An article Synthesis of chromans and kinetic resolution of 2-aryl-3-nitro-2H-chromenes via the NHC-bound azolium homoenolate pathway WOS:000489262600016 published article about ASYMMETRIC-SYNTHESIS; ENANTIOSELECTIVE SYNTHESIS; SECONDARY ALCOHOLS; MICHAEL ADDITION; ACCESS; CYCLOADDITION; REACTIVITY; CONVERSION; CHROMENES; INHIBITOR in [Bhattacharya, Aditya; Shukla, Pushpendra Mani; Kaushik, Lalit Kumar; Maji, Biswajit] Indira Gandhi Natl Tribal Univ, Dept Chem, Amarkantak 484886, Madhya Pradesh, India in 2019.0, Cited 60.0. Application In Synthesis of Methyl 3-phenylpropionate. The Name is Methyl 3-phenylpropionate. Through research, I have a further understanding and discovery of 103-25-3
Beyond the tandem oxa-Michael strategy, an N-heterocyclic carbene-catalyzed kinetic resolution approach to access highly diastereo- and enantioenriched 2-aryl-3-nitro-chromane derivatives has been developed. An efficient strategy for the kinetic resolution of racemic 2-aryl-3-nitro-2H-chromenes was also successfully achieved. This catalytic kinetic resolution method allows the synthetically valuable chiral scaffolds, chromane and 2H-chromene, to be accessed in a single catalytic and asymmetric transformation, through the NHC-bound azolium homoenolate pathway.
Application In Synthesis of Methyl 3-phenylpropionate. About Methyl 3-phenylpropionate, If you have any questions, you can contact Bhattacharya, A; Shukla, PM; Kaushik, LK; Maji, B or concate me.
Reference:
Patent; SANOFI; US2011/294788; (2011); A1;,
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