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Organic Letters|September 24, 2005
A mild thermal and acid-catalyzed rearrangement of O-aryl ethers into ortho-hydroxy arenesFrederick W Goldberg, Philip Magnus, Rachel TurnbullACS Medicinal Chemistry Letters|February 21, 2019
Evolution of Small Molecule Kinase DrugsHelen L Lightfoot, Frederick W Goldberg, Joerg SedelmeierJournal of Medicinal Chemistry|December 4, 2013
Medicinal chemistry of inhibitors of 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD1)James S Scott, Frederick W Goldberg, Andrew V TurnbullOrganic & Biomolecular Chemistry|May 9, 2012
Asymmetric synthesis of 2-alkyl-substituted tetrahydroquinolines by an enantioselective aza-Michael reactionLaura L Taylor, Frederick W Goldberg, King Kuok Mimi HiiDrug Discovery Today|October 5, 2014
Designing novel building blocks is an overlooked strategy to improve compound qualityFrederick W Goldberg, Jason G Kettle, Thierry Kogej, et al.Journal of the American Chemical Society|September 21, 2007
An expedient formal total synthesis of (-)-diazonamide A via a powerful, stereoselective O-aryl to C-aryl migration to form the C10 quaternary centerChi-Ming Cheung, Frederick W Goldberg, Philip Magnus, et al.Chemical Communications (Cambridge, England)|September 4, 2013
Aziridine-based concise synthesis of (±)-alstonerineDonald Craig, Frederick W Goldberg, Richard W Pett, et al.Drug Discovery Today|July 30, 2009
The changing landscape of cancer drug discovery: a challenge to the medicinal chemist of tomorrowKlaus Pors, Frederick W Goldberg, Christopher P Leamon, et al.Angewandte Chemie (International Ed. in English)|November 20, 2023
α-Functionalisation of Cyclic Sulfides Enabled by Lithiation TrappingNico Seling, Masakazu Atobe, Kevin Kasten, et al.Journal of Medicinal Chemistry|November 17, 2012
Free-Wilson and structural approaches to co-optimizing human and rodent isoform potency for 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD1) inhibitorsFrederick W Goldberg, Andrew G Leach, James S Scott, et al.Pageof 3