61799-53-9Relevant academic research and scientific papers
Enantioselective Synthesis of Isoxazolines Enabled by Palladium-Catalyzed Carboetherification of Alkenyl Oximes
Chen, Mingjie,Li, Wenbo,Wang, Lei,Wang, Yuzhuo,Zhang, Junliang,Zhang, Kenan
supporting information, p. 4421 - 4427 (2020/02/11)
Reported here is a highly efficient Pd/Xiang-Phos catalyzed enantioselective carboetherification of alkenyl oximes with either aryl or alkenyl halides, delivering various chiral 3,5-disubstituted and 3,5,5-trisubstituted isoxazolines in good yields with u
Carbon-carbon bond forming reactions of η3-allyl iron tricarbonyl anions with carbon electrophiles
Chang, Seok,Yoon, Jaeyon,Brookbart, Maurice
, p. 1869 - 1879 (2007/10/02)
Reaction of the η3-allyl iron tricarbonyl anion, 1, with alkyl halides (RX, R = -CH3, -CH2Ph, -(CH2)3CH3, -CH(CH3)2,-CH2CH=CH2) followed by treat
Electrochemical synthesis of ketones from acid chlorides and alkyl and aryl halides catalysed by nickel complexes
Marzouk, H.,Rollin, Y.,Folest, J. C.,Nedelec, J. Y.,Perichon, J.
, p. C47 - C50 (2007/10/02)
The nickel-catalysed electrochemical cross-coupling of acid chlorides and alkyl or aryl halides in acetonitrile affords unsymmetric ketones in good to high yields.The reaction can be performed under very simple and mild conditions in a diaphragmless cell.A zinc rod as the sacrificial anode has been found to be the most efficient.
RING OPENING OF BENZOXAZOLES WITH ALLYLIC GRIGNARD REAGENTS: SYNTHESIS OF N-DIALLYLALKYL-o-AMINOPHENOLS.
Florio, Saverio,Epifani, Erbana,Ingrosso, Giovanni,Sgarra, Riccardo
, p. 5089 - 5096 (2007/10/02)
The title benzoxales 1a-d react cleanly with allylic Grignard reagents 2a-c undergoing ring opening to give good yields of N-diallyl-alkyl-o-aminophenols 3a-m.A plausible mechanism is discussed.
