoaluminum fencholates: Structures and selectivities. Journal of Organometallic Chemistry 2008, 693, 2139–2146. doi:10.1016/j.jorganchem.2008.03.013
- Lange, D. A.; Goldfuss, B. Electronic differentiation competes with transition state sensitivity in palladium-catalyzed allylic substitutions. Beilstein journal of organic chemistry 2007, 3, 36. doi:10.1186/1860-5397-3-36
