7433-92-3Relevant articles and documents
Palladium-Catalyzed Double Carbonylative Cyclization of Benzoins: Synthesis and Photoluminescence of Bis-Ester-Bridged Stilbenes
Tani, Yosuke,Ogawa, Takuji
supporting information, p. 7442 - 7446 (2019/01/03)
A palladium-catalyzed double carbonylative cyclization of benzoins has been developed, which realizes the synthesis of bis-ester-bridged stilbenes just in two steps from aldehydes. Thus, the obtained fully fused tetracyclic π-systems have a pyrano[3,2-b]pyran-2,6-dione (PPD) core on their center, showing two reversible reductions at low potentials. In addition, their photoluminescence properties are strikingly affected by the aromatic rings fused to the PPD core; bis-thieno-fused PPDs are found to be excellent fluorophores with quantum yields up to 0.98.
ELECTROCHEMICAL REDUCTION OF PHTHALYL CHLORIDE. A NEW ROUTE FOR THE SYNTHESIS OF 3-SUBSTITUTED PHTHALIDES
Guirado, Antonio,Barba, Fructuoso,Hursthouse, Michael B.,Martinez, Antonio,Arcas, Aurelia
, p. 4063 - 4066 (2007/10/02)
The cathodic reduction, under various conditions, of phthalyl chloride enables efficient synthesis of (E)-biisobenzofuranyliden-3,3'-dion(4), (2)-benzopyrano - benzopyrano-6,12-dione (7), 3-chlorophtalide (8), phtalide (9), or (E)-3 phtalide (12); the structure of the latter compound was confirmed by X-ray crystallography.