[3 + 2] Cycloaddition of Oxazol-5-(4H)-ones with Nitrones for Diastereoselective Synthesis of Isoxazolidin-5-ones-Reference-Cited by-同舟云学术

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[3 + 2] Cycloaddition of Oxazol-5-(4H)-ones with Nitrones for Diastereoselective Synthesis of Isoxazolidin-5-ones

Published:2016-12-20 Issue:1 Volume:19 Page:26-29
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Zhao Hong-Wu¹^ORCID,Liu Yue-Yang¹,Zhao Yu-Di¹,Pang Hai-Liang¹,Chen Xiao-Qin¹,Song Xiu-Qing¹,Tian Ting¹,Li Bo¹,Yang Zhao¹,Du Juan¹,Feng Ning-Ning¹

Affiliation:

1. College of Life Science and Bio-engineering, Beijing University of Technology, No. 100 Pingleyuan, Chaoyang District, Beijing 100124, China

Funder

Beijing Municipal Commission of Education

Natural Science Foundation of Beijing Municipality

Beijing University of Technology

Basic Research Foundation, Beijing University of Technology

Beijing Municipality

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.6b03206

Reference43 articles.

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

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

3. Reactivity of Oxazol-5-(4H)-ones and Their Application toward Natural Product Synthesis

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

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

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1. Reactions of Oxazol-5(4H)-ones Involving Organosilicone Reagents (A Review);Russian Journal of Organic Chemistry;2024-05

2. Asymmetric Inverse-Electron-Demand 1,3-Dipolar Cycloadditions Using Organocatalysts;HETEROCYCLES;2023

3. Isoxazoles;Comprehensive Heterocyclic Chemistry IV;2022

4. A Photoactivatable Formaldehyde Donor with Fluorescence Monitoring Reveals Threshold To Arrest Cell Migration;Journal of the American Chemical Society;2020-01-03

5. Organocatalytic asymmetric [4+2] cyclization of 2-benzothiazolimines with azlactones: access to chiral benzothiazolopyrimidine derivatives;Chemical Communications;2020

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