Facileo-quinodimethane formation from benzocyclobutenes triggered by the Staudinger reaction at ambient temperature-Reference-Cited by-同舟云学术

Facileo-quinodimethane formation from benzocyclobutenes triggered by the Staudinger reaction at ambient temperature

Published:2019 Issue:44 Volume:55 Page:6205-6208
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Kohyama Aki¹²³⁴^ORCID,Koresawa Eri¹²³⁴,Tsuge Kiyoshi⁵²⁶⁴,Matsuya Yuji¹²³⁴^ORCID

Affiliation:

1. Graduate School of Medicine and Pharmaceutical Sciences

2. University of Toyama

3. Toyama 930-0194

4. Japan

5. Graduate School of Science and Engineering

6. Toyama 930-8555

Abstract

4π Ring-opening at ambient temperature triggered by the Staudinger reaction.

Funder

Japan Society for the Promotion of Science

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/2019/CC/C9CC01679A

Reference39 articles.

1. Cyclobutarenes and Related Compounds

2. Second generation of steroid synthesis via o-quinodimethane

3. Intramolecular Cycloaddition Reactions ofortho-Quinodimethanes in Organic Synthesis

4. Prediction of Thermal Isomerization Temperatures of Substituted Benzocyclobutenes to o-Quinodimethanes by Semi-Empirical Molecular Orbital Calculation

5. Stereoselective approach to potential scaffold of A-nor B-aromatic OSW-1 analogues via [4+2] cycloaddition of o-quinodimethane

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