1608094-84-3Relevant academic research and scientific papers
Enantioselective organocatalytic synthesis of the chiral chromenes by domino oxa-Michael-aldol reaction
Pendalwar, Shrikant S.,Chakrawar, Avinash V.,Bhusare, Sudhakar R.
, p. 942 - 944 (2018)
The proline based chiral organocatalyst has been found to be an efficient catalyst for the facile synthesis of substituted 2-aryl-2H-chromenes-3-carbaldehyde. We envisioned that the iminium interaction between chiral amino catalysts and α,β-unsaturated ca
Chiral diphenylperhydroindolinol silyl ether catalyzed domino oxa-Michael-aldol condensations for the asymmetric synthesis of benzopyrans
Feng, Ya-Hui,Luo, Ren-Shi,Nie, Lin,Weng, Jiang,Lu, Gui
, p. 523 - 528 (2014/05/06)
Asymmetric domino oxa-Michael-aldol reactions between trans-cinnamaldehydes and salicylic aldehyde derivatives have been developed. Using (2S,3aS,7aS)-diphenylperhydro indolinol silyl ether 4i as the catalyst, most corresponding chiral benzopyrans can be
