Eugene A. Terefenko

发表

Synthesis and activity of novel 1- or 3-(3-amino-1-phenyl propyl)-1,3-dihydro-2H-benzimidazol-2-ones as selective norepinephrine reuptake inhibitors.

E. Koury, D. Deecher, P. Mahaney, 2008, Bioorganic & medicinal chemistry letters.

The reaction of o-amino aryl carboxylic acids with Grignard reagents. The unusual effect of the N-protecting group on aryl ketone formation

Eugene A. Terefenko, Puwen Zhang, E. Terefenko, 2001 .

1- or 3-(3-Amino-2-hydroxy-1-phenyl propyl)-1,3-dihydro-2H-benzimidazol-2-ones: potent, selective, and orally efficacious norepinephrine reuptake inhibitors.

D. Deecher, P. Mahaney, E. Trybulski, 2009, Journal of medicinal chemistry.

Synthesis and activity of novel 1- or 3-(3-amino-1-phenyl propyl)-1,3-dihydro-2H-benzimidazol-2-ones as selective norepinephrine reuptake inhibitors.

D. Deecher, P. Mahaney, E. Trybulski, 2008, Bioorganic & Medicinal Chemistry Letters.

3-(Arylamino)-3-phenylpropan-2-olamines as a new series of dual norepinephrine and serotonin reuptake inhibitors.

D. Deecher, P. Mahaney, E. Trybulski, 2009, Bioorganic & medicinal chemistry letters.

SAR studies of 6-(arylamino)-4,4-disubstituted-1-methyl-1,4-dihydro-benzo[d][1,3]oxazin-2-ones as progesterone receptor antagonists.

R. Winneker, Eugene A. Terefenko, J. Wrobel, 2007, Bioorganic & Medicinal Chemistry Letters.

Novel 6-aryl-1,4-dihydrobenzo[d]oxazine-2-thiones as potent, selective, and orally active nonsteroidal progesterone receptor agonists.

R. Winneker, Eugene A. Terefenko, J. Wrobel, 2003, Bioorganic & medicinal chemistry letters.

6-Aryl-1,4-dihydro-benzo[d][1,3]oxazin- 2-ones: a novel class of potent, selective, and orally active nonsteroidal progesterone receptor antagonists.

R. Winneker, S. Lundeen, Eugene A. Terefenko, 2002, Journal of medicinal chemistry.

Synthesis and progesterone receptor antagonist activities of 6-aryl benzimidazolones and benzothiazolones.

Z. Zhang, P. Zhang, Eugene A. Terefenko, 2001, Bioorganic & medicinal chemistry letters.