137933-01-8Relevant academic research and scientific papers
Potassium tert-butoxide mediated Heck-type cyclization/isomerization- benzofurans from organocatalytic radical cross-coupling reactions
Rueping, Magnus,Leiendecker, Matthias,Das, Arindam,Poisson, Thomas,Bui, Lan
supporting information; experimental part, p. 10629 - 10631 (2011/10/30)
A transition metal-free Heck-type cyclization/isomerization reaction has been developed. Mediated by potassium tert-butoxide and phenanthroline a variety of benzofuran derivatives have been synthesized.
Design and synthesis of novel PPARα/γ/δ triple activators using a known PPARα/γ dual activator as structural template
Mogensen, John P.,Jeppesen, Lone,Bury, Paul S.,Pettersson, Ingrid,Fleckner, Jan,Nehlin, Jan,Frederiksen, Klaus S.,Albrektsen, Tatjana,Din, Nanni,Mortensen, Steen B.,Svensson, L. Anders,Wassermann, Karsten,Wulff, Erik M.,Ynddal, Lars,Sauerberg, Per
, p. 257 - 260 (2007/10/03)
Using a known dual PPARα/γ activator (5) as a structural template, SAR evaluations led to the identification of triple PPARα/γ/δ activators (18-20) with equal potency and efficacy on all three receptors. These compounds could become useful tools for studying the combined biological effects of PPARα/γ/δ activation.
Palladium catalyzed cyclocarbonylation of 3,3-diarylallyl acetates
Iwasaki, Masakazu,Ishii, Youichi,Hidai, Masanobu
, p. 435 - 442 (2007/10/02)
Palladium-catalyzed cyclocarbonylation of 3,3-diarylallyl acetates afforded 4-aryl-substituted 1-naphthyl acetates where the cyclization occurred selectively on the more electron-rich ring.
