Catalytic Enantioselective Steglich-Type Rearrangement of Enol Lactones: Asymmetric Synthesis of Spirocyclic 1,3-Diketones-Reference-Cited by-同舟云学术

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Catalytic Enantioselective Steglich-Type Rearrangement of Enol Lactones: Asymmetric Synthesis of Spirocyclic 1,3-Diketones

Published:2022-11-03 Issue:22 Volume:87 Page:15031-15041
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Zhang Xiao-Yan¹,Lu Ka¹,Guo Bao-Kuan¹,Shao Ya-Ping¹,Wang Hong²^ORCID,Zhang Fu-Min¹^ORCID,Tu Yong-Qiang¹³^ORCID,Zhang Xiao-Ming¹³^ORCID

Affiliation:

1. State Key Laboratory of Applied Organic Chemistry, School of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000, P. R. China

2. School of Pharmaceutical Sciences, Zhejiang University of Technology, Hangzhou 310014, P. R. China

3. Beijing National Laboratory for Molecular Sciences, Beijing 100109, P. R. China

Funder

Ministry of Science and Technology of the People's Republic of China

Central University Basic Research Fund of China

Science and Technology Commission of Shanghai Municipality

National Natural Science Foundation of China

Higher Education Discipline Innovation Project

Beijing National Laboratory for Molecular Sciences

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.2c01421

Reference52 articles.

1. Über eine einfache darstellung von acyl-oxazolinonen-(5) aus 5-acyloxy-oxazolen II. Mitteilung über hypernucleophile acylierungskatalysatoren

2. Enantioselective Construction of Quaternary Stereocenters: Rearrangements of O-Acylated Azlactones Catalyzed by a Planar-Chiral Derivative of 4-(Pyrrolidino)pyridine

3. Development of Chiral Nucleophilic Pyridine Catalysts: Applications in Asymmetric Quaternary Carbon Synthesis

4. A Metallocene-Pyrrolidinopyridine Nucleophilic Catalyst for Asymmetric Synthesis

5. Enantioselective TADMAP-Catalyzed Carboxyl Migration Reactions for the Synthesis of Stereogenic Quaternary Carbon

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