222622-82-4Relevant academic research and scientific papers
Membrane receptor probes: Solid-phase synthesis of biotin-Asp-PEG-arvanil derivatives
Visintin, Cristina,Aliev, Abil E.,Riddall, Dieter,Baker, David,Okuyama, Masahiro,Hoi, Pui Man,Hiley, Robin,Selwood, David L.
, p. 1699 - 1702 (2005)
(Chemical Equation Presented) A modular, flexible solid-phase synthetic route for the preparation of biotinylated cross-linking probes of membrane receptors is described. The route utilizes an orthogonal protection strategy employing a Pd[0] cleavable all
NOVEL CARBONATE ANALOGUES BEARING PTEROSTILBENE AMINO ACIDS FOR THE TREATMENT OF NON-ALCOHOLIC FATTY LIVER DISEASE AND NON-ALCOHOLIC STEATOHEPATITIS
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Page/Page column 30-31, (2021/12/31)
A series of novel analogs of water soluble pterostilbene amino acid bearing carbonates were synthesized, which show activities in treating a non-alcoholic fatty liver disease and a nonalcoholic steatohepatitis (NASH).
Catalytic Alkyne Arylation Using Traceless Directing Groups
Park, Jung-Woo,Kang, Bubwoong,Dong, Vy M.
supporting information, p. 13598 - 13602 (2018/09/25)
By using Pd0/Mandyphos, we achieved a three-component aminoarylation of alkynes to generate enamines, which are then hydrolyzed to either α-arylphenones or α,α-diarylketones. This Pd-catalyzed method overcomes established known pathways to enable the use of amines as traceless directing groups for C?C bond formation.
