Ganesan, Divakar; Chennapuram, Madhu; Begum, Zubeda; Seki, Chigusa; Okuyama, Yuko; Kwon, Eunsang; Uwai, Koji; Tokiwa, Michio; Tokiwa, Suguru; Takeshita, Mitsuhiro; Nakano, Hiroto published the artcile< Sugar based γ-amino alcohol organocatalyst for asymmetric michael addition of β-keto esters with nitroolefins>, Application In Synthesis of 5153-70-8, the main research area is sugar amino alc organocatalyst Michael addition ketoester nitroolefin.
Sugar based γ-amino alc. was used in asym. Michael addition of β-keto esters with nitroolefins for the first time affording the corresponding several chiral Michael adducts bearing quaternary chiral carbon center in moderate to good chem. yields and stereoselectivities (up to 98%, up to dr. 95:5, up to 84% ee).
Heterocycles published new progress about Alkenes, nitro Role: RCT (Reactant), RACT (Reactant or Reagent). 5153-70-8 belongs to class chlorides-buliding-blocks, and the molecular formula is C8H6ClNO2, Application In Synthesis of 5153-70-8.
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics