Asymmetric Synthesis of Chiral α‑Methyl-α,β-diamino Acid Derivatives via Group-Assisted Purification Chemistry Using N‑Phosphonyl Imines and a Ni(II)-Complexed Alanine Schiff Base
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https://figshare.com/articles/dataset/Asymmetric_Synthesis_of_Chiral_Methyl-_-diamino_Acid_Derivatives_via_Group-Assisted_Purification_Chemistry_Using_i_N_i_Phosphonyl_Imines_and_a_Ni_II_-Complexed_Alanine_Schiff_Base/3546732
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The Mannich reaction between chiral N-phosphonyl imines and a Ni(II)-complexed alanine Schiff base (Ala-Ni) is reported. With a chiral phosphonyl auxiliary, a single isomer of α-methyl-α,β-diamino acid derivative containing vicinal chiral centers, including a chiral quaternary carbon center, can be obtained simply by washing the crude mixture with cosolvents. The absolute stereochemistry of the enantiomerically pure product has been unambiguously determined by X-ray crystallographic analysis.
创建时间:
2016-08-29



