Extending the Synthetic Utilities of the Tandem Cyclic Sulfate Rearrangement-Opening Process: Synthesis of β-Hydroxy-γ-phenyl-γ-lactam-Reference-Cited by-同舟云学术

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Extending the Synthetic Utilities of the Tandem Cyclic Sulfate Rearrangement-Opening Process: Synthesis of β-Hydroxy-γ-phenyl-γ-lactam

Published:2016-12 Issue:12 Volume:37 Page:2091-2093
ISSN:1229-5949
Container-title:Bulletin of the Korean Chemical Society
language:en
Short-container-title:Bull. Korean Chem. Soc.

Author:

Lee Nagum¹,Yu Min Lee¹,Jun Hyeyeon¹,Ko Soo Y.¹

Affiliation:

1. Department of Chemistry; Ewha Womans University; Seoul 120-750 Korea

Publisher

Wiley

Subject

General Chemistry

Reference15 articles.

1. SNaRIs, NaSSAs, and NaRIs: new agents for the treatment of depression

2. Review of the pharmacokinetics and metabolism of reboxetine, a selective noradrenaline reuptake inhibitor

3. Carboazidation of Chiral Allylsilanes: Experimental and Theoretical Investigations

4. Nucleophilic Ring-Opening of Epoxide and Aziridine Acetates for the Stereodivergent Synthesis of β-Hydroxy and β-Amino γ-Lactams

5. The synthesis of (R,S)-reboxetine employing a tandem cyclic sulfate rearrangement—opening process

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. Synthesis of (S,S )-Reboxetine;Bulletin of the Korean Chemical Society;2018-11-25

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