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Diastereoselective and Enantioselective Synthesis of Unsymmetric β,β-Diaryl-α-Amino Acid Esters via Organocatalytic 1,6-Conjugate Addition of para-Quinone Methides

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Figshare2016-06-27 更新2026-04-29 收录
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https://figshare.com/articles/dataset/Diastereoselective_and_Enantioselective_Synthesis_of_Unsymmetric_i_i_-Diaryl-_-Amino_Acid_Esters_via_Organocatalytic_1_6-Conjugate_Addition_of_i_para_i_-Quinone_Methides/3426332
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A novel strategy based on phase transfer catalysis for the diastereoselective and enantioselective direct assembly of unsymmetric β,β-diaryl-α-amino acid esters via 1,6-conjugate addition of para-quinone methides and glycine derivatives is described. This protocol also provides an alternative route to the synthetically interesting functionalized chiral tetrahydroisoquinoline and its analogues.
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2016-06-27
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