Joseph E. Lynch

Asymmetric syntheses based on 1,3-oxathianes. 2. Synthesis of chiral tertiary .alpha.-hydroxy aldehydes, .alpha.-hydroxy acids, glycols [R1R2C(OH)CH2OH], and carbinols [R1R2C(OH)Me] in high enantiomeric purity.

Joseph E. Lynch, Ernest L. Eliel · Journal of the American Chemical Society · 1984 · 144 citations

Asymmetric Syntheses, Engineering, Biochemistry +15

Mechanism of an acid chloride-imine reaction by low-temperature FT-IR: .beta.-lactam formation occurs exclusively through a ketene intermediate

Joseph E. Lynch, Stephen M. Riseman, William L. Laswell et al. · The Journal of Organic Chemistry · 1989 · 108 citations

Molecular Sciences, Ketene Intermediate, Engineering +14

An enantiocontrolled cycloaddition approach to (+)-brefeldin A

Barry M. Trost, Joseph E. Lynch, Patrice Renaut et al. · Journal of the American Chemical Society · 1986 · 104 citations

Quantitative Methods, Engineering, Databases +18

Synthesis of a Muscarinic Receptor Antagonist via a Diastereoselective Michael Reaction, Selective Deoxyfluorination and Aromatic Metal−Halogen Exchange Reaction

Toshiaki Mase, Ioannis N. Houpis, Atsushi Akao et al. · The Journal of Organic Chemistry · 2001 · 92 citations

A chemical synthesis of nicotinamide adenine dinucleotide (NAD+)

Jaemoon Lee, Hywyn Churchil, Woo‐Baeg Choi et al. · Chemical Communications · 1999 · 74 citations

Nicotinamide Mononucleotide, Practical Synthesis, Bioorganic Chemistry +8