B. E. Segelstein

A Mild Method for the Preparation of 1,3,4-Oxadiazoles: Triflic Anhydride Promoted Cyclization of Diacylhydrazines

S. Liras, M. Allen, B. E. Segelstein, 2000 .

Biaryl piperidines as potent and selective delta opioid receptor ligands.

Anne W. Schmidt, S. Liras, Ernesto Callegari, 2010, Bioorganic & medicinal chemistry letters.

Ethoxymethylenemalonates and Malononitriles (EMM reagents) as formic acid equivalents: Synthesis of fused-imidazoles under neutral or mildly acidic con

J. Macor, B. Chenard, B. E. Segelstein, 1993 .

Expanding the medicinal chemistry toolbox: stereospecific generation of methyl group-containing propylene linkers

J. Marineau, A. Fliri, R. Volkmann, 2006 .

Equilibration of the Oxidative Addition Product of Tetrakis(triphenylphosphine)palladium and Electron-Rich Aryl Halides Leads to Product Scrambling in the Stille Reaction

B. Chenard, T. Butler, B. E. Segelstein, 1995 .

Design, synthesis and biological evaluation of 3-amino-3-phenylpropionamide derivatives as novel mu opioid receptor ligands.

J. Blake, S. Liras, S. Mclean, 2000, Bioorganic & medicinal chemistry letters.

Discovery and pharmacological characterization of a selective delta opiate receptor antagonist (CP-646,777)

Anne W. Schmidt, S. Liras, Ernesto Callegari, 2011 .

(3R,4S)-3-[4-(4-fluorophenyl)-4-hydroxypiperidin-1-yl]chroman-4,7-diol: a conformationally restricted analogue of the NR2B subtype-selective NMDA antagonist (1S,2S)-1-(4-hydroxyphenyl)-2-(4-hydroxy-4-phenylpiperidino)- 1-propanol.

F. Menniti, J. Blake, W. White, 1998, Journal of medicinal chemistry.