Kristian Kather

1,3-Allylic Strain as a Control Element in the Paternò−Büchi Reaction of Chiral Silyl Enol Ethers:  Synthesis of Diastereomerically Pure Oxetanes Containing Four Contiguous Stereogenic Centers

Thorsten Bach, Kai Jödicke, Kristian Kather et al. · Journal of the American Chemical Society · 1997 · 56 citations

Asymmetric Catalysis, Chemical Engineering, Cross-coupling Reaction +14

Synthesis of Five-, Six-, and Seven-Membered Heterocycles by Intramolecular Ring Opening Reactions of 3-Oxetanol Derivatives

Thorsten Bach, Kristian Kather, Oliver H. Krämer · The Journal of Organic Chemistry · 1998 · 54 citations

Engineering, Heterocyclic, 3-Oxetanol Derivatives +13

High Helicities of Lys-Containing, Ala-Rich Peptides Are Primarily Attributable to a Large, Context-Dependent Lys Stabilization

Lawrence J. Williams, Kristian Kather, D. S. KEMP · Journal of the American Chemical Society · 1998 · 39 citations

Peptide Engineering, Molecular Biology, Peptide Science +18

Facial Diastereoselectivity in the Paternò–Büchi Reaction of Chiral Silyl Enol Ethers

Thorsten Bach, Kai Jödicke, Kristian Kather et al. · Angewandte Chemie International Edition in English · 1995 · 28 citations

Asymmetric Catalysis, Stereogenic Centers, Engineering +14

Intramolecular Nucleophilic Substitution at the C-4 Position of Functionalized Oxetanes:  A Ring Expansion for the Construction of Various Heterocycles

Thorsten Bach, Kristian Kather · The Journal of Organic Chemistry · 1996 · 27 citations

Ring Expansion, Engineering, Heterocyclic +11