22489-94-7Relevant academic research and scientific papers
Enantioselective, desymmetrizing bromolactonization of alkynes
Wilking, Michael,Mueck-Lichtenfeld, Christian,Daniliuc, Constantin G.,Hennecke, Ulrich
, p. 8133 - 8136 (2013/07/05)
Asymmetric bromolactonizations of alkynes are possible using a desymmetrization approach. The commercially available catalyst (DHQD) 2PHAL promotes these cyclizations in combination with cheap NBS as a bromine source to give bromoenol lactones in high yield and with high enantioselectivity. The bromoenol lactone products, containing a tetrasubstituted alkene and a quaternary stereocenter, are valuable building blocks for synthetic chemistry.
