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Asymmetric Synthesis of Glutamic Acid Derivatives by Silver-Catalyzed Conjugate Addition–Elimination Reactions

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NIAID Data Ecosystem2026-03-10 收录
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https://figshare.com/articles/dataset/Asymmetric_Synthesis_of_Glutamic_Acid_Derivatives_by_Silver-Catalyzed_Conjugate_Addition_Elimination_Reactions/5352763
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The enantioselective construction of a family of chiral glycine-derived aldimino esters is described. The asymmetric tandem conjugate addition–elimination procedure is characterized by its exceptional mild reaction conditions and features with an exquisite enantioselectivity profile using commercially available silver/DTBM-SegPhos catalyst, allowing for the facile preparation of a variety of substituted and chiral glutamic acid derivatives (up to 99% ee) bearing Schiff base in a straightforward manner.
创建时间:
2017-08-28
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