Construction of central and axial chirality via Pd(II)/Bim-catalyzed asymmetric dearomative Michael reaction of polycyclic tropones.

Autor: Zi-Li Liu, Yu-Xin Wang, Zi-Qi Yang, Yu-Heng Yang, Yin-Ping Liu, Wen-Juan Hao, Bo Jiang
Předmět:
Zdroj: Chemical Communications; 8/28/2024, Vol. 60 Issue 67, p8908-8911, 4p
Abstrakt: A highly enantioselective Pd/Bim-catalyzed dearomative Michael reaction applying polycyclic tropones as non-benzenoid aromatic Michael acceptors and arylboronic acids as aryl pronucleophiles has been developed. The bridged biaryls bearing central and axial chirality, including pentacyclic cyclohepta[b]indoles and 6,7-dihydrodibenzo- [a,c][7]annulen-5-ones, are generally generated in good to high yields and excellent enantioselectivities and can be readily transformed into useful derivatives. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index