328029-93-2Relevant academic research and scientific papers
Organocatalytic oxa/aza-Michael-Michael cascade strategy for the construction of spiro [chroman/tetrahydroquinoline-3,3′-oxindole] scaffolds
Mao, Haibin,Lin, Aijun,Tang, Yang,Shi, Yan,Hu, Hongwen,Cheng, Yixiang,Zhu, Chengjian
supporting information, p. 4062 - 4065 (2013/09/12)
A new useful and effective chiral amine-catalyzed oxa-and aza-Michael-Michael cascade methodology for the construction of enantiomerically enriched indolinones spiro-fused with chromans or tetrahydroquinolines is reported. By employing suitable organocatalysts depending on the different Michael donors (Ar-OH/Ar-NHR), the processes offered excellent stereocontrol (dr >20:1, >99% ee) under mild conditions.
