Redox neutral [4+2] benzannulation of dienals and tertiary enaminones for benzaldehyde synthesis-Reference-Cited by-同舟云学术

Redox neutral [4+2] benzannulation of dienals and tertiary enaminones for benzaldehyde synthesis

Published:2018 Issue:54 Volume:54 Page:7475-7478
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Yang Lu¹²³⁴,Wei Li¹²³⁴,Wan Jie-Ping¹²³⁴^ORCID

Affiliation:

1. College of Chemistry and Chemical Engineering

2. Jiangxi Normal University

3. Nanchang 330022

4. P. R. China

Abstract

The [4+2] benzannulation reactions between tertiary enaminones and dienals have been developed for the synthesis of polyfunctionalized benzaldehydes, providing a new access to benzaldehydes alongside the classical formylation strategy.

Funder

National Natural Science Foundation of China

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/2018/CC/C8CC03514H

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