Mechanism and Regioselectivity of 1,3‐Dipolar Cycloaddition of Nitrile Oxides to 3‐Methylene Oxindole: A Density Functional Theory Study-Reference-Cited by-同舟云学术

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Mechanism and Regioselectivity of 1,3‐Dipolar Cycloaddition of Nitrile Oxides to 3‐Methylene Oxindole: A Density Functional Theory Study

Published:2020-07-24 Issue:28 Volume:5 Page:8421-8428
ISSN:2365-6549
Container-title:ChemistrySelect
language:en
Short-container-title:ChemistrySelect

Author:

Luo Xiaoling¹,Liu Song²,Lan Yu²³^ORCID

Affiliation:

1. Chongqing Key Laboratory of Inorganic Functional Materials, College of ChemistryChongqing Normal University Chongqing 401331 China

2. Chongqing Key Laboratory of Theoretical and Computational ChemistrySchool of Chemistry and Chemical EngineeringChongqing University Chongqing 400030 China

3. College of Chemistryand Institute of Green CatalysisZhengzhou University Zhengzhou Henan 450001 China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/slct.202002672

Reference107 articles.

2. The isoxazoline route to the molecules of nature

3. Isoxazoline containing natural products as anticancer agents: A review

4. Recent advances in the synthesis of biologically active spirooxindoles

5. Enantioselective Synthesis of Isoxazoline N-Oxides via Pd-Catalyzed Asymmetric Allylic Cycloaddition of Nitro-Containing Allylic Carbonates

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1. A computational study of 1,3-dipolar cycloadditions of nitrile oxides with dienes;Tetrahedron;2023-06

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