S. Djurić

发表

Compound Collection Enhancement and Paradigms for High-Throughput Screening — an Update

Irini Akritopoulou-Zanze, Philip B. Cox, I. Akritopoulou‐Zanze, 2010 .

Synthesis of Fused Pyrimidinone and Quinolone Derivatives in an Automated High-Temperature and High-Pressure Flow Reactor.

Ying Wang, A. Bogdan, Stevan W Djuric, 2017, The Journal of organic chemistry.

An Integrated Synthesis-Purification System to Accelerate the Generation of Compounds in Pharmaceutical Discovery

Jeffrey Y. Pan, S. Spanton, S. Djurić, 2011 .

LOPHTOR: a convenient flow-based photochemical reactor

A. Vasudevan, J. Trumbull, S. Djurić, 2010 .

Scaffold Oriented Synthesis. Part 1. Design, Preparation, and Biological Evaluation of Thienopyrazoles as Kinase Inhibitors.

J. R. Huth, D. Song, Eric F. Johnson, 2006 .

Applications of MCR-Derived Heterocycles in Drug Discovery

I. Akritopoulou‐Zanze, S. Djurić, 2010 .

Sequential Ugi/Heck cyclization strategies for the facile construction of highly functionalized N-heterocyclic scaffolds

V. Gracias, S. Djurić, J. D. Moore, 2004 .

Synthesis of fused bicyclic imidazoles by sequential van Leusen/ring-closing metathesis reactions.

V. Gracias, S. Djurić, A. Gasiecki, 2005, Organic letters.

Synthesis of fused imidazo azepine derivatives by sequential van Leusen/enyne metathesis reactions

V. Gracias, S. Djurić, A. Gasiecki, 2005 .

Synthesis of fused triazolo-imidazole derivatives by sequential van Leusen/alkyne-azide cycloaddition reactions

V. Gracias, S. Djurić, Daria Darczak, 2005 .

Synthesis of fused imidazole rings by sequential van Leusen/C–H bond activation

V. Gracias, S. Djurić, A. Gasiecki, 2006 .

Synthesis of fused imidazo-pyridine and -azepine derivatives by sequential van Leusen/Heck reactions

X. Beebe, V. Gracias, S. Djurić, 2006 .

Synthesis of novel and uniquely shaped 3-azabicyclo[4.2.0]octan-4-one derivatives by sequential Ugi/[2+2] ene-enone photocycloadditions.

I. Akritopoulou‐Zanze, R. Henry, S. Djurić, 2007, Organic letters.

Concise construction of novel bridged bicyclic lactams by sequenced Ugi/RCM/Heck reactions.

Jeffrey L. Cross, I. Akritopoulou‐Zanze, R. Henry, 2007, Organic letters.

Recent Advances in the Development and Applications of Post-Ugi Transformations

I. Akritopoulou‐Zanze, S. Djurić, 2007 .

Are We There Yet? Applying Thermodynamic and Kinetic Profiling on Embryonic Ectoderm Development (EED) Hit-to-Lead Program.

S. C. Panchal, A. Vasudevan, Chaohong Sun, 2017, Journal of medicinal chemistry.

Synthesis of substituted fused pyridines, pyrazines and pyrimidines by sequential Ugi/inverse electron demand Diels-Alder transformations

I. Akritopoulou‐Zanze, S. Djurić, Ying Wang, 2009 .

Identification of halosalicylamide derivatives as a novel class of allosteric inhibitors of HCV NS5B polymerase.

L. Traphagen, U. Warrior, A. Molla, 2008, Bioorganic & medicinal chemistry letters.

Expedient Diels–Alder cycloadditions with ortho-quinodimethanes in a high temperature/pressure flow reactor

S. Djurić, J. Tsoung, Ying Wang, 2017 .

Synthesis of substituted 3,4 -dihydroquinolin -2 (1H) -one derivatives by sequential Ugi/acrylanilide [6π] -photocyclizations

I. Akritopoulou‐Zanze, R. Henry, S. Djurić, 2007 .

Synthesis of imidazopyridines and purines as potent inhibitors of leukotriene A4 hydrolase.

J. Gierse, J. Miyashiro, T. Penning, 2003, Bioorganic & medicinal chemistry letters.

1,4-Dihydroindeno[1,2-c]pyrazoles with acetylenic side chains as novel and potent multitargeted receptor tyrosine kinase inhibitors with low affinity for the hERG ion channel.

S. Davidsen, G. Gintant, Eric F. Johnson, 2007, Journal of medicinal chemistry.

Rapid analytical characterization of high-throughput chemistry screens utilizing desorption electrospray ionization mass spectrometry

A. Bogdan, N. Talaty, S. Djurić, 2019, Reaction Chemistry & Engineering.

Phorbol ester-induced dermal inflammation in mice: evaluation of inhibitors of 5-lipoxygenase and antagonists of leukotriene B4 receptor.

P. Isakson, S. Yu, S. Djurić, 1994, Journal of lipid mediators and cell signalling.

A post aza Baylis–Hillman/Heck coupling approach towards the synthesis of constrained scaffolds

A. Vasudevan, Pei-San Tseng, S. Djurić, 2006 .

Potent Inhibition of NFAT Activation and T Cell Cytokine Production by Novel Low Molecular Weight Pyrazole Compounds*

Julie A. Wilkins, U. Warrior, Yung-wu Chen, 2001, The Journal of Biological Chemistry.

Eicosanoids and inflammatory bowel disease: regulation and prospects for therapy.

T. Gaginella, S. Djurić, D. Fretland, 1990, Prostaglandins, leukotrienes, and essential fatty acids.

Faculty of 1000 evaluation for Twenty years on: the impact of fragments on drug discovery.

S. Djurić, 2016 .

A versatile synthesis of fused triazolo derivatives by sequential Ugi/alkyne-azide cycloaddition reactions

I. Akritopoulou‐Zanze, V. Gracias, S. Djurić, 2004 .

12(R)- and 12(S)-hydroxyeicosatetraenoic acids: chemistry, biology, and pharmacology.

S. Djurić, D. Fretland, 1989, Prostaglandins, leukotrienes, and essential fatty acids.

SC-41930: an inhibitor of leukotriene B4-stimulated human neutrophil functions.

S. Djurić, R. L. Shone, B. Tsai, 1989, Prostaglandins.

3,5-Bis(trifluoromethyl)pyrazoles: a novel class of NFAT transcription factor regulator.

Xiaoping Zhou, U. Warrior, C. Wegner, 2000, Journal of medicinal chemistry.

Selective C(sp3)−H Aerobic Oxidation Enabled by Decatungstate Photocatalysis in Flow

T. Noël, M. Fagnoni, S. Djurić, 2018, Angewandte Chemie.

A Dominant-negative p38 MAPK Mutant and Novel Selective Inhibitors of p38 MAPK Reduce Insulin-stimulated Glucose Uptake in 3T3-L1 Adipocytes without Affecting GLUT4 Translocation*

R. Somwar, A. Klip, C. Rondinone, 2002, The Journal of Biological Chemistry.

Inhibition of p56lckTyrosine Kinase by Isothiazolones

U. Warrior, Yung-wu Chen, P. Wiedeman, 1999 .

Therapeutic regulation of inflammation and angiogenesis in cancer, arthritis, and asthma, sixth annual midwest meeting, Chicago, IL, USA, March 16, 1998

K. Glaser, S. Djurić, J. Winkler, 1999, Inflammation Research.

Cloning and characterization of the glucagon receptor from cynomologous monkey

T. Pederson, C. Collins, R. Reilly, 2004, Peptides.

Glucagon receptor antagonists for the treatment of type II diabetes: current prospects.

S. Djurić, C. W. Lin, N. Grihalde, 2002, Current opinion in investigational drugs.

Antiinflammatory effects of second-generation leukotriene B4 receptor antagonist, SC-53228: Impact upon Leukotriene B4- and 12(R)-HETE- mediated events

P. Isakson, T. Penning, S. Docter, 1995, Inflammation.

Leukotriene B4-induced granulocyte trafficking in guinea pig dermis

T. Penning, S. Yu, S. Djurić, 1993, Inflammation.

Medicinal chemist

S. Djurić, 2006 .

Quaternary substituted PDE4 inhibitors I: the synthesis and in vitro evaluation of a novel series of oxindoles.

C. Hulme, S. Djurić, G. Poli, 1998, Bioorganic & medicinal chemistry letters.

Electrochemical Aminoxyl-Mediated α-Cyanation of Secondary Piperidines for Pharmaceutical Building Block Diversification.

S. Stahl, S. Djurić, A. Lennox, 2018, Journal of the American Chemical Society.

Orally active indole N-oxide PDE4 inhibitors.

C. Hulme, R. Labaudinière, S. Djurić, 1998, Bioorganic & medicinal chemistry letters.

2-Substituted-4-methoxybenzimidazole-based PDE4 inhibitors.

J. Regan, S. Djurić, B. Hanney, 1998, Bioorganic & medicinal chemistry letters.

Discovery of 2-[4-{{2-(2S,5R)-2-cyano-5-ethynyl-1-pyrrolidinyl]-2-oxoethyl]amino]- 4-methyl-1-piperidinyl]-4-pyridinecarboxylic acid (ABT-279): a very potent, selective, effective, and well-tolerated inhibitor of dipeptidyl peptidase-IV, useful for the treatment of diabetes.

K. Longenecker, J. Segreti, H. Sham, 2006, Journal of medicinal chemistry.

TH1 and TH2 cytokine inhibition by 3,5-bis(trifluoromethyl)pyrazoles, a novel class of immunomodulators.

Julie A. Wilkins, U. Warrior, M. Nakane, 2002, Cellular immunology.

Preliminary in vivo pharmacokinetic and pharmacodynamic evaluation of a novel calcineurin-independent inhibitor of NFAT

U. Christians, R. Morris, W. Jacobsen, 2004, Transplant international : official journal of the European Society for Organ Transplantation.

Benzofuran based PDE4 inhibitors.

C. Hulme, J. Regan, S. Djurić, 1999, Bioorganic & medicinal chemistry.

High‐Throughput Reaction Screening with Nanomoles of Solid Reagents Coated on Glass Beads

A. Dombrowski, A. Vasudevan, Ying Wang, 2019, Angewandte Chemie.

Preliminary in vivo pharmacokinetic and pharmacodynamic evaluation of a novel calcineurin‐independent inhibitor of NFAT

U. Christians, R. Morris, W. Jacobsen, 2004 .

A simple and efficient automatable one step synthesis of triazolopyridines from carboxylic acids

D. Sauer, S. Djurić, Kathy A Sarris, 2007 .

A simple and efficient one step synthesis of benzoxazoles and benzimidazoles from carboxylic acids

D. Sauer, S. Djurić, Kathy A Sarris, 2006 .

De Novo Design, Synthesis, and Biological Evaluation of 3,4-Disubstituted Pyrrolidine Sulfonamides as Potent and Selective Glycine Transporter 1 Competitive Inhibitors.

Justin D Dietrich, A. Vasudevan, J. Sydor, 2018, Journal of medicinal chemistry.

Quaternary substituted PDE IV inhibitors II: the synthesis and in vitro evaluation of a novel series of gamma-lactams.

J. Mason, C. Hulme, R. Labaudinière, 1998, Bioorganic & medicinal chemistry letters.

Kelatorphan and related analogs: potent and selective inhibitors of leukotriene A4 hydrolase

T. Penning, S. Djurić, G. Krivi, 1995 .

A High-Capacity Scintillation Proximity Assay for the Discovery and Evaluation of ZAP-70 Tandem SH2 Domain Antagonists

U. Warrior, H. Yoon, J. Trevillyan, 1998 .

Inflammation of guinea pig dermis

T. Gaginella, S. Djurić, D. Widomski, 1990, Inflammation.

Effect of a leukotriene B4 receptor antagonist on leukotriene B4-induced neutrophil chemotaxis in cavine dermis

S. Djurić, D. Widomski, R. L. Shone, 1989, Inflammation.

Optical isomers of a leukotriene B4 antagonist have differential effects on granulocyte diapedesis in the guinea pig dermis.

S. Yu, S. Djurić, D. Widomski, 1992, Chirality.

Enantioselective total synthesis and pharmacologic profile of 12-deoxy-12(S)-methyl leukotriene B4

J. Miyashiro, T. Penning, S. Djurić, 1991 .

Structure−Activity Relationship Studies on 1-[2-(4-Phenylphenoxy)ethyl]pyrrolidine (SC-22716), a Potent Inhibitor of Leukotriene A4 (LTA4) Hydrolase

J. Gierse, J. Miyashiro, T. Penning, 2000 .

Synthesis and pharmacological activity of rationally designed inhibitors of the leukotriene A4 hydrolase enzyme

T. Penning, R. M. Huff, S. Djurić, 1992 .

Improved Procedure for the Reduction of N-Acyloxazolidinones

J. Miyashiro, T. Penning, V. Kalish, 1990 .

Synthesis of therapeutically useful prostaglandin and prostacyclin analogs

P. Collins, S. Djurić, 1993 .

Synthesis of diazepinones via intramolecular transamidation.

A. Vasudevan, S. Djurić, C. I. Villamil, 2004, Organic letters.

7-[3-(4-acetyl-3-methoxy-2-propylphenoxy)propoxy]-3,4-dihydro-8- propyl-2H-1-benzopyran-2-carboxylic acid: an orally active selective leukotriene B4 receptor antagonist.

G. Butchko, P. Collins, S. Djurić, 1989, Journal of medicinal chemistry.

Scaffold oriented synthesis. Part 4: design, synthesis and biological evaluation of novel 5-substituted indazoles as potent and selective kinase inhibitors employing heterocycle forming and multicomponent reactions.

Eric F. Johnson, I. Akritopoulou‐Zanze, P. Kovar, 2011, Bioorganic & medicinal chemistry letters.

Palladium(0) catalyzed coupling oftrans-1,2-Bis(tri-n-butylstannyl)ethylene with aromatic halides: a convenient Synthesis of substitutedtrans-β-bromostyrenes

T. Penning, S. Djurić, R. A. Haack, 1988 .

Synthesis and antibacterial activity of 6-O-arylpropargyl-9-oxime-11,12-carbamate ketolides.

M. Mitten, X. Beebe, S. Djurić, 2004, Bioorganic & medicinal chemistry letters.

Synthesis of Substituted Fused Pyridines, Pyrazines and Pyrimidines by Sequential Ugi/Inverse Electron Demand Diels—Alder Transformations.

I. Akritopoulou‐Zanze, S. Djurić, Ying Wang, 2010 .

Synthesis of Novel and Uniquely Shaped 3‐Azabicyclo[4.2.0]octan‐4‐one Derivatives by Sequential Ugi/[2 + 2] Ene—Enone Photocycloadditions.

I. Akritopoulou‐Zanze, R. Henry, S. Djurić, 2007 .

A Versatile Synthesis of Fused Triazolo Derivatives by Sequential Ugi/Alkyne—Azide Cycloaddition Reactions.

I. Akritopoulou‐Zanze, V. Gracias, S. Djurić, 2005 .

Synthesis of novel fused isoxazoles and isoxazolines by sequential Ugi/INOC reactions

I. Akritopoulou‐Zanze, V. Gracias, S. Djurić, 2004 .

Pd-PEPPSI-IPent-SiO2 : A Supported Catalyst for Challenging Negishi Coupling Reactions in Flow.

A. Bogdan, S. Djurić, M. Organ, 2017, Angewandte Chemie.

Efficient Pd-catalyzed synthesis of 2-arylaminopyrimidines via microwave irradiation

A. Vasudevan, Henry Q. Zhang, S. Djurić, 2006 .

Silicon in synthesis: an exceptionally short synthesis of dl-11.alpha.-hydroxyestrone methyl ether

T. Sarkar, S. Djurić, P. Magnus, 1980 .

Rapid and efficient synthesis of 1,2,4-oxadiazoles utilizing polymer-supported reagents under microwave heating.

D. Sauer, S. Djurić, Ying Wang, 2005, Organic letters.

Synthesis of Fused Triazolo‐Imidazole Derivatives by Sequential van Leusen/Alkyne—Azide Cycloaddition Reactions.

V. Gracias, S. Djurić, Daria Darczak, 2006 .

Recent Advances in the Development and Applications of Post-Ugi Transformations

I. Akritopoulou‐Zanze, S. Djurić, 2007 .

A simple and efficient one step synthesis of 1,3,4-oxadiazoles utilizing polymer-supported reagents and microwave heating

D. Sauer, S. Djurić, Ying Wang, 2006 .

A mild and convenient procedure for the N-formylation of secondary amines using organosilicon chemistry

S. Djurić, 1984 .

An expeditious and convenient synthesis of acylsulfonamides utilizing polymer-supported reagents

D. Sauer, S. Djurić, Kathy A Sarris, 2007 .

Enabling Chemistry Technologies and Parallel Synthesis-Accelerators of Drug Discovery Programmes.

A. Bogdan, A. Vasudevan, Ying Wang, 2017, Progress in medicinal chemistry.

48 – Organosilicon Compounds in Organic Synthesis

T. Sarkar, S. Djurić, P. Magnus, 1982 .

Continuous flow Negishi cross-couplings employing silica-supported Pd-PEPPSI–IPr precatalyst

Ana L. Aguirre, A. Bogdan, S. Djurić, 2016 .

High-Temperature Boc Deprotection in Flow and Its Application in Multistep Reaction Sequences.

A. Bogdan, A. Dombrowski, S. Djurić, 2016, Organic letters.

Current status and future prospects for enabling chemistry technology in the drug discovery process

Charles W. Hutchins, C. Hutchins, N. Talaty, 2016, F1000Research.

Ultrasound-assisted click chemistry in continuous flow

S. Djurić, J. Hochlowski, N. Tu, 2011, Molecular Diversity.

Small Molecule Library Synthesis Using Segmented Flow

Jeffrey L. Cross, I. Akritopoulou‐Zanze, S. Djurić, 2011, Molecules.

Synthesis of fused bicyclic imidazoles by sequential van Leusen/ring-closing metathesis reactions.

V. Gracias, S. Djurić, A. Gasiecki, 2005, Organic letters.

Photochemical Flow Synthesis of 3‐Hydroxyazetidines

A. Dombrowski, I. Baxendale, S. Djurić, 2019, ChemPhotoChem.

An Expeditious and Convenient Synthesis of Acylsulfonamides Utilizing Polymer‐Supported Reagents.

D. Sauer, S. Djurić, Kathy A Sarris, 2007 .

Silicon in synthesis: stabase adducts - a new primary amine protecting group: alkylation of ethyl glycinate

S. Djurić, P. Magnus, J. J. Venit, 1981 .

Synthesis of a novel prostacyclin analog containing the bicyclo[3.1.0] hexane ring system. Application of molecular mechanics calculations to organic synthesis

J. Snyder, S. Djurić, M. Miyano, 1986 .

Continuous-Flow Microfluidic Electrochemical Synthesis: Investigating a New Tool for Oxidative Chemistry

D. Sauer, G. Roth, R. Stalder, 2013, Journal of Flow Chemistry.

Automated library synthesis of cyclopropyl boronic esters employing diazomethane in a tube-in-tube flow reactor.

Jeffrey Y. Pan, Ying Wang, Jeffrey Y Pan, 2016, Organic & biomolecular chemistry.

Scaffold oriented synthesis. Part 2: Design, synthesis and biological evaluation of pyrimido-diazepines as receptor tyrosine kinase inhibitors.

Zhiqin Ji, Irini Akritopoulou-Zanze, K. Glaser, 2008, Bioorganic & medicinal chemistry letters.

A facile and practical one-pot ‘catch and release’ synthesis of substituted guanidines

D. Sauer, S. Djurić, Ying Wang, 2009 .

Synthesis of 5-fluoroprostacyclin

S. Djurić, R. Pappo, R. B. Garland, 1987 .

An expedient route to diaza-spirocycles utilizing a sequential multicomponent α-aminoallylation/ring-closing metathesis strategy

I. Akritopoulou‐Zanze, V. Gracias, S. Djurić, 2006 .

An Expedient Route to Diaza-Spirocycles Utilizing a Sequential Multicomponent α-Aminoallylation/Ring-Closing Metathesis Strategy.

I. Akritopoulou‐Zanze, V. Gracias, S. Djurić, 2007 .

A rearrangement of 3-hydroxyazetidines into 2-oxazolines.

A. Dombrowski, I. Baxendale, S. Djurić, 2020, The Journal of organic chemistry.

Chapter 18. Recent Advances in the Treatment of Inflammatory Bowel Disease

T. Gaginella, S. Djurić, D. Fretland, 1989 .

Development of a p38 Kinase Binding Assay for High Throughput Screening

R. Simmer, U. Warrior, D. Burns, 1999, Journal of biomolecular screening.

Palladium(0) Catalyzed Coupling of trans‐1,2‐Bis(tri‐n‐butylstannyl)ethylene with Aromatic Halides: A Convenient Synthesis of Substituted trans‐β‐Bromostyrenes.

T. Penning, S. Djurić, R. A. Haack, 1988 .

Faculty Opinions recommendation of PhotoAffinity Bits: A Photoaffinity-Based Fragment Screening Platform for Efficient Identification of Protein Ligands.

S. Djurić, 2020 .

T cell activation induces a noncoding RNA transcript sensitive to inhibition by immunosuppressant drugs and encoded by the proto-oncogene, BIC.

D. Halbert, D. Haasch, Yung-wu Chen, 2002, Cellular immunology.

High-Throughput Reaction Screening with Nanomoles of Solid Reagents Coated on Glass Beads.

Noah P Tu, Anil Vasudevan, A. Dombrowski, 2019, Angewandte Chemie.

Hit to Lead optimization of a novel class of squarate-containing polo-like kinases inhibitors.

A. Vasudevan, Eric F. Johnson, V. Giranda, 2012, Bioorganic & medicinal chemistry letters.

The synthesis and biological evaluation of a novel series of antimicrobials of the oxazolidinone class.

R. Ulrich, P. Wiedeman, K. Marsh, 2002, Bioorganic & medicinal chemistry letters.

Synthesis of N-arylated oxazolidinones via a palladium catalyzed cross coupling reaction. Application to the synthesis of the antibacterial agent Dup-721

P. Wiedeman, S. Djurić, Marina A. Pliushchev, 2001 .

Design, synthesis and structure-activity relationships of 6-O-arylpropargyl diazalides with potent activity against multidrug-resistant Streptococcus pneumoniae.

N. Soni, R. Clark, K. Marsh, 2005, Bioorganic & Medicinal Chemistry Letters.

Synthesis and antibacterial activity of novel bifunctional macrolides.

I. Akritopoulou‐Zanze, S. Djurić, G. Stone, 2004, Bioorganic & medicinal chemistry letters.

The stereoselective synthesis of novel macrolide antibacterial agents via an intramolecular 1,3-dipolar cycloaddition of azomethine ylide

R. Clark, S. Djurić, Xiaoling Zhang, 2004 .

Design, Synthesis and Structure—Activity Relationships of 6-O-Arylpropargyl Diazalides with Potent Activity Against Multidrug-Resistant Streptococcus Pneumoniae.

N. Soni, R. Clark, K. Marsh, 2005 .

Novel 12-membered ring macrolides with activity against erythromycin-resistant organisms.

S. Djurić, Xiaoling Zhang, Zhenkun Ma, 2003, The Journal of antibiotics.

The Stereoselective Synthesis of Novel Macrolide Antibacterial Agents via an Intramolecular 1,3-Dipolar Cycloaddition of Azomethine Ylide.

R. Clark, S. Djurić, Xiaoling Zhang, 2004 .

Novel 12‐Membered Ring Macrolides with Activity Against Erythromycin‐Resistant Organisms.

S. Djurić, Xiaoling Zhang, Zhenkun Ma, 2003 .

1,4-Dihydroindeno[1,2-c]pyrazoles as novel multitargeted receptor tyrosine kinase inhibitors.

S. Davidsen, I. Akritopoulou‐Zanze, M. Michaelides, 2006, Bioorganic & Medicinal Chemistry Letters.

The synthesis and biological evaluation of a novel series of indole PDE4 inhibitors I.

C. Hulme, R. Labaudinière, S. Djurić, 1998, Bioorganic & medicinal chemistry letters.

Novel cytokine release inhibitors. Part IV: analogs of podocarpic acid.

A. Zilberstein, J. Regan, S. Djurić, 1999, Bioorganic & medicinal chemistry letters.

Accelerated multi-reagent copper catalysed coupling reactions in micro droplets and thin films

R. Cooks, A. Bogdan, N. Talaty, 2018 .

SC-41930 inhibits neutrophil infiltration of the cavine dermis induced by 12(R)-hydroxyeicosatetraenoic acid.

J. Miyashiro, T. Penning, S. Djurić, 1989, Prostaglandins, leukotrienes, and essential fatty acids.

12(R)-hydroxyeicosatetraenoic acid is a neutrophil chemoattractant in the cavine, lapine, murine and canine dermis.

J. Miyashiro, T. Penning, S. Djurić, 1989, Prostaglandins, leukotrienes, and essential fatty acids.

Faculty Opinions recommendation of Organic chemistry. Nanomole-scale high-throughput chemistry for the synthesis of complex molecules.

Jasmina Marjanovic, Stevan Djuric, J. Marjanovic, 2015 .

Zotarolimus, a Novel Sirolimus Analogue With Potent Anti-proliferative Activity on Coronary Smooth Muscle Cells and Reduced Potential for Systemic Immunosuppression

Yung-wu Chen, J. Trevillyan, G. Carter, 2007, Journal of cardiovascular pharmacology.

An Automated Synthesis–Purification–Sample-Management Platform for the Accelerated Generation of Pharmaceutical Candidates

Jeffrey Y. Pan, Noah P Tu, Philip A Searle, 2014, Journal of laboratory automation.

Second-generation leukotriene B4 receptor antagonists related to SC-41930: heterocyclic replacement of the methyl ketone pharmacophore.

J. Snyder, J. Miyashiro, T. Penning, 1995, Journal of Medicinal Chemistry.

Synthesis and pharmacological activity of SC-53228, a leukotriene B4 receptor antagonist with high intrinsic potency and selectivity

T. Rao, S. Docter, T. Gaginella, 1994 .

Inhibition of p56(lck) tyrosine kinase by isothiazolones.

U. Warrior, P. Wiedeman, J. Trevillyan, 1999, Archives of biochemistry and biophysics.

Chemoselective reductions of 2-acyl-1H-indole-3-carboxaldehydes

S. Djurić, R. Herbert, F. G. Holliman, 1985 .

RNA: Opening New Doors in Medicinal Chemistry.

Stevan W Djuric, Amanda L Garner, S. Djurić, 2020, ACS medicinal chemistry letters.

Tandem Click-Suzuki reactions in a novel flow reactor incorporating immobilized and exchangeable reagents

S. Djurić, Kathy A Sarris, N. Tu, 2015 .

Ultrasound-assisted click chemistry in continuous flow

S. Djurić, J. Hochlowski, N. Tu, 2012, Molecular diversity.

Nucleophilic aromatic substitution of heterocycles using a high-temperature and high-pressure flow reactor

A. Bogdan, S. Djurić, Ying Wang, 2016 .

Integrated Platform for Expedited Synthesis-Purification-Testing of Small Molecule Libraries.

Aleksandra Baranczak, Jasmina Marjanovic, Noah P Tu, 2017, ACS medicinal chemistry letters.

Scaffold oriented synthesis. Part 1: Design, preparation, and biological evaluation of thienopyrazoles as kinase inhibitors.

J. R. Huth, D. Song, Eric F. Johnson, 2006, Bioorganic & medicinal chemistry letters.

Novel cyclic compounds as potent phosphodiesterase 4 inhibitors.

J. Mason, S. Djurić, B. Hanney, 1998, Journal of medicinal chemistry.

Rapamycin analogs with reduced systemic exposure.

P. Wiedeman, J. Trevillyan, G. Carter, 2005, Bioorganic & medicinal chemistry letters.

Topography-biased compound library design: the shape of things to come?

Irini Akritopoulou-Zanze, J. T. Metz, I. Akritopoulou‐Zanze, 2007, Drug discovery today.

Selective C(sp3)−H Aerobic Oxidation Enabled by Decatungstate Photocatalysis in Flow

T. Noël, Davide Ravelli, M. Fagnoni, 2018, Angewandte Chemie.

Putting Thought to Paper: A μARCS Protease Screen

U. Warrior, D. Burns, D. Groebe, 2003 .

Electrochemical Aminoxyl-Mediated α-Cyanation of Secondary Piperidines for Pharmaceutical Building Block Diversification.

S. Stahl, S. Djurić, A. Lennox, 2018, Journal of the American Chemical Society.

Contribution of indazolinone tautomers to kinase activity.

A. Vasudevan, C. Abad-Zapatero, K. Stewart, 2012, Bioorganic & medicinal chemistry letters.

Effect of the leukotriene B4 receptor antagonist SC-41930 on colonic inflammation in rat, guinea pig and rabbit.

T. Gaginella, S. Djurić, D. Widomski, 1990, The Journal of pharmacology and experimental therapeutics.