Hermann Bergmann

Highly Enantioselective Intra- and Intermolecular [2 + 2] Photocycloaddition Reactions of 2-Quinolones Mediated by a Chiral Lactam Host:  Host−Guest Interactions, Product Configuration, and the Origin of the Stereoselectivity in Solution

Thorsten Bach, Hermann Bergmann, Benjamin Grosch et al. · Journal of the American Chemical Society · 2002 · 190 citations

Enantioselective Intra-, Solution Phase Photochemistry, Nmr Titration Experiments +15

Enantioselective Intramolecular [2+2]-Photocycloaddition Reactions in Solution

Thorsten Bach, Hermann Bergmann, Klaus Harms · Angewandte Chemie International Edition · 2000 · 128 citations

Prochiral 2-Quinolones, Engineering, Heterocyclic +15

Enantioselective Intermolecular [2 + 2]-Photocycloaddition Reactions of Alkenes and a 2-Quinolone in Solution

Thorsten Bach, Hermann Bergmann · Journal of the American Chemical Society · 2000 · 98 citations

Heterocyclic, Photoredox Process, Biochemistry +10

High Facial Diastereoselectivity in the Photocycloaddition of a Chiral Aromatic Aldehyde and an Enamide Induced by Intermolecular Hydrogen Bonding

Thorsten Bach, Hermann Bergmann, Klaus Harms · Journal of the American Chemical Society · 1999 · 79 citations

Enamide Induced, Engineering, Photochemistry +13

The [2+2]-Photocycloaddition of Aromatic Aldehydes and Ketones to 3,4-Dihydro-2-pyridones: Regioselectivity, Diastereoselectivity, and Reductive Ring Opening of the Product Oxetanes

Thorsten Bach, Hermann Bergmann, Harm Brummerhop et al. · Chemistry - A European Journal · 2001 · 66 citations