Useful 1,2-dioxygenated dienes: syntheses and Diels–Alder reactions <i>en route</i> to substituted 2-naphthols and phenols-Reference-Cited by-同舟云学术

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Useful 1,2-dioxygenated dienes: syntheses and Diels–Alder reactions en route to substituted 2-naphthols and phenols

Published:2024 Issue: Volume: Page:
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Teng Jiabing¹,Zhang Xifang¹,Song Ying¹,Chen Nayu¹,Zhang Yuanfei¹²^ORCID

Affiliation:

1. Guangxi Key Laboratory of Natural Polymer Chemistry and Physics, Nanning Normal University, Nanning 530001, China

2. State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou 350002, China

Abstract

The alkenylation reaction of vinylene carbonate with vinyl triflates using a Pd catalyst provides an access to 1,2-dioxygenated dienes, which undergo a tandem DA cycloaddition/decarboxylative aromatization reaction to give 2-naphthols and phenols.

Funder

Natural Science Foundation of Guangxi Zhuang Autonomous Region

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/QO/D4QO01235F

Reference59 articles.

1. Catalytic Enantioselective Diels-Alder Reactions: Methods, Mechanistic Fundamentals, Pathways, and Applications

2. The Diels-Alder Reaction in Total Synthesis

3. Triazines: Syntheses and Inverse Electron-demand Diels–Alder Reactions

4. Inverse‐Electron‐Demand Diels–Alder Reactions of 2‐Pyrones: Bridged Lactones and Beyond

5. Industrial Applications of the Diels-Alder Reaction

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