Chiral phosphoric acid catalyzed enantioselective inverse-electron-demand oxa-Diels–Alder reactions to synthesize chiral tricyclic tetrahydropyran derivatives-Reference-Cited by-同舟云学术

Chiral phosphoric acid catalyzed enantioselective inverse-electron-demand oxa-Diels–Alder reactions to synthesize chiral tricyclic tetrahydropyran derivatives

Published:2024 Issue:1 Volume:11 Page:211-216
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Tang Cong-Yun¹²,Wu Jie²³,Ji Feng-Ting¹²,Tian Fang⁴,Peng Lin¹,Wang Liang-Liang²^ORCID

Affiliation:

1. School of Food and Chemical Engineering, Shaoyang University, Shaoyang, 422000, P.R. China

2. State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, 650201, PR China

3. University of Chinese Academy of Sciences, 101408, Beijing, P.R. China

4. Key Laboratory of Asymmetric Synthesis and Chirotechnology of Sichuan Province, Chengdu Institute of Organic Chemistry, Chinese Academy of Sciences, Chengdu 610041, P. R. China

Abstract

A series of enantioenriched trans-fused octahydropyranofuran or octahydropyranopyran-containing tricyclic derivatives were accessed through chiral phosphoric acid catalyzed IEDODA reactions.

Funder

Chinese Academy of Sciences

Youth Innovation Promotion Association

Yunnan Provincial Science and Technology Department

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2024/QO/D3QO01615C

Reference26 articles.

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4. Recent Developments in Catalytic Asymmetric Inverse-Electron-Demand Diels–Alder Reaction

5. Switchable Diastereoselectivity in Enantioselective [4+2] Cycloadditions with Simple Olefins by Asymmetric Binary Acid Catalysis