J.‐R. SCHWARK

Aldotetroses and C(3)-Modified Aldohexoses as Substrates for N-Acetylneuraminic Acid Aldolase: A Model for the Explanation of the Normal and the Inversed Stereoselectivity

Wolfgang Fitz, J.‐R. SCHWARK, Chi‐Huey Wong · The Journal of Organic Chemistry · 1995 · 66 citations

Bioorganic Chemistry, Aldo-keto Reductase, Glycobiology +18

Metallated 2-alkenyl carbamates: chiral homoenolate reagents for asymmetric synthesis

D. HOPPE, Thomas Krämer, J.‐R. SCHWARK et al. · Pure and Applied Chemistry · 1990 · 55 citations · Full text

Organic Chemistry, Chiral Homoenolate Reagents, Chemistry +2

Enantiomerically enriched allystannanes from chiral allyllithium derivatives and their highly regio-, diastereo- and enantioselective hydroxyalkylation

Thomas Krämer, J.‐R. SCHWARK, Dieter Hoppe · Tetrahedron Letters · 1989 · 54 citations

Engineering, Chiral Allyllithium Derivatives, Enantioselective Hydroxyalkylation +7

Enantiomerically enriched 1-(N,N-diisopropylcarbamoyloxy)-1,3-dimethylallyllithium: stereochemistry of the stannylation, titanation, and the homoaldol reaction

Oliver Zschage, J.‐R. SCHWARK, Thomas Krämer et al. · Tetrahedron · 1992 · 52 citations

Engineering, Biochemistry, Natural Sciences +8

Preparation of an Enantiomerically Enriched Allyllithium Derivative by Deprotonation with Kinetic Resolution of Enantiomers

Oliver Zschage, J.‐R. SCHWARK, Dieter Hoppe · Angewandte Chemie International Edition in English · 1990 · 51 citations

Engineering, Kinetic Resolution, Racemic Carbonate 1 +9