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Enantioselective Conjugate Addition of 2-Acetyl Azaarenes to β,β-Disubstituted Nitroalkene for the Construction of All-Carbon Quaternary Stereocenters.

Hongli MaLei XieZhenhua ZhangLin-Gang WuBin FuZhaohai Qin
Published in: The Journal of organic chemistry (2017)
The first highly enantioselective conjugate addition of 2-acetyl azaarenes to α-substituted-β-nitroacrylates was successfully realized under mild conditions by a Ni(II)-bisoxazoline complex, providing the desired adducts bearing an all-carbon quaternary stereocenter in high yield with excellent enantioselectivity. The products obtained in this system could be readily converted into optically active β2,2-amino esters, succinates, lactones, and lactams.
Keyphrases
  • cancer therapy
  • molecular docking
  • drug delivery
  • transition metal
  • molecular dynamics simulations