J. Matasi

发表

Divergent Pathways in the Intramolecular Reactions between Rhodium-Stabilized Vinylcarbenoids and Pyrroles: Construction of Fused Tropanes and 7-Azabicyclo[4.2.0]octadienes

H. Davies, G. Ahmed, J. Matasi, 1996 .

Nociceptin inhibits capsaicin-induced bronchoconstriction in isolated guinea pig lung.

R. Egan, D. Tulshian, M. Corboz, 2000, European journal of pharmacology.

The Anxiolytic-Like Effects of the Novel, Orally Active Nociceptin Opioid Receptor Agonist 8-[bis(2-Methylphenyl)methyl]-3-phenyl-8-azabicyclo[3.2.1]octan-3-ol (SCH 221510)

D. Tulshian, R. Hodgson, M. Graziano, 2008, Journal of Pharmacology and Experimental Therapeutics.

Structure-activity relationships of 2,4-diphenyl-1H-imidazole analogs as CB2 receptor agonists for the treatment of chronic pain.

W. Greenlee, D. Tulshian, K. Cox, 2011, Bioorganic & medicinal chemistry letters.

Relative Asymmetric Induction in the Intramolecular Reaction between Alkynes and Cyclopropylcarbene−Chromium Complexes: Stereocontrolled Synthesis of Five-Membered Rings Fused to Oxygen Heterocycles

Jingbo Yan, Jin Zhu, J. Herndon, 1999 .

Reactions of Cyclopropylcarbene-Chromium Complexes

C. Daitch, J. Herndon, J. Matasi, 1990 .

The discovery and synthesis of novel adenosine receptor (A(2A)) antagonists.

B. Neustadt, Jinsong Hao, D. Tulshian, 2005, Bioorganic & medicinal chemistry letters.

Hydrogenation of vinylogous esters

J. Herndon, J. Matasi, 1992 .

Rhodium(II) catalyzed intramolecular reactions between vinyldiazomethanes and pyrroles. Novel synthesis of fused 7-azabicyclo[4.2.0]octadienes

H. Davies, J. Matasi, 1994 .

Enantioselective Synthesis of Functionalized Tropanes by Rhodium(II) Carboxylate-Catalyzed Decomposition of Vinyldiazomethanes in the Presence of Pyrroles

C. Thornley, H. Davies, A. N. Kong, 1997 .

Synthesis and SAR development of novel P2X7 receptor antagonists for the treatment of pain: part 2.

W. Greenlee, D. Tulshian, R. Bertorelli, 2011, Bioorganic & medicinal chemistry letters.

3H-[1,2,4]-Triazolo[5,1-i]purin-5-amine derivatives as adenosine A2A antagonists.

W. Greenlee, D. Tulshian, E. Ongini, 2007, Bioorganic & medicinal chemistry letters.

Preparation of seven-membered rings by the reaction of cyclopropylcarbene-tungsten and molybdenum complexes with alkynes

J. Herndon, Metin Zora, P. Patel, 1993 .

Bioavailable pyrrolo-benzo-1,4-diazines as Na(v)1.7 sodium channel blockers for the treatment of pain.

D. Tulshian, R. J. Herr, Xianfeng Sun, 2014, Bioorganic & medicinal chemistry letters.

Discovery of pyrrolo-benzo-1,4-diazines as potent Na(v)1.7 sodium channel blockers.

D. Tulshian, R. J. Herr, D. Rindgen, 2014, Bioorganic & medicinal chemistry letters.

Control of carbenoid reactivity through neighboring group participation

C. Thornley, H. Davies, J. Matasi, 1995 .

Potential antidepressant effects of novel tropane compounds, selective for serotonin or dopamine transporters.

I. Lucki, G. Gatto, S. Hemby, 1997, The Journal of pharmacology and experimental therapeutics.

Anti-feedant effects of surface accumulated flavonoids of Polygonum Senegalense

R. W. Mwangi, J. Midiwo, P. Waterman, 1990 .

Synthesis of cyclopentane-fused oxygen heterocycles from the intramolecular reaction of alkynes with cyclopropylcarbene-chromium complexes

J. Herndon, J. Matasi, 1990 .

Alterations in behavior and opioid gene expression induced by the novel tropane analog WF-31.

J. Daunais, L. Porrino, C. Thornley, 1997, Brain research. Molecular brain research.

Effect of carbenoid structure on the reactivity of rhodium-stabilized carbenoids

H. Davies, T. Hansen, D. Stafford, 1998 .

Synthesis of 3β-Aryl-8-azabicyclo(3.2.1)octanes with High Binding Affinities and Selectivities for the Serotonin Transporter Site.

S. Childers, T. Sexton, C. Thornley, 1996 .

Synthesis of 3 beta-aryl-8-azabicyclo[3.2.1]octanes with high binding affinities and selectivities for the serotonin transporter site.

S. Childers, T. Sexton, C. Thornley, 1996, Journal of medicinal chemistry.

Synthesis of 2β‐Acyl‐3β‐aryl‐8‐azabicyclo(3.2.1)octanes and Their Binding Affinities at Dopamine and Serotonin Transport Sites in Rat Striatum and Frontal Cortex.

S. Childers, T. Sexton, H. Davies, 1994 .

Synthesis of 2 beta-acyl-3 beta-aryl-8-azabicyclo[3.2.1]octanes and their binding affinities at dopamine and serotonin transport sites in rat striatum and frontal cortex.

S. Childers, T. Sexton, H. Davies, 1994, Journal of medicinal chemistry.

Synthesis and SAR development of novel mGluR1 antagonists for the treatment of chronic pain.

W. Greenlee, D. Tulshian, R. Bertorelli, 2012, Bioorganic & medicinal chemistry letters.

2-(2-Furanyl)-7-phenyl[1,2,4]triazolo[1,5-c]pyrimidin-5-amine analogs: highly potent, orally active, adenosine A2A antagonists. Part 1.

D. Tulshian, G. Varty, A. Fawzi, 2005, Bioorganic & medicinal chemistry letters.

Discovery and Structure Enabled Synthesis of 2,6-Diaminopyrimidin-4-one IRAK4 Inhibitors.

D. Tulshian, T. Fischmann, C. Garlisi, 2015, ACS medicinal chemistry letters.

The Discovery and Synthesis of Novel Adenosine Receptor (A2A) Antagonists.

B. Neustadt, Jinsong Hao, D. Tulshian, 2005 .

Absolute configuration of C27H41NO8Si, the diastereoselective product of the rhodium(II) octanoate catalyzed decomposition of a chiral vinyldiazomethane in the presence of 2-acetylpyrrole: A structural study rendered difficult by disorder of a “heavy” atom

D. Churchill, H. Davies, M. Churchill, 1999 .

Cyclopropylcarbene-tungsten complexes + alkynes: a [4 + 2 + 1] cycloaddition route for the construction of seven-membered rings

M. Reid, J. Herndon, J. Harp, 1991 .

Discovery of pyrrolo-benzo-1,4-diazines as potent Na(v)1.7 sodium channel blockers.

D. Tulshian, D. Rindgen, Shu-wei Yang, 2014, Bioorganic & medicinal chemistry letters.

Synthesis and SAR development of novel P2X7 receptor antagonists for the treatment of pain: part 2.

W. Greenlee, D. Tulshian, R. Bertorelli, 2011, Bioorganic & medicinal chemistry letters.

Initial optimization and series evolution of diaminopyrimidine inhibitors of interleukin-1 receptor associated kinase 4.

W. Greenlee, D. Tulshian, Jinhai Yang, 2015, Bioorganic & medicinal chemistry letters.

Synthesis and structure-activity relationships of N-substituted spiropiperidines as nociceptin receptor ligands.

D. Tulshian, A. Fawzi, Hongtao Zhang, 2007, Bioorganic & medicinal chemistry letters.

Synthesis and structure-activity relationships of N-substituted spiropiperidines as nociceptin receptor ligands: part 2.

D. Tulshian, R. Mcleod, A. Fawzi, 2009, Bioorganic & medicinal chemistry letters.

Local cerebral metabolic effects of the novel cocaine analog, WF‐31: Comparisons to fluoxetine

L. Porrino, C. Thornley, Mack D. Miller, 1997, Synapse.