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56: Multiple RTK targeting as a therapeutic option in malignant pleural mesothelioma

Lung cancer (Amsterdam, Netherlands), 2017, Vol.103, p.S26-S26

2017

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86 When RON MET TAM: potential interventions for mesothelioma therapy

Lung cancer (Amsterdam, Netherlands), 2016, Vol.91, p.S31-S31

2016

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79 The RON (MST1R)/MSP pathway is a potential therapeutic target in malignant pleural mesothelioma

Lung cancer (Amsterdam, Netherlands), 2014, Vol.83, p.S29-S30

2014

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Targeting the RON/MET/TAM signalling network in mesothelioma

Annals of oncology, 2017-04, Vol.28, p.ii56

2017

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P1.09-007 Targeting MET/TAM Receptors in Mesothelioma: Are Multi-TKIs Superior to Specific TKI?

Journal of thoracic oncology, 2017-11, Vol.12 (11), p.S2020-S2020

2017

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Lewis acid-catalyzed Mannich type reactions with potassium organotrifluoroborates

Tetrahedron letters, 2004-04, Vol.45 (17), p.3471-3474

2004

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Amphoteric Character of 2-Vinyloxiranes: Synthetic Equivalents of β,γ-Unsaturated Aldehydes and a Vinylogous Enolate

Angewandte Chemie (International ed.), 2000-11, Vol.39 (22), p.4079-4082

2000

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Straightforward Access to [6]Metacyclophene-based Enynes by an Inter-Intramolecular Tandem Etherification through a One-Pot Double SNAr Reaction

Synlett, 2000-06, Vol.2000 (6), p.0874-0876

2000

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Practical synthesis of acetophenones from phenoltriflates

Tetrahedron letters, 2001-01, Vol.42 (2), p.265-266

2001

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Novel Exploration of the SNAr Reaction

Synlett, 1998, Vol.1998 (7), p.794-796

1998

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Towards a New Type of Aromatic Diynes Activation: Synthesis of a Novel Bicyclic Enediyne

Synlett, 1998-05, Vol.1998 (5), p.537-539

1998

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An Alternative Synthesis of Both Enantiomers of trans-3,4-Bis(benzyloxy)cyclopentanone

Synlett, 1997-09, Vol.1997 (9), p.1061-1062

1997

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Amphoteric Character of 2-Vinyloxiranes: Synthetic Equivalents of beta,gamma-Unsaturated Aldehydes and a Vinylogous Enolate We thank Professor Batey and his group for providing the allyl and crotyltrifluoroborates. This work was supported by the National Science and Engineering Research Council (NSERC) and the University of Toronto. S.G.O. thanks NSERC for a post-graduate scholarship

Angewandte Chemie International Edition, 2000-11, Vol.39 (22), p.4079-4082

2000

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Synthesis of 5-/10-Membered Ring Analogues of the Dienediyne Core of Neocarzinostatine Chromophore by Palladium(0)-Mediated Ring-Closure Reaction

Liebigs Annalen, 1996-04, Vol.1996 (4), p.447-456

1996

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ChemInform Abstract: Novel Exploration of the S N Ar Reaction

ChemInform, 1998-10, Vol.29 (43)

1998

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ChemInform Abstract: Novel Exploration of the SNAr Reaction

ChemInform, 1998-10, Vol.29 (43), p.no-no

1998

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ChemInform Abstract: Towards a New Type of Aromatic Diynes Activation: Synthesis of a Novel Bicyclic Enediyne

ChemInform, 1998-08, Vol.29 (33), p.no-no

1998

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ChemInform Abstract: An Alternative Synthesis of Both Enantiomers of trans-3,4-Bis(benzyloxy)cyclopentanone

ChemInform, 1998-01, Vol.29 (3), p.no-no

1998

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ChemInform Abstract: Synthesis of 5-/10-Membered Ring Analogues of the Dienediyne Core of Neocarzinostatine Chromophore by Palladium(0)-Mediated Ring-Closure Reaction

ChemInform, 1996-08, Vol.27 (32), p.no-no

1996

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Gallenblasenpolypen: Ist der Nachweis eines Gefäßstiels eine Operationsindikation?

Ultraschall in der Medizin, 2006, Vol.27 (S 1)

2006

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Design and synthesis of close analogs of LCRF-0004, a potent and selective RON receptor tyrosine kinase inhibitor

Bioorganic & medicinal chemistry letters, 2015-06, Vol.25 (12), p.2527-2531

2015

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Design, synthesis and RON receptor tyrosine kinase inhibitory activity of new head groups analogs of LCRF-0004

Bioorganic & medicinal chemistry letters, 2015-09, Vol.25 (18), p.3810-3815

2015

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Design and synthesis of constrained analogs of LCRF-0004 as potent RON tyrosine kinase inhibitors

Bioorganic & medicinal chemistry letters, 2015-09, Vol.25 (17), p.3706-3710

2015

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An alignment-independent three-dimensional quantitative structure-activity relationship study on ron receptor tyrosine kinase inhibitors

Journal of bioinformatics and computational biology, 2022-06, Vol.20 (3), p.2250015

2022

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Active pre-atrophic autoimmune gastritis. A practice-oriented concept for diagnosis and treatment

Der Pathologe, 2001-01, Vol.22 (1), p.19-24

2001

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56: Multiple RTK targeting as a therapeutic option in malignant pleural mesothelioma

86 When RON MET TAM: potential interventions for mesothelioma therapy

79 The RON (MST1R)/MSP pathway is a potential therapeutic target in malignant pleural mesothelioma

Targeting the RON/MET/TAM signalling network in mesothelioma

P1.09-007 Targeting MET/TAM Receptors in Mesothelioma: Are Multi-TKIs Superior to Specific TKI?

Lewis acid-catalyzed Mannich type reactions with potassium organotrifluoroborates

Amphoteric Character of 2-Vinyloxiranes: Synthetic Equivalents of β,γ-Unsaturated Aldehydes and a Vinylogous Enolate

Straightforward Access to [6]Metacyclophene-based Enynes by an Inter-Intramolecular Tandem Etherification through a One-Pot Double SNAr Reaction

Practical synthesis of acetophenones from phenoltriflates

Novel Exploration of the SNAr Reaction

Towards a New Type of Aromatic Diynes Activation: Synthesis of a Novel Bicyclic Enediyne

An Alternative Synthesis of Both Enantiomers of trans-3,4-Bis(benzyloxy)cyclopentanone

Synthesis of 5-/10-Membered Ring Analogues of the Dienediyne Core of Neocarzinostatine Chromophore by Palladium(0)-Mediated Ring-Closure Reaction

ChemInform Abstract: Novel Exploration of the S N Ar Reaction

ChemInform Abstract: Novel Exploration of the SNAr Reaction

ChemInform Abstract: Towards a New Type of Aromatic Diynes Activation: Synthesis of a Novel Bicyclic Enediyne

ChemInform Abstract: An Alternative Synthesis of Both Enantiomers of trans-3,4-Bis(benzyloxy)cyclopentanone

ChemInform Abstract: Synthesis of 5-/10-Membered Ring Analogues of the Dienediyne Core of Neocarzinostatine Chromophore by Palladium(0)-Mediated Ring-Closure Reaction

Gallenblasenpolypen: Ist der Nachweis eines Gefäßstiels eine Operationsindikation?

Design and synthesis of close analogs of LCRF-0004, a potent and selective RON receptor tyrosine kinase inhibitor

Design, synthesis and RON receptor tyrosine kinase inhibitory activity of new head groups analogs of LCRF-0004

Design and synthesis of constrained analogs of LCRF-0004 as potent RON tyrosine kinase inhibitors

An alignment-independent three-dimensional quantitative structure-activity relationship study on ron receptor tyrosine kinase inhibitors

Active pre-atrophic autoimmune gastritis. A practice-oriented concept for diagnosis and treatment

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