[3+1+1] type cyclization of ClCF2COONa for the assembly of imidazoles and tetrazoles via in situ generated isocyanides-Reference-Cited by-同舟云学术

[3+1+1] type cyclization of ClCF2COONa for the assembly of imidazoles and tetrazoles via in situ generated isocyanides

Published:2020 Issue:45 Volume:56 Page:6106-6109
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Wang Ya¹²³⁴⁵,Zhou Yao⁶⁷⁸⁵^ORCID,Song Qiuling¹²³⁴⁵^ORCID

Affiliation:

1. Institute of Next Generation Matter Transformation

2. College of Materials Science & Engineering at Huaqiao University

3. 668 Jimei Blvd, Xiamen

4. Fujian

5. P. R. China

6. College of Chemistry and Chemical Engineering

7. Hubei Normal University

8. Huangshi 435002

Abstract

A facile synthesis of imidazoles and tetrazoles via [3+1+1] type cyclization of ClCF₂COONa is developed.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Fujian Province

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/2020/CC/D0CC01919D

Reference48 articles.

1. Metal-Mediated and Metal-Catalyzed Reactions of Isocyanides

2. Isocyanoacetate Derivatives: Synthesis, Reactivity, and Application

3. Recent Developments in Isocyanide Based Multicomponent Reactions in Applied Chemistry

4. Recent advances in the synthesis of nitrogen heterocycles via radical cascade reactions using isonitriles as radical acceptors

5. A Catalytic Asymmetric Ugi-type Reaction With Acyclic Azomethine Imines

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