Synthesis of 1,2,4-oxadiazolidines via [3+2] cycloaddition of nitrones with carbodiimides-Reference-Cited by-同舟云学术

Synthesis of 1,2,4-oxadiazolidines via [3+2] cycloaddition of nitrones with carbodiimides

Published:2019 Issue:11 Volume:43 Page:4329-4332
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Chen Yuan¹²³⁴⁵,Fuyue Liuting¹²³⁴⁵,Wang Gangqiang¹²³⁴⁵,Wang Hang¹²³⁴⁵,Lu Chun¹²³⁴⁵,Guo Haibing¹²³⁴⁵,St. Amant Chiara⁶⁷⁸⁹,Sun Shaofa¹²³⁴⁵,Xing Yalan⁶⁷⁸⁹^ORCID

Affiliation:

1. Non-power Nuclear Technology Collaborative Innovation Center

2. School of Nuclear Technology and Chemistry & Biology

3. Hubei University of Science and Technology

4. Xianning 437100

5. China

6. Department of Chemistry

7. William Paterson University of New Jersey

8. Wayne

9. USA

Abstract

An efficient [3+2] cycloaddition of nitrones and carbodiimides has been developed.

Funder

Natural Science Foundation of Hubei Province

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2019/NJ/C9NJ00030E

Reference21 articles.

1. Application of 1,3-Dipolar Reactions between Azomethine Ylides and Alkenes to the Synthesis of Catalysts and Biologically Active Compounds

2. The Rich Chemistry Resulting from the 1,3-Dipolar Cycloaddition Reactions of Enamines and Azides

3. Current Trends towards the Synthesis of Bioactive Heterocycles and Natural Products Using 1,3-Dipolar Cycloadditions (1,3-DC) with Azomethine Ylides

4. Recent advances in the enantioselective 1,3-dipolar cycloaddition of azomethine ylides and dipolarophiles

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2. Site-Selective Deoxygenative Amination of Azine N-Oxides with Carbodiimides under Catalyst-, Activator-, Base-, and Solvent-Free Conditions;The Journal of Organic Chemistry;2021-07-14

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