Minatti, Ana; Zheng, Xiaolai; Buchwald, Stephen L. published the artcile< Synthesis of Chiral 3-Substituted Indanones via an Enantioselective Reductive-Heck Reaction>, Quality Control of 112-63-0, the main research area is indanone aryl asym synthesis; chalcone sulfonyloxy preparation stereoselective reductive Heck.
An efficient intramol. palladium-catalyzed, asym. reductive Heck reaction has been developed, which allowed for the synthesis of either enantiomerically enriched 3-substituted indanones I [X = H2; R1 = H, 6-MeO, 4-Me, 4-Me3Si, 5,6-(MeO)2, 6,7-benzo; R2 = Ph, 4-ClC6H4, 4-MeOC6H4, 3,4-Cl2C6H3, piperonyl, 2-furyl, ferrocenyl] or α-exo-methylene indanones I (X = CH2) from chalcones II (R3 = F3C, n-C4F9) depending on the base used.
Journal of Organic Chemistry published new progress about Alkyl aryl ketones Role: SPN (Synthetic Preparation), PREP (Preparation). 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, Quality Control of 112-63-0.
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics