John D. Elliott

Asymmetric synthesis via acetal templates. 3. On the stereochemistry observed in the cyclization of chiral acetals of polyolefinic aldehydes; formation of optically active homoallylic alcohols

Paul A. Bartlett, William S. Johnson, John D. Elliott · Journal of the American Chemical Society · 1983 · 172 citations

Novel Organocatalysts, Engineering, Alkene Metathesis +11

The selective endothelin ETA receptor antagonist BQ123 antagonizes endothelin-1-mediated mitogenesis

Eliot H. Ohlstein, Anthony J. Arleth, Heidemarie G. Bryan et al. · European Journal of Pharmacology Molecular Pharmacology · 1992 · 144 citations

Inflammation, Signal Transduction, Allergy +7

1,3-Diarylindan-2-carboxylic Acids, Potent and Selective Non-Peptide Endothelin Receptor Antagonists

John D. Elliott, M. Amparo Lago, Russell D. Cousins et al. · Journal of Medicinal Chemistry · 1994 · 127 citations · Full text

Altmetric Attention Score, Peptide Science, Pharmacotherapy +18

Synthesis and properties of a series of sterically hindered guanidine bases

Derek H. R. Barton, John D. Elliott, Stephen D. Géro · Journal of the Chemical Society Perkin Transactions 1 · 1982 · 113 citations

Combinatorial Chemistry, Diversity Oriented Synthesis, Pentaisopropylguanidine Combine Ease +10

Asymmetric synthesis via chiral acetal templates. 7. Further studies on the cyanation reaction. The use of acetals derived from diols with one chiral center

V. M. F. CHOI, John D. Elliott, William S. Johnson · Tetrahedron Letters · 1984 · 81 citations

Engineering, Chiral Acetal Templates, Chiral Center +7