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Synthesis of 3‑(Hetero)aryl Tetrahydropyrazolo[3,4‑c]pyridines by Suzuki–Miyaura Cross-Coupling Methodology
American Chemical Society | 2014| -
Chemical Biology Approaches Confirm MCT4 as the Therapeutic Target of a Cellular Optimized Hit
American Chemical Society | 2023| -
Discovery of Clinical Candidate AZD0095, a Selective Inhibitor of Monocarboxylate Transporter 4 (MCT4) for Oncology
American Chemical Society | 2023| -
Optimization of hERG and Pharmacokinetic Properties for Basic Dihydro‑8H‑purin-8-one Inhibitors of DNA-PK
American Chemical Society | 2022| -
Identification and optimisation of 7-azaindole PAK1 inhibitors with improved potency and kinase selectivity
National licenceRoyal Society of Chemistry | 2014| -
Synthesis of Benzyl Alcohol Building Blocks Bearing an Aldehyde, Pinacol Borane or Carboxylic Acid Motif via Lithium–Bromide Exchange
Online Contents | 2014|Contributors: Lamont, Gillian M. -
Optimized scale up of 3-pyrimidinylpyrazolo[1,5-a]pyridine via Suzuki coupling; a general method of accessing a range of 3-(hetero)arylpyrazolo[1,5-a]pyridines
Online Contents | 2012|Contributors: Lamont, Gillian M. -
Synthesis of 3-(Hetero)aryl Tetrahydropyrazolo[3,4-c]pyridines by Suzuki–Miyaura Cross-Coupling Methodology
Online Contents | 2014|Contributors: Lamont, Gillian M. -
Discovery of AZD4747, a Potent and Selective Inhibitor of Mutant GTPase KRASG12C with Demonstrable CNS Penetration
American Chemical Society | 2023| -
Sulfonyl-morpholino-pyrimidines: SAR and development of a novel class of selective mTOR kinase inhibitor
Online Contents | 2012|Contributors: Lamont, Gillian M.
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