329055-30-3Relevant academic research and scientific papers
Asymmetric Total Synthesis of (-)-α-Kainic Acid Using an Enantioselective, Metal-Promoted Ene Cyclization
Xia, Qian,Ganem, Bruce
, p. 485 - 487 (2007/10/03)
(Matrix Presented) A short and efficient asymmetric total synthesis of the title compound 1, which is an important neurotransmitter, has been achieved. The synthesis features a metal-promoted, enantioselective ene reaction that provides entry into the kainic acid ring system from very simple precursors. Moreover, the zirconium-mediated Strecker reaction, which represents an outgrowth of earlier amide-to-imine methodology developed in our laboratory, demonstrates remarkable chemoselectivity and stereoselectivity.
