B. Dyck

发表

Studies on the structure-activity relationship of bicifadine analogs as monoamine transporter inhibitors.

Beth A. Fleck, Rebecca R. Pick, Mingzhu Zhang, 2008, Bioorganic & medicinal chemistry letters.

Composés capables de moduler le calcium intracellulaire

B. Dyck, J. Grey, Jianguo Cao, 2011 .

Design and synthesis of tricyclic corticotropin-releasing factor-1 antagonists.

Zhiqian Guo, D. Grigoriadis, S. Hoare, 2005, Journal of medicinal chemistry.

Studies Directed toward the Total Synthesis of Cerorubenic Acid-III. 5. A Radical Cyclization Route Leading to the Methyl Ester of the Natural Isomer1

B. Dyck, L. Paquette, 1998 .

Aryl piperazine melanocortin MC4 receptor agonists.

Teresa Y. Phillips, B. Dyck, M. Cismowski, 2003, Bioorganic & medicinal chemistry letters.

Unexpected formation of 1,3-diselenetanes from the reaction of camphor enolate with selenium

B. Dyck, M. Parvez, T. G. Back, 1994 .

A Novel Camphor-Derived Selenenamide That Acts as a Glutathione Peroxidase Mimetic

B. Dyck, T. G. B. and, 1997 .

Potent imidazole and triazole CB1 receptor antagonists related to SR141716.

Teresa Y. Phillips, Brock T Brown, B. Dyck, 2004, Bioorganic & medicinal chemistry letters.

Design and Synthesis of Tricyclic Imidazo[4,5- b ]pyridin-2-ones as Corticotropin-Releasing Factor-1 Antagonists

Zhiqian Guo, D. Grigoriadis, B. Dyck, 2005 .

Potent, orally active corticotropin-releasing factor receptor-1 antagonists containing a tricyclic pyrrolopyridine or pyrazolopyridine core.

Zhiqian Guo, D. Grigoriadis, B. Dyck, 2005, Journal of medicinal chemistry.

Asymmetric electrophilic methoxyselenenylations and cyclizations with 3-camphorseleno derivatives

B. Dyck, T. G. Back, Siqiao Nan, 1999 .

1,3-Diselenetanes and 1,3-Dithietanes Derived from Camphor. Formation, Structure, Stereochemistry, and Oxidation to Selenoxide and Sulfoxide Products

B. Dyck, M. Parvez, T. G. Back, 1995 .

Potent and orally active non-peptide antagonists of the human melanocortin-4 receptor based on a series of trans-2-disubstituted cyclohexylpiperazines.

Beth A. Fleck, M. Joppa, B. Dyck, 2005, Bioorganic & medicinal chemistry letters.

FORMATION OF THE TRANSIENT TELLUROKETONE (1R)-3-TELLUROXOCAMPHOR AND ITS DIMERIZATION TO THE CORRESPONDING SYN- AND ANTI-1,3-DITELLURETANES

B. Dyck, M. Parvez, T. G. Back, 1995 .

Total asymmetric synthesis of the putative structure of the cytotoxic diterpenoid (-)-sclerophytin a and of the authentic natural sclerophytins A and B.

D. Friedrich, B. Dyck, O. Moradei, 2001, Journal of the American Chemical Society.

[3aR‐(3aα,4α,7α,7aα)]‐2‐Acetyl‐4,8,8‐trimethylperhydro‐4,7‐methano‐1,2‐benzisoselenazol‐3a‐ol

B. Dyck, M. Parvez, T. G. Back, 1998 .

Characterization of thien-2-yl 1S,2R-milnacipran analogues as potent norepinephrine/serotonin transporter inhibitors for the treatment of neuropathic pain.

Beth A. Fleck, Rebecca R. Pick, M. Bradbury, 2008, Journal of medicinal chemistry.

Identification of 1S,2R-milnacipran analogs as potent norepinephrine and serotonin transporter inhibitors.

Beth A. Fleck, Mingzhu Zhang, F. Jovic, 2008, Bioorganic & medicinal chemistry letters.

Substituted chromones and quinolones as potent melanin-concentrating hormone receptor 1 antagonists.

B. Dyck, Junko Tamiya, C. Heise, 2006, Bioorganic & medicinal chemistry letters.

The synthesis of some novel N-chloro-Δ1-4-azasteroids by efficient N-chlorination of azasteroid lactams with trichloroisocyanuric acid

B. Dyck, T. G. Back, J. H. Chau, 1991 .

A short synthesis of the antifungal principle of Sapium japonicum

B. Dyck, T. G. Back, 1992 .

Bis(aminopyrrolidine)-derived ureas (APUs) as potent MCH1 receptor antagonists.

John Saunders, Liren Zhao, Mingzhu Zhang, 2005, Bioorganic & medicinal chemistry letters.

Solvent-Controlled, Site-Selective N-Alkylation Reactions of Azolo-Fused Ring Heterocycles at N1-, N2-, and N3-Positions, Including Pyrazolo[3,4- d]pyrimidines, Purines, [1,2,3]Triazolo[4,5]pyridines, and Related Deaza-Compounds.

P. Stańczak, B. Dyck, A. Rheingold, 2018, The Journal of organic chemistry.

Discovery of Selective Phosphodiesterase 1 Inhibitors with Memory Enhancing Properties.

M. Augustin, C. Allerston, Iriny Botrous, 2017, Journal of medicinal chemistry.

Phosphodiesterase 1b (PDE1B) Regulates Spatial and Contextual Memory in Hippocampus

K. Baumgärtel, S. Xia, B. Dyck, 2019, Front. Mol. Neurosci..

Synthesis and structure-activity relationships of biarylcarboxamide bis-aminopyrrolidine urea derived small-molecule antagonists of the melanin-concentrating hormone receptor-1 (MCH-R1).

John Saunders, Liren Zhao, D. Provencal, 2005, Bioorganic & medicinal chemistry letters.

Thienopyrimidinone bis-aminopyrrolidine ureas as potent melanin-concentrating hormone receptor-1 (MCH-R1) antagonists.

Mingzhu Zhang, Troy D. Vickers, B. Dyck, 2007, Bioorganic & medicinal chemistry letters.

Small molecule melanin‐concentrating hormone receptor 1 (MCH1R) antagonists as anxiolytic and antidepressive agents

B. Dyck, 2005 .

Studies on a series of milnacipran analogs containing a heteroaromatic group as potent norepinephrine and serotonin transporter inhibitors.

Beth A. Fleck, Mingzhu Zhang, F. Jovic, 2008, Bioorganic & medicinal chemistry letters.

Design and synthesis of tricyclic imidazo[4,5-b]pyridin-2-ones as corticotropin-releasing factor-1 antagonists.

Zhiqian Guo, D. Grigoriadis, B. Dyck, 2005, Journal of Medicinal Chemistry.

Synthesis and structure-activity relationships of retro bis-aminopyrrolidine urea (rAPU) derived small-molecule antagonists of the melanin-concentrating hormone receptor-1 (MCH-R1). Part 1.

Mingzhu Zhang, Troy D. Vickers, B. Dyck, 2006, Bioorganic & medicinal chemistry letters.

Characterization of thien-2-yl 1S,2R-milnacipran analogues as potent norepinephrine/serotonin transporter inhibitors for the treatment of neuropathic pain.

Beth A. Fleck, Rebecca R. Pick, M. Bradbury, 2008, Journal of Medicinal Chemistry.

Studies on the SAR and pharmacophore of milnacipran derivatives as monoamine transporter inhibitors.

M. Mesleh, Beth A. Fleck, Mingzhu Zhang, 2008, Bioorganic & medicinal chemistry letters.