Chloramphenicol Base: A New Privileged Chiral Scaffold in Asymmetric Catalysis-Reference-Cited by-同舟云学术

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Chloramphenicol Base: A New Privileged Chiral Scaffold in Asymmetric Catalysis

Published:2019-04-03 Issue:8 Volume:11 Page:2043-2053
ISSN:1867-3880
Container-title:ChemCatChem
language:en
Short-container-title:ChemCatChem

Author:

Xiao You‐Cai¹^ORCID,Chen Fen‐Er¹²

Affiliation:

1. Sichuan Research Center for Drug Precision Industrial Technology, West China School of PharmacySichuan University Chengdu 610041 P. R. China

2. Engineering Center of Catalysis and Synthesis for Chiral Molecules, Department of ChemistryFudan University Shanghai 200433 P. R. China

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cctc.201900150

Reference63 articles.

1.

2. Asymmetric Synthesis with Chemical and Biological Methods

3. Catalytic Asymmetric Synthesis

4. Comprehensive Enantioselective Organocatalysis

5. Privileged Chiral Ligands and Catalysts

Cited by 9 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. Novel porous organic polymer supported chloramphenicol base derivatives: A highly enantioselective, recyclable heterogeneous organocatalyst for asymmetric desymmetrization reaction;Journal of Catalysis;2024-02

2. Azide‐free Enantioselective Synthesis of Clinical Antibiotic (1R,2R)‐Chloramphenicol (Chloromycetin);ChemistrySelect;2023-11-08

3. Industrial total synthesis of natural medicines;Natural Product Reports;2023

4. New conformationally flexible and recyclable aryl iodine catalysts from an inexpensive chiral source for asymmetric oxidations;Green Chemistry;2023

5. Enantioselective Synthesis of Chiral 3‐Alkynyl‐3‐Hydroxyindolin‐ 2‐Ones by Zn/bis(Sulfonamide)‐Diamine Catalyzed Asymmetric Addition of Alkynes to Isatins;Asian Journal of Organic Chemistry;2022-06

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