Chiral phosphoric acid catalyzed enantioselective 1,3-dipolar cycloaddition reaction of azlactones-Reference-Cited by-同舟云学术

Chiral phosphoric acid catalyzed enantioselective 1,3-dipolar cycloaddition reaction of azlactones

Published:2016 Issue:7 Volume:52 Page:1377-1380
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Zhang Zhenhua¹²³⁴⁵,Sun Wangsheng¹²³⁴⁵,Zhu Gongming¹²³⁴⁵,Yang Junxian¹²³⁴⁵,Zhang Ming¹²³⁴⁵,Hong Liang⁶⁷⁸⁹,Wang Rui¹²³⁴⁵

Affiliation:

1. Key Laboratory of Preclinical Study for New Drugs of Gansu Province

2. School of Basic Medical Sciences

3. Lanzhou University

4. Lanzhou

5. P. R. China

6. School of Pharmaceutical Sciences

7. Sun Yat-sen University

8. Guangzhou

9. China

Abstract

The first chiral phosphoric acid catalyzed highly diastereo- and enantioselective 1,3-dipolar cycloaddition reaction of azlactones and methyleneindolinones was disclosed to yield 3,3′-pyrrolidonyl spirooxindole scaffolds.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2016/CC/C5CC08989A

Reference69 articles.

1. The diverse chemistry of oxazol-5-(4H)-ones

2. Stereoselective syntheses of quaternary substituted α-amino acids using oxazol-5-(4H)-ones

3. Oxazolones in Organocatalysis, New Tricks for an Old Reagent

4. Oxazol-5-(4H)-Ones. Part 1. Synthesis and Reactivity as 1,3-dipoles

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