Franz J. Weiberth

Key Green Chemistry research areas from a pharmaceutical manufacturers’ perspective revisited

Marian C. Bryan, Peter J. Dunn, David A. Entwistle et al. · Green Chemistry · 2018 · 582 citations · Full text

Engineering, Chemical Transformation, Green Chemistry +18

Copper(I)-activated addition of Grignard reagents to nitriles. Synthesis of ketimines, ketones, and amines

Franz J. Weiberth, Stan S. Hall · The Journal of Organic Chemistry · 1987 · 113 citations

Chemical Engineering, Engineering, Chemical Analysis +12

Alkylation-reduction of carbonyl systems. Part 14. Tandem alkylation-reduction. Highly stereoselective synthesis of (E)-1-hydroxymethyl methyl propenyl ethers from aldehydes using 1-lithio-1-methoxyallene

Franz J. Weiberth, Stan S. Hall · The Journal of Organic Chemistry · 1985 · 42 citations

Highly Stereoselective Synthesis, Chemical Engineering, Engineering +10

Demonstration on Pilot-Plant Scale of the Utility of 1,5,7-Triazabicyclo[4.4.0]dec-5-ene (TBD) as a Catalyst in the Efficient Amidation of an Unactivated Methyl Ester

Franz J. Weiberth, Yong Yu, Witold Subotkowski et al. · Organic Process Research & Development · 2012 · 41 citations

Bioorganic Chemistry, Engineering, H-pgds Inhibitor +17

Chemical Development of MDL 103371:  An <i>N</i>-Methyl-<scp>d</scp>-Aspartate-Type Glycine Receptor Antagonist for the Treatment of Stroke

Timothy Watson, Stephen W. Horgan, Ramnik S. Shah et al. · Organic Process Research & Development · 2000 · 35 citations

Pharmaceutical Science, Chemical Development, Mdl 103371 +16