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Chem
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August 28, 2023
Iron-mediated modular decarboxylative cross-nucleophile coupling
Grace A Lutovsky, Samuel N Gockel, Mark W Bundesmann, et al.
The Journal of Organic Chemistry
|
November 3, 2017
Spiropiperidine Sultam and Lactam Templates: Diastereoselective Overman Rearrangement and Metathesis followed by NH Arylation
Luis A Martinez-Alsina, John C Murray, Leanne M Buzon, et al.
ACS Medicinal Chemistry Letters
|
June 6, 2014
Measurement of atropisomer racemization kinetics using segmented flow technology
Jennifer E Davoren, Mark W Bundesmann, Qi T Yan, et al.
Nature Chemistry
|
January 6, 2022
Decarboxylative cross-nucleophile coupling via ligand-to-metal charge transfer photoexcitation of Cu(II) carboxylates
Qi Yukki Li, Samuel N Gockel, Grace A Lutovsky, et al.
Magnetic Resonance in Chemistry : MRC
|
July 30, 2016
Utilizing on- and off-line monitoring tools to follow a kinetic resolution step during flow synthesis
Kathleen A Farley, Usa Reilly, Dennis P Anderson, et al.
Angewandte Chemie (International Ed. in English)
|
September 30, 2017
Visible-Light-Initiated Manganese Catalysis for C-H Alkylation of Heteroarenes: Applications and Mechanistic Studies
Philippe Nuhant, Martins S Oderinde, Julien Genovino, et al.
Journal of Medicinal Chemistry
|
February 17, 2025
Conformational Role of Methyl in the Potency of Cyclohexane-Substituted Squaramide CCR6 Antagonists
Brian S Gerstenberger, Ray Unwalla, Kathleen A Farley, et al.
Journal of Medicinal Chemistry
|
October 3, 2012
Application of structure-based drug design and parallel chemistry to identify selective, brain penetrant, in vivo active phosphodiesterase 9A inhibitors
Michelle M Claffey, Christopher J Helal, Patrick R Verhoest, et al.
Journal of Medicinal Chemistry
|
March 18, 2015
Utilizing structures of CYP2D6 and BACE1 complexes to reduce risk of drug-drug interactions with a novel series of centrally efficacious BACE1 inhibitors
Michael A Brodney, Elizabeth M Beck, Christopher R Butler, et al.
Journal of Medicinal Chemistry
|
September 22, 2025
Discovery of PF-07054894, a Potent Squaramide-Based CCR6 Antagonist Displaying High CXCR2 Selectivity
Mark E Schnute, Huixian Wu, John I Trujillo, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Chem
|
August 28, 2023
Iron-mediated modular decarboxylative cross-nucleophile coupling
Grace A Lutovsky, Samuel N Gockel, Mark W Bundesmann, et al.
The Journal of Organic Chemistry
|
November 3, 2017
Spiropiperidine Sultam and Lactam Templates: Diastereoselective Overman Rearrangement and Metathesis followed by NH Arylation
Luis A Martinez-Alsina, John C Murray, Leanne M Buzon, et al.
ACS Medicinal Chemistry Letters
|
June 6, 2014
Measurement of atropisomer racemization kinetics using segmented flow technology
Jennifer E Davoren, Mark W Bundesmann, Qi T Yan, et al.
Nature Chemistry
|
January 6, 2022
Decarboxylative cross-nucleophile coupling via ligand-to-metal charge transfer photoexcitation of Cu(II) carboxylates
Qi Yukki Li, Samuel N Gockel, Grace A Lutovsky, et al.
Magnetic Resonance in Chemistry : MRC
|
July 30, 2016
Utilizing on- and off-line monitoring tools to follow a kinetic resolution step during flow synthesis
Kathleen A Farley, Usa Reilly, Dennis P Anderson, et al.
Angewandte Chemie (International Ed. in English)
|
September 30, 2017
Visible-Light-Initiated Manganese Catalysis for C-H Alkylation of Heteroarenes: Applications and Mechanistic Studies
Philippe Nuhant, Martins S Oderinde, Julien Genovino, et al.
Journal of Medicinal Chemistry
|
February 17, 2025
Conformational Role of Methyl in the Potency of Cyclohexane-Substituted Squaramide CCR6 Antagonists
Brian S Gerstenberger, Ray Unwalla, Kathleen A Farley, et al.
Journal of Medicinal Chemistry
|
October 3, 2012
Application of structure-based drug design and parallel chemistry to identify selective, brain penetrant, in vivo active phosphodiesterase 9A inhibitors
Michelle M Claffey, Christopher J Helal, Patrick R Verhoest, et al.
Journal of Medicinal Chemistry
|
March 18, 2015
Utilizing structures of CYP2D6 and BACE1 complexes to reduce risk of drug-drug interactions with a novel series of centrally efficacious BACE1 inhibitors
Michael A Brodney, Elizabeth M Beck, Christopher R Butler, et al.
Journal of Medicinal Chemistry
|
September 22, 2025
Discovery of PF-07054894, a Potent Squaramide-Based CCR6 Antagonist Displaying High CXCR2 Selectivity
Mark E Schnute, Huixian Wu, John I Trujillo, et al.
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