J. McNulty

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A Pronounced Anionic Effect in the Pd‐Catalyzed Buchwald–Hartwig Amination Reaction Revealed in Phosphonium Salt Ionic Liquids

T. Bender, J. McNulty, Sreedhar Cheekoori, 2007 .

Enol ethers as carbonyl surrogates in a modification of the Povarov synthesis of 3-aryl quinolines and their anti-Toxoplasma activity.

R. Yolken, J. McNulty, L. Jones-Brando, 2016, Organic & biomolecular chemistry.

Synthesis and anti-toxoplasmosis activity of 4-arylquinoline-2-carboxylate derivatives.

R. Yolken, J. McNulty, L. Jones-Brando, 2014, Organic & biomolecular chemistry.

Induction of Apoptotic Cell Death Specifically in Rat and Human Cancer Cells by Pancratistatin

J. McNulty, S. Pandey, N. Kekre, 2005, Artificial cells, blood substitutes, and immobilization biotechnology.

Removal and Recovery of Phenols from Industrial Waste Effluents with Amberlite XAD Polymeric Adsorbents

J. McNulty, E. H. Crook, R. McDonnell, 1975 .

A novel synthetic C-1 analogue of 7-deoxypancratistatin induces apoptosis in p53 positive and negative human colorectal cancer cells by targeting the mitochondria: enhancement of activity by tamoxifen

T. Hudlický, J. McNulty, S. Pandey, 2012, Investigational New Drugs.

Structure-activity studies on acetylcholinesterase inhibition in the lycorine series of Amaryllidaceae alkaloids.

J. Brennan, J. McNulty, J. Little, 2010, Bioorganic & medicinal chemistry letters.

Discovery of potent antiviral (HSV-1) quinazolinones and initial structure-activity relationship studies.

P. Piazza, V. Nimgaonkar, L. McClain, 2017, Bioorganic & medicinal chemistry letters.

Microwave-assisted, aqueous wittig reactions: organic-solvent- and protecting-group-free chemoselective synthesis of functionalized alkenes.

J. McNulty, P. Das, David C. McLeod, 2010, Chemistry.

A short synthesis of the anti-leukemic sesquiterpene (+)-caparratriene employing aqueous Wittig chemistry

J. McNulty, P. Das, 2010 .

Highly Stereoselective and General Synthesis of (E)-Stilbenes and Alkenes by Means of an Aqueous Wittig Reaction

J. McNulty, P. Das, 2009 .

Aqueous Wittig reactions of semi-stabilized ylides. A straightforward synthesis of 1,3-dienes and 1,3,5-trienes

J. McNulty, P. Das, 2009 .

Discovery of a Robust and Efficient Homogeneous Silver(I) Catalyst for the Cycloaddition of Azides onto Terminal Alkynes

J. McNulty, K. Keskar, Kunal Keskar, 2012 .

Synthesizing Novel Anthraquinone Natural Product-Like Compounds to Investigate Protein-Ligand Interactions in Both an in Vitro and in Vivo Assay: An Integrated Research-Based Third-Year Chemical Biology Laboratory Course.

J. McNulty, N. McKenzie, Meghan J McFadden, 2012 .

Isolation of flavonoids from the heartwood and resin of Prunus avium and some preliminary biological investigations.

D. Crankshaw, Gerard D. Wright, L. Ejim, 2009, Phytochemistry.

Sensitization of human melanoma cells by tamoxifen to apoptosis induction by pancratistatin, a nongenotoxic natural compound

J. McNulty, S. Chatterjee, S. Pandey, 2011, Melanoma research.

Structurally simplified biphenyl combretastatin A4 derivatives retain in vitro anti-cancer activity dependent on mitotic arrest

J. McNulty, S. Pandey, S. van den Berg, 2017, PloS one.

R430: A potent inhibitor of DNA and RNA viruses

R. Yolken, R. Ptak, A. Chattopadhyay, 2018, Scientific Reports.

Total Synthesis of the Natural Product (+)-trans-Dihydronarciclasine via an Asymmetric Organocatalytic [3+3]-Cycloaddition and discovery of its potent anti-Zika Virus (ZIKV) Activity

R. Yolken, J. McNulty, C. Zepeda-Velázquez, 2016 .

Potent and selective inhibition of human cytochrome P450 3A4 by seco-pancratistatin structural analogs.

D. Crankshaw, Mohini Singh, J. McNulty, 2010, Bioorganic & medicinal chemistry letters.

Structure-activity studies on seco-pancratistatin analogs: potent inhibitors of human cytochrome P450 3A4.

D. Crankshaw, Mohini Singh, J. McNulty, 2009, Bioorganic & medicinal chemistry letters.

Selective cytochrome P450 3A4 inhibitory activity of Amaryllidaceae alkaloids.

D. Crankshaw, Mohini Singh, J. McNulty, 2009, Bioorganic & medicinal chemistry letters.

Scope and mechanistic insights into the use of tetradecyl(trihexyl)phosphonium bistriflimide: a remarkably selective ionic liquid solvent for substitution reactions.

A. Robertson, J. McNulty, Sreedhar Cheekoori, 2006, Chemistry.

A mild esterification process in phosphonium salt ionic liquid

A. Robertson, J. McNulty, Sreedhar Cheekoori, 2005 .

Dichotomous Reactivity in the Reaction of Triethyl‐ and Triphenylphosphane HBr Salts with Dimethyl Acetals: A Novel Entry to α‐Alkoxy‐Functionalized Ylides and General Synthesis of Vinyl Ethers and Alkoxy Dienes

J. McNulty, P. Das, 2010 .

Suzuki cross-coupling reactions of aryl halides in phosphonium salt ionic liquid under mild conditions.

James McNulty, Alfredo Capretta, A. Robertson, 2002, Chemical communications.

One step entry to P,O- and P,N-type heterocyclic tertiary phosphine ligands and application in Suzuki-Miyaura cross-coupling reactions.

A. Robertson, J. McNulty, C. Kennedy, 2011, Organic & biomolecular chemistry.

Efficient palladium-catalysed carbonylative and Suzuki–Miyaura cross-coupling reactions with bis(di-tert-butylphosphino)-o-xylene

M. Sliwinski, A. Robertson, J. McNulty, 2009 .

A synthesis of sulfonamide analogs of platensimycin employing a palladium-mediated carbonylation strategy

J. McNulty, A. Capretta, J. Nair, 2009 .

Novel class of tertiary phosphine ligands based on a phospha-adamantane framework and use in the Suzuki cross-coupling reactions of aryl halides under mild conditions.

A. Robertson, J. McNulty, A. Capretta, 2003, Organic letters.

The first well-defined silver(I)-complex-catalyzed cycloaddition of azides onto terminal alkynes at room temperature.

J. McNulty, Ramesh Vemula, K. Keskar, 2011, Chemistry.

Mild Chemical and Biological Synthesis of Donor–Acceptor Flanked Reporter Stilbenes: Demonstration of a Physiological Wittig Olefination Reaction

J. McNulty, David C. McLeod, 2012 .

P‐Phenyl‐2,2,6,6‐tetramethylphosphorinan‐4‐ol: An Air‐Stable P,O‐Type Ligand for Palladium‐Mediated Cross‐Coupling Reactions

A. Robertson, J. McNulty, Ehsan Ullah, 2010 .

A novel P,O-type phosphorinane ligand for the Suzuki–Miyaura cross-coupling of aryl chlorides

A. Robertson, J. McNulty, Ehsan Ullah, 2009 .

Phthalide: a direct building-block towards P,O and P,N hemilabile ligands. Application in the palladium-catalysed Suzuki-Miyaura cross-coupling of aryl chlorides.

J. McNulty, K. Keskar, 2013, Organic & biomolecular chemistry.

Solid-phase Suzuki cross-coupling reactions using a phosphine ligand based on a phospha-adamantane framework

Stephan A. Ohnmacht, K. Bleicher, J. McNulty, 2004 .

Antimitotic activity of structurally simplified biaryl analogs of the anticancer agents colchicine and combretastatin A4.

S. Joshi, J. McNulty, S. van den Berg, 2015, Bioorganic & Medicinal Chemistry Letters.

Cytochrome P450 3A4 Inhibitory Activity Studies within the Lycorine series of Alkaloids

D. Crankshaw, Mohini Singh, J. McNulty, 2010, Natural product communications.

Cancer Cell International CANCER CELL INTERNATIONAL

J. McNulty, S. Pandey, J. Nair, 2007 .

Antineoplastic agents. 380. Isolation and X-ray crystal structure determination of isoaaptamine from the Republic of Singapore Hymeniacidon sp. and conversion to the phosphate prodrug hystatin 1.

Michael D. Williams, R. Pettit, H. Hoffmann, 2004, Journal of natural products.

Phospha-adamantanes as ligands for organopalladium chemistry: aminations of aryl halides

J. McNulty, A. Capretta, Timothy J. Brenstrum, 2004 .

Wittig Reactions of Trialkylphosphine-derived Ylides: New Directions and Applications in Organic Synthesis

J. McNulty, C. Zepeda-Velázquez, P. Das, 2015 .

A convergent synthesis of the immunosuppressant FTY720 employing aqueous Wittig chemistry

J. McNulty, Janice Calzavara, 2011 .

Tandem oxidative radical fragmentation–rearrangement of 2-amino-1,3-benzylidene acetals: a short entry to densely functionalised fully differentiated oxazolidinones

J. McNulty, Janice Calzavara, 2013 .

A concise enantioselective synthesis of N-morpholinosphingosines from D-aspartic acid

Zhi-Hui Lu, J. McNulty, C. W. Jefford, 1995 .

The ultrasound promoted Knoevenagel condensation of aromatic aldehydes

J. McNulty, J. Steere, S. Wolf, 1998 .

One-step synthesis of reusable, polymer-supported tri-alkyl phosphine ligands. Application in Suzuki–Miyaura and alkoxycarbonylation reactions

M. Sliwinski, A. Robertson, J. McNulty, 2012 .

A Tandem “On-Palladium” Heck–Jeffery Amination Route Toward the Synthesis of Functionalized Indole-2-carboxylates

J. McNulty, K. Keskar, 2011 .

DualPhos: a versatile, chemoselective reagent for two-carbon aldehyde to latent (E)-alkenal homologation and application in the total synthesis of phomolide G

J. McNulty, David C. McLeod, 2016, Royal Society Open Science.

Highly Chemoselective Mono‐Suzuki Arylation Reactions on All Three Dichlorobenzene Isomers and Applications Development

A. Robertson, J. McNulty, Ehsan Ullah, 2012 .

Formamidine as a Versatile Protecting Group for Primary Amines: A Mild Procedure for Hydrolytic Removal

J. McNulty, I. V. Still, D. Toste, 1994 .

One-pot, multicomponent synthesis of 2,3-disubstituted quinazolin-ones with potent and selective activity against Toxoplasma gondii.

R. Yolken, J. McNulty, L. Jones-Brando, 2018, Bioorganic & medicinal chemistry letters.

A highly efficient general synthesis of phosphine–borane complexes

J. McNulty, Yuehui Zhou, 2004 .

Antineoplastic agents 491. Synthetic conversion of aaptamine to isoaaptamine, 9-demethylaaptamine, and 4-methylaaptamine.

P. Blumberg, R. Pettit, N. Lewin, 2004, The Journal of organic chemistry.

Stereoselective Wittig olefination reactions employing a novel ortho-P-aryl alkoxide effect

J. McNulty, K. Keskar, 2008 .

An improved synthesis of α-phosphonoenamines based on a modified Peterson olefination

J. McNulty, P. Das, D. Gosciniak, 2008 .

Phosphonium Salt Catalyzed Henry Nitroaldol Reactions

A. Robertson, J. McNulty, A. Capretta, 2004 .

Development of a robust reagent for the two-carbon homologation of aldehydes to (E)-α,β-unsaturated aldehydes in water

J. McNulty, C. Zepeda-Velázquez, David C. McLeod, 2013 .

Formamidine as a Versatile Protecting Group for Primary Amines: A Mild Prodedure for Hydrolytic Removal.

J. McNulty, I. V. Still, D. Toste, 1994 .

Diastereoselective pictet-spengler reactions of L-(boc)prolinal: a biomimetic synthesis of eudistomins H and I, and woodinine

J. McNulty, I. V. Still, 1991 .

A Robust, Well-Defined Homogeneous Silver(I) Catalyst for Mild Intramolecular Hydroamination of 2-Ethynylanilines Leading to Indoles

J. McNulty, K. Keskar, 2014 .

A direct synthesis of functionalized styrenes and terminal 1,3-dienes via aqueous Wittig chemistry with formalin

J. McNulty, P. Das, David C. McLeod, 2011 .

Selective addition of Grignard reagents to 2,3-O-isopropylidene bis-Weinreb tartaric acid amide

J. McNulty, Veronika Grunner, J. Mao, 2001 .

The Enantioselective Synthesis of β‐Amino Acids, their α‐hydroxy derivatives, and the N‐terminal components of bestatin and microginin

Jian Bo Wang, Zhi-Hui Lu, J. McNulty, 1996 .

The phosphate–carboxylate mixed-anhydride method: a mild, efficient process for ester and amide bond construction

A. Robertson, J. McNulty, Ramesh Vemula, 2012 .

The Ultrasound-Promoted Knoevenagel Condensation of Aromatic Aldehydes.

J. McNulty, J. Steere, S. Wolf, 2010 .

Antineoplastic agents. 362. Isolation and X-ray crystal structure of dibromophakellstatin from the Indian ocean sponge Phakellia mauritiana.

M. Boyd, D. L. Herald, J. McNulty, 1997, Journal of natural products.

Synthesis of non-nucleoside anti-viral cyclopropylcarboxacyl hydrazones and initial anti-HSV-1 structure-activity relationship studies.

P. Piazza, V. Nimgaonkar, L. McClain, 2020, Bioorganic & medicinal chemistry letters.

Unusual Magnesium Chloride Catalyzed Non‐Evans anti‐Aldol Reactions of an Enolizable L‐Threose Derivative

M. Sliwinski, J. McNulty, S. Pandey, 2007 .

A synthesis of 3-deoxydihydrolycoricidine: refinement of a structurally minimum pancratistatin pharmacophore.

J. McNulty, S. Pandey, V. Larichev, 2005, Bioorganic & medicinal chemistry letters.

Selective methylation and stereoselective reduction of a β-carboline to a N(2)-methyl-1,2,3,4-tetrahydro-β-carboline.

J. McNulty, I. V. Still, 1995 .

The Synthesis of Eudistomins S and T: b-carbolines from the Tunicate Eudistoma olivaceum

J. McNulty, I. V. Still, 1989 .

Selective apoptosis-inducing activity of crinum-type Amaryllidaceae alkaloids.

C. Codina, J. McNulty, S. Pandey, 2007, Phytochemistry.

Efficient carbonylation reactions in phosphonium salt ionic liquids: anionic effects.

A. Robertson, J. McNulty, J. Nair, 2007, Organic letters.

The synthesis of densely functionalised α-acyloxy enaminals and enaminones via a novel homogeneous silver(i) catalysed rearrangement.

J. McNulty, C. Zepeda-Velázquez, Chanti Babu Dokuburra, 2019, Chemical communications.

Novel chiral phosphines derived from limonene: the synthesis and structure of 4,8-dimethyl-2-phosphabicyclo[3.3.1]nonane

A. Robertson, J. McNulty, Christine J. Bradaric, 2001 .

Phosphorinanes as ligands for palladium-catalyzed cross-coupling chemistry.

S. Zavorine, J. Britten, A. Robertson, 2006, Organic letters.

Asymmetric Organocatalytic Stepwise [2+2] Entry to Tetra-Substituted Heterodimeric and Homochiral Cyclobutanes.

J. McNulty, H. Jenkins, Alexander J. Nielsen, 2016, Chemistry.

Direct formation of esters and amides from carboxylic acids using diethyl chlorophosphate in pyridine

A. Robertson, J. McNulty, V. Krishnamoorthy, 2008 .

Development of a one-pot method for the homologation of aldehydes to carboxylic acids

J. McNulty, P. Das, 2009 .

Enantioselective Total Synthesis of the Proposed Structure of the Endophytic Fungal Metabolite Phomolide G: Structural Revision and Unambiguous Stereochemical Assignment

J. McNulty, H. Jenkins, David C. McLeod, 2016 .

A Practical Synthesis of (2S, 3R)‐3‐Amino‐2‐methylpentanoic Acid from L‐Aspartic Acid

J. McNulty, C. W. Jefford, 1994 .

Lipase-catalyzed stereoselective resolution and desymmetrization of binaphthols

D. Johnson, J. McNulty, A. Capretta, 2003 .

Dimethylmalonyltrialkylphosphoranes: new general reagents for esterification reactions allowing controlled inversion or retention of configuration on chiral alcohols.

A. Robertson, J. McNulty, A. Capretta, 2003, The Journal of organic chemistry.

Cancer Cell Mitochondria Targeting by Pancratistatin Analogs is Dependent on Functional Complex II and III

T. Hudlický, J. McNulty, S. Pandey, 2017, Scientific Reports.

Pancratistatin induces apoptosis in clinical leukemia samples with minimal effect on non-cancerous peripheral blood mononuclear cells

J. McNulty, S. Pandey, C. Hamm, 2010, Cancer Cell International.

Diastereoselective intramolecular nitroaldol entry to lycoricidine alkaloids

J. McNulty, R. Mo, 1998 .

On the direct 2,3-hydroxyl-group differentiation of tartaric acid esters

J. McNulty, J. Mao, 2002 .

Stereoselective Wittig Olefination Reactions Employing a Novel ortho‐P‐Aryl Alkoxide Effect.

J. McNulty, K. Keskar, 2009 .

Chemoenzymatic Synthesis of the Antifungal Compound (-)-Pestynol by a Convergent, Sonogashira Construction of the Central Yne-Diene

T. Hudlický, Manoj Kumar, J. McNulty, 2018, European Journal of Organic Chemistry.

High yielding synthesis of carboranes under mild reaction conditions using a homogeneous silver(I) catalyst: direct evidence of a bimetallic intermediate.

Afaf R. Genady, J. Valliant, J. Ioppolo, 2014, Angewandte Chemie.

A Simple, High-Yielding Synthesis of N-t-Butoxycarbonyl α-Amino Esters: Precursors for α-Amino Aldehydes

J. McNulty, I. V. Still, 1992 .

Dimethylmalonyltrialkylphosphoranes: probing the steric effect on phosphorus and its stereochemical consequence in esterification reactions of chiral secondary alcohols

S. Zavorine, J. Britten, A. Robertson, 2005 .

Total Enantioselective Synthesis of the Endophytic Fungal Polyketide Phomolide H and Its Structural Revision

J. McNulty, David C. McLeod, 2017 .

A direct synthesis of vinylphosphonium salts from alpha-trimethylsilyl ylides and non-enolizable aldehydes.

J. McNulty, P. Das, 2008, Chemistry.

An Improved Synthesis of α‐Phosphonoenamines Based on a Modified Peterson Olefination.

J. McNulty, P. Das, D. Gosciniak, 2008 .

Rapid and efficient entry to vinyl silanes from aldehydes employing a novel metalation-Peterson sequence.

J. McNulty, P. Das, 2008, Chemical communications.

Phosphaadamantanes as ligands for palladium catalyzed cross-coupling chemistry: library synthesis, characterization, and screening in the Suzuki coupling of alkyl halides and tosylates containing beta-hydrogens with boronic acids and alkylboranes.

J. Britten, A. Robertson, J. McNulty, 2004, The Journal of organic chemistry.

A new structural motif for rigid C2-symmetrical propeller-shaped 1,2-diamines employing double aromatic pi-stacking.

J. McNulty, A. Capretta, C. Frampton, 2001, Chemical communications.

Synthesis of α-methylstilbenes using an aqueous Wittig methodology and application toward the development of potent human aromatase inhibitors.

D. Crankshaw, J. McNulty, A. Holloway, 2019, Bioorganic & medicinal chemistry letters.

Enantioselective organocatalytic Michael/aldol sequence: anticancer natural product (+)-trans-dihydrolycoricidine.

J. McNulty, C. Zepeda-Velázquez, 2014, Angewandte Chemie.

Palladium complexes of 1,3,5,7-tetramethyl-2,4,8-trioxa-6-phenyl-6-phosphaadamantane: synthesis, crystal structure and use in the Suzuki and Sonogashira reactions and the alpha-arylation of ketones.

A. Robertson, J. McNulty, A. Capretta, 2004, The Journal of organic chemistry.

Structure-activity studies on the lycorine pharmacophore: A potent inducer of apoptosis in human leukemia cells

J. McNulty, S. Pandey, J. Bastida, 2009, Phytochemistry.

Pancratistatin induces apoptosis and autophagy in metastatic prostate cancer cells.

J. McNulty, S. Pandey, C. Griffin, 2011, International journal of oncology.

Pancratistatin Selectively Targets Cancer Cell Mitochondria and Reduces Growth of Human Colon Tumor Xenografts

J. McNulty, Aditya Karnik, S. Pandey, 2011, Molecular Cancer Therapeutics.

An iterative approach toward the synthesis of discrete oligomeric p-phenylene vinylene organic dyes employing aqueous Wittig chemistry

J. McNulty, David C. McLeod, 2011 .

Three new polyketides from fruiting bodies of the endophytic ascomycete Xylaria polymorpha

D. Liscombe, J. McNulty, Carla E. Brown, 2018, Natural product research.

A Catalytic, Oxidative Synthesis of Olivetol, Methyl Olivetolate and Orthogonally Protected Methyl Ether Derivatives

R. Carlini, J. McNulty, David Hurem, 2021 .

Identification of haemanthamine as a phytotoxic alkaloid in Narcissus pseudonarcissus L. (Daffodil) emerging buds.

M. Kumar, D. Liscombe, J. McNulty, 2023, Natural product research.

Discovery of a new class of cinnamyl-triazole as potent and selective inhibitors of aromatase (cytochrome P450 19A1).

D. Crankshaw, J. McNulty, A. Holloway, 2014, Bioorganic & medicinal chemistry letters.

Generation of three-dimensional human neuronal cultures: application to modeling CNS viral infections

R. Yolken, C. Chu, Nicholas M. Radio, 2018, Stem Cell Research & Therapy.

Comparison of three cell-based drug screening platforms for HSV-1 infection.

R. Yolken, M. Schurdak, P. Piazza, 2017, Antiviral research.

Studies directed towards the refinement of the pancratistatin cytotoxic pharmacophore.

M. Boyd, D. L. Herald, J. McNulty, 2001, Bioorganic & medicinal chemistry letters.

Isolation, Synthesis, and Semisynthesis of Amaryllidaceae Constituents from Narcissus and Galanthus sp.: De Novo Total Synthesis of 2- epi-Narciclasine.

T. Hudlický, D. Liscombe, J. McNulty, 2018, Journal of Natural Products.

Synthetic Approaches to the Naturally Occurring Anticancer Amaryllidaceae Alkaloids trans-dihydrolycoricidine and trans-dihydronarciclasine

J. McNulty, C. Zepeda-Velázquez, 2017 .

Discovery of a novel class of aldol-derived 1,2,3-triazoles: potent and selective inhibitors of human cytochrome P450 19A1 (aromatase).

D. Crankshaw, J. McNulty, A. Holloway, 2012, Bioorganic & medicinal chemistry letters.

Structure Activity Studies on the Crinane Alkaloid Apoptosis-inducing Pharmacophore

J. McNulty, S. Pandey, J. Bastida, 2009, Natural product communications.

Pancratistatin causes early activation of caspase-3 and the flipping of phosphatidyl serine followed by rapid apoptosis specifically in human lymphoma cells

J. McNulty, S. Pandey, N. Kekre, 2005, Cancer Chemotherapy and Pharmacology.

Heck reactions of aryl halides in phosphonium salt ionic liquids: library screening and applications

James McNulty, Alfredo Capretta, A. Robertson, 2004 .

Asymmetric Entry into 10b-aza-Analogues of Amaryllidaceae Alkaloids Reveals a Pronounced Electronic Effect on Antiviral Activity

V. Nimgaonkar, J. Britten, N. H. Werstiuk, 2018, ACS omega.

Investigation of aryl halides as ketone bioisosteres: refinement of potent and selective inhibitors of human cytochrome P450 19A1 (aromatase).

D. Crankshaw, J. McNulty, A. Holloway, 2013, Bioorganic & medicinal chemistry letters.

A scalable process for the synthesis of (E)-pterostilbene involving aqueous Wittig olefination chemistry

J. McNulty, David C. McLeod, 2013 .

Polyphenolic natural products and natural product–inspired steroidal mimics as aromatase inhibitors

J. McNulty, Alexander J. Nielsen, 2018, Medicinal research reviews.

Synergy of pancratistatin and tamoxifen on breast cancer cells in inducing apoptosis by targeting mitochondria

J. McNulty, S. Pandey, C. Griffin, 2008, Cancer biology & therapy.

Pancratistatin: A natural anti-cancer compound that targets mitochondria specifically in cancer cells to induce apoptosis

J. McNulty, N. Kekre, S. Pandey, 2005, Apoptosis.

A flavin-dependent monooxygenase produces nitrogenous tomato aroma volatiles using cysteine as a nitrogen source

H. Klee, D. Tieman, C. Goulet, 2022, Proceedings of the National Academy of Sciences.

Direct Formation of Esters and Amides from Carboxylic Acids Using Diethyl Chlorophosphate in Pyridine.

A. Robertson, J. McNulty, V. Krishnamoorthy, 2009 .

Tris(3-hydroxypropyl)phosphine (THPP): A mild, air-stable reagent for the rapid, reductive cleavage of small-molecule disulfides.

J. McNulty, Dino Amoroso, Michael Moser, 2015, Bioorganic & medicinal chemistry letters.

Palmitoyl‐dl‐Carnitine is a Multitarget Inhibitor of Pseudomonas aeruginosa Biofilm Development

L. Burrows, Gerard D. Wright, J. McNulty, 2011, Chembiochem : a European journal of chemical biology.

Human cytochrome P450 liability studies of trans-dihydronarciclasine: a readily available, potent, and selective cancer cell growth inhibitor.

D. Crankshaw, J. McNulty, A. Holloway, 2011, Journal of natural products.

Diastereoselective Pictet–Spengler reactions of L-(Boc)phenylalaninal and L-(Boc)prolinal: biomimetic syntheses of eudistomin T and (–)-woodinine

J. McNulty, I. V. Still, 1994 .

Amine- and sulfonamide-promoted Wittig olefination reactions in water.

J. McNulty, David C. McLeod, 2011, Chemistry.

Metabolite profiling reveals a role for intercellular dihydrocamalexic acid in the response of mature Arabidopsis thaliana to Pseudomonas syringae.

Daniel C. Wilson, D. Liscombe, J. McNulty, 2021, Phytochemistry.

Synthetic Approaches to the Eudistomin Marine Alkaloids

J. McNulty, I. V. Still, 2000 .

Review of Cytotoxic CA4 Analogues that Do Not Target Microtubules: Implications for CA4 Development.

J. McNulty, S. Pandey, D. Tarade, 2017, Mini reviews in medicinal chemistry.

Regioselective Ylide Formation on Acetal-Functionalized Trialkyl Phosphonium Salts: Extending the Scope of Carbonyl Homologation

J. McNulty, David Hurem, Arkesh Narayanappa, 2017, Synlett.

Phosphonium Salts as Room‐Temperature Ionic Liquids in Organic Synthesis

James McNulty, Alfredo Capretta, J. Clyburne, 2006 .

Sensitization of human melanoma cells by tamoxifen to apoptosis induction by pancratistatin, a nongenotoxic natural compound

J. McNulty, S. Chatterjee, S. Pandey, 2011, Melanoma research.