28918-13-0Relevant academic research and scientific papers
Organocatalyzed biomimetic selective reduction of c=c double bonds of chalcones
Tripathi, Vishwa Deepak,Jha, Anand Mohan
, p. 2322 - 2324 (2018/09/09)
In this article, we reported a biomimetic approach for chemoselective reduction of C=C double bonds in chalcones under metal and acid free conditions, that relies on olefin activation by hydrogen bond formation. The process requires only catalytic amount of ephedrine as hydrogen bond donor and utilizes Hantzsch esters for transfer hydrogenation.
Rhodium(I)-catalyzed arylation of β-chloro ketones and related derivatives through domino dehydrochlorination/conjugate addition
Jiang, Quanbin,Guo, Tenglong,Wang, Qingfu,Wu, Ping,Yu, Zhengkun
supporting information, p. 1874 - 1880 (2013/07/19)
Highly efficient arylations of β-chloro ketones and their ester and amide derivatives were achieved by means of domino dehydrochlorination/Rh(I)- catalyzed conjugate addition. In situ generated vinyl ketones and their analogues were identified as the reaction intermediates. The present synthetic protocol provides a concise route to (chiral) β-aryl ketones, esters, and amides. Copyright
Branch-selective intermolecular hydroacylation: Hydrogen-mediated coupling of anhydrides to styrenes and activated olefins
Hong, Young-Taek,Barchuk, Andriy,Krische, Michael J.
, p. 6885 - 6888 (2007/10/03)
(Chemical Equation Presented) Branching out with hydrogen: Hydrogenation of symmetric or mixed carboxylic anhydrides in the presence of styrenes or activated olefins generates intermolecular hydroacylation products. The use of cationic rhodium catalysts ligated by triphenylarsine (Ph3As) results in the formation of branched coupling products as single regioisomers in high yields (see scheme; cod = cycloocta-1,5-diene, ArF = 3,5-(CF 3)2C6H3).
