Cite the Following Article
An unusually stable chlorophosphite: What makes BIFOP–Cl so robust against hydrolysis?
Roberto Blanco Trillo, Jörg M. Neudörfl and Bernd Goldfuss
Beilstein J. Org. Chem. 2015, 11, 313–322.
https://doi.org/10.3762/bjoc.11.36
How to Cite
Blanco Trillo, R.; Neudörfl, J. M.; Goldfuss, B. Beilstein J. Org. Chem. 2015, 11, 313–322. doi:10.3762/bjoc.11.36
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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
- 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
