8 article(s) from Goldfuss, Bernd
The enzyme mechanism of patchoulol synthase
- Houchao Xu,
- Bernd Goldfuss,
- Gregor Schnakenburg and
- Jeroen S. Dickschat
Beilstein J. Org. Chem. 2022, 18, 13–24, doi:10.3762/bjoc.18.2
Silanediol versus chlorosilanol: hydrolyses and hydrogen-bonding catalyses with fenchole-based silanes
- Falco Fox,
- Jörg M. Neudörfl and
- Bernd Goldfuss
Beilstein J. Org. Chem. 2019, 15, 167–186, doi:10.3762/bjoc.15.17
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, doi:10.3762/bjoc.11.36
New hydrogen-bonding organocatalysts: Chiral cyclophosphazanes and phosphorus amides as catalysts for asymmetric Michael additions
- Helge Klare,
- Jörg M. Neudörfl and
- Bernd Goldfuss
Beilstein J. Org. Chem. 2014, 10, 224–236, doi:10.3762/bjoc.10.18
Metal-mediated aminocatalysis provides mild conditions: Enantioselective Michael addition mediated by primary amino catalysts and alkali-metal ions
- Matthias Leven,
- Jörg M. Neudörfl and
- Bernd Goldfuss
Beilstein J. Org. Chem. 2013, 9, 155–165, doi:10.3762/bjoc.9.18
Lithium phosphonate umpolung catalysts: Do fluoro substituents increase the catalytic activity?
- Anca Gliga,
- Bernd Goldfuss and
- Jörg M. Neudörfl
Beilstein J. Org. Chem. 2011, 7, 1189–1197, doi:10.3762/bjoc.7.138
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, doi:10.1186/1860-5397-3-36
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, doi:10.1186/1860-5397-2-7
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