Detection of enantiomers of chiral primary amines by 1H NMR analysis via enamine formation with an enantiopure γ-position aldol product of a β-keto ester-Reference-Cited by-同舟云学术

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Detection of enantiomers of chiral primary amines by 1H NMR analysis via enamine formation with an enantiopure γ-position aldol product of a β-keto ester

Published:2018-06 Issue:23 Volume:59 Page:2248-2250
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Zhang Dongxin,Chuang Po-Shun^ORCID,Cao Dong,Krishna Yarkali,Shilpa Kola,Tanaka Fujie^ORCID

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference31 articles.

1. Lewis Acid Enabled Copper-Catalyzed Asymmetric Synthesis of Chiral β-Substituted Amides

2. Catalytic Asymmetric Umpolung Allylation of Imines

3. Stereospecific Substitution of Allylic Alcohols To Give Optically Active Primary Allylic Amines: Unique Reactivity of a (P,alkene)Ir Complex Modulated by Iodide

4. Intermolecular Alkyl Radical Additions to Enantiopure N-tert-Butanesulfinyl Aldimines

5. Simple organic molecules as catalysts for enantioselective synthesis of amines and alcohols

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Direct Catalytic Asymmetric Synthesis of Oxindole-Derived δ-Hydroxy-β-ketoesters by Aldol Reactions;Organic Letters;2019-11-20

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