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Development of an allosteric inhibitor class blocking RNA elongation by the respiratory syncytial virus polymerase complex

The Journal of biological chemistry, 2018-10, Vol.293 (43), p.16761-16777

2018

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First Experimental and Theoretical Evidence of a Deactivating Enone Dienophile in the Transannular Diels−Alder Reaction

Journal of organic chemistry, 2003-03, Vol.68 (6), p.2390-2397

2003

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Novel spirothiazamenthane inhibitors of the influenza A M2 proton channel

European journal of medicinal chemistry, 2016-09, Vol.120, p.64-73

2016

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Corrigendum to “Assessing the oral bioavailability of difluorosialic acid prodrugs, potent viral neuraminidase inhibitors, using a snapshot PK screening assay” [Bioorg. Med. Chem. Lett. 25 (2015) 2505–2509]

Bioorganic & medicinal chemistry letters, 2016-08, Vol.26 (15), p.3830-3830

2016

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Assessing the oral bioavailability of difluorosialic acid prodrugs, potent viral neuraminidase inhibitors, using a snapshot PK screening assay

Bioorganic & medicinal chemistry letters, 2015-06, Vol.25 (12), p.2505-2509

2015

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Design of Substituted Imidazolidinylpiperidinylbenzoic Acids as Chemokine Receptor 5 Antagonists: Potent Inhibitors of R5 HIV‑1 Replication

Journal of medicinal chemistry, 2013-10, Vol.56 (20), p.8049-8065

2013

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Prospective CCR5 Small Molecule Antagonist Compound Design Using a Combined Mutagenesis/Modeling Approach

Journal of the American Chemical Society, 2011-10, Vol.133 (41), p.16477-16485

2011

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Design and synthesis of pyridin-2-ylmethylaminopiperidin-1-ylbutyl amide CCR5 antagonists that are potent inhibitors of M-tropic (R5) HIV-1 replication

Bioorganic & medicinal chemistry letters, 2011-12, Vol.21 (23), p.6950-6954

2011

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Design and synthesis of pyridin-2-yloxymethylpiperidin-1-ylbutyl amide CCR5 antagonists that are potent inhibitors of M-tropic (R5) HIV-1 replication

Bioorganic & medicinal chemistry letters, 2011-04, Vol.21 (8), p.2450-2455

2011

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Mitigating hERG Inhibition: Design of Orally Bioavailable CCR5 Antagonists as Potent Inhibitors of R5 HIV-1 Replication

ACS medicinal chemistry letters, 2012-03, Vol.3 (3), p.216-221

2012

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Synthesis of the C14-C28 Fragment of Tetronasin

Synthesis (Stuttgart), 2005-12, Vol.2005 (19), p.3219-3224

2005

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Progress toward the Total Synthesis of Cassaine via the Transannular Diels−Alder Strategy

Organic letters, 2000-12, Vol.2 (26), p.4149-4152

2000

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The Exocyclic Effect: Protecting Group Strategy to Enhance Stereoselectivity in Hydrogen Transfer Reactions of Acyclic Free Radicals

Journal of organic chemistry, 1997-12, Vol.62 (26), p.9276-9283

1997

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Etude de la réaction de Diels -Alder transannulaire de macrocycles à quatorze membres de géométrie trans-trans-trans comportant un diénophile activé ou non-activé

Bourque, Elyse

2001

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Synthetic applications of planar chiral cationic η3-allylmolybdenum complexes

Pure and applied chemistry, 2004-01, Vol.76 (3), p.477-494

2004

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Synthesis of the C14-C28 Fragment of Tetronasin

ChemInform, 2006-05, Vol.37 (18), p.no-no

2006

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ChemInform Abstract: Progress Toward the Total Synthesis of Cassaine via the Transannular Diels-Alder Strategy

ChemInform, 2001-04, Vol.32 (16), p.no-no

2001

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Macrocyclic Studies of EZ and ZZ 12-membered Aza Macrocycles; Novel Molecular Rearrangement Observed

Synlett, 1999-07, Vol.1999 (7), p.1115-1117

1999

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Longitudinal Study of Lactococcus Phages in a Canadian Cheese Factory

Applied and environmental microbiology, 2023-05, Vol.89 (5), p.e0042123-e0042123

2023

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Development of an allosteric inhibitor class blocking RNA elongation by the respiratory syncytial virus polymerase complex

First Experimental and Theoretical Evidence of a Deactivating Enone Dienophile in the Transannular Diels−Alder Reaction

Novel spirothiazamenthane inhibitors of the influenza A M2 proton channel

Corrigendum to “Assessing the oral bioavailability of difluorosialic acid prodrugs, potent viral neuraminidase inhibitors, using a snapshot PK screening assay” [Bioorg. Med. Chem. Lett. 25 (2015) 2505–2509]

Assessing the oral bioavailability of difluorosialic acid prodrugs, potent viral neuraminidase inhibitors, using a snapshot PK screening assay

Design of Substituted Imidazolidinylpiperidinylbenzoic Acids as Chemokine Receptor 5 Antagonists: Potent Inhibitors of R5 HIV‑1 Replication

Prospective CCR5 Small Molecule Antagonist Compound Design Using a Combined Mutagenesis/Modeling Approach

Design and synthesis of pyridin-2-ylmethylaminopiperidin-1-ylbutyl amide CCR5 antagonists that are potent inhibitors of M-tropic (R5) HIV-1 replication

Design and synthesis of pyridin-2-yloxymethylpiperidin-1-ylbutyl amide CCR5 antagonists that are potent inhibitors of M-tropic (R5) HIV-1 replication

Mitigating hERG Inhibition: Design of Orally Bioavailable CCR5 Antagonists as Potent Inhibitors of R5 HIV-1 Replication

Synthesis of the C14-C28 Fragment of Tetronasin

Progress toward the Total Synthesis of Cassaine via the Transannular Diels−Alder Strategy

The Exocyclic Effect: Protecting Group Strategy to Enhance Stereoselectivity in Hydrogen Transfer Reactions of Acyclic Free Radicals

Etude de la réaction de Diels -Alder transannulaire de macrocycles à quatorze membres de géométrie trans-trans-trans comportant un diénophile activé ou non-activé

Synthetic applications of planar chiral cationic η3-allylmolybdenum complexes

Synthesis of the C14-C28 Fragment of Tetronasin

ChemInform Abstract: Progress Toward the Total Synthesis of Cassaine via the Transannular Diels-Alder Strategy

Macrocyclic Studies of EZ and ZZ 12-membered Aza Macrocycles; Novel Molecular Rearrangement Observed

Longitudinal Study of Lactococcus Phages in a Canadian Cheese Factory

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