Selective syntheses of diversely substituted 2-hydroxy-4′-hydroxybenzophenones through [4 + 2] or [3 + 3] annulation of penta-3,4-dien-2-ones with 3-formylchromones-Reference-Cited by-同舟云学术

Selective syntheses of diversely substituted 2-hydroxy-4′-hydroxybenzophenones through [4 + 2] or [3 + 3] annulation of penta-3,4-dien-2-ones with 3-formylchromones

Published:2017 Issue:10 Volume:4 Page:1967-1971
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Shi Xiaonan¹²³⁴⁵,He Yan¹²³⁴⁵,Zhang Xinying¹²³⁴⁵,Fan Xuesen¹²³⁴⁵^ORCID

Affiliation:

1. School of Chemistry and Chemical Engineering

2. Collaborative Innovation Centre of Henan Province for Green Manufacturing of Fine Chemicals

3. Henan Key Laboratory of Organic Functional Molecule and Drug Innovation

4. Key Laboratory of Green Chemical Media and Reactions

5. Ministry of Education

Abstract

A selective synthesis of 2-hydroxy-4′-hydroxybenzophenones or their 3′-acylated counterparts via the cascade reactions of 3-formylchromones with diversely substituted penta-3,4-dien-2-ones is presented.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/QO/C7QO00366H

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1. Acylpyrogallols as Inhibitors of Antiapoptotic Bcl-2 Proteins

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3. Antiproliferative Prenylated Xanthones and Benzophenones from the Roots of Cudrania tricuspidata in HSC-T6 Cells