850209-49-3Relevant academic research and scientific papers
Facile synthesis of alkyl 1-oxo-3-phenyl-1H-indene-2-earboxylate through palladium-catalyzed carboalkoxylation from 2-bromo-3-phenylinden-1-ones
Yum, Eul Kgun,Park, Woul Seong,Kim, Se Hoan,Kang, Seung Kyu,Kim, Sung Soo,Ahn, Jin Hee
supporting information; experimental part, p. 1068 - 1069 (2009/12/03)
Palladium-catalyzed carboalkoxylation of 2-bromo-3-phenylindenones in various alcoholic solvents afforded diverse alkyl 1-oxo-3-phenyl-1H-indene-2- carboxylates in high yields. Copyright
Indenone derivatives: A novel template for peroxisome proliferator- activated receptor γ (PPARγ) agonists
Ahn, Jin Hee,Shin, Mi Sik,Jung, Sun Ho,Kang, Seung Kyu,Kim, Kwang Rok,Rhee, Sang Dal,Jung, Won Hoon,Yang, Sung Don,Kim, Seung Jun,Woo, Joo Rang,Lee, Jeong Hyung,Cheon, Hyae Gyeong,Kim, Sung Soo
, p. 4781 - 4784 (2007/10/03)
Agonists of peroxisome proliferator-activated receptor γ(PPAR γ) are of interest as a treatment for diabetes, which prompted the identification of a new class of non-TZD PPAR γ agonist. Moreover, compound 14c has displayed the most active agonistic activi
The synthesis, structural characterization and photochemistry of some 3-phenylindenones
Seery, Michael K.,Draper, Sylvia M.,Kelly, John M.,McCabe, Thomas,McMurry, T. Brian H.
, p. 470 - 474 (2007/10/03)
The synthesis of 3-phenylindenone (1a), 6-methoxy-3-phenylindenone (1b), 2-bromo-6-methoxy-3-phenylindenone (1c) and 2-ethoxycarbonyl-6-methoxy-3- phenylindenone (1d) is described using two methods - synthesis via indanone precursors and synthesis via pro
INDENE DERIVATIVES AND PROCESS FOR THE PREPARATION THEREOF
-
Page/Page column 23-24, (2008/06/13)
The inventive indene derivatives of formula (I) are capable of selectively modulating the activities of peroxisome proliferator activated receptors (PPARs), causing no adverse side effects, and thus, they are useful for the treatment and prevention of dis
