DMSO-promoted direct δ-selective arylation of <i>p</i>-quinone methenylpiperidine bearinides to generate fuchsones under metal-free conditions by employing <i>p</i>-QMs themselves or substituted phenols as aryl sources-Reference-Cited by-同舟云学术

DMSO-promoted direct δ-selective arylation of p-quinone methenylpiperidine bearinides to generate fuchsones under metal-free conditions by employing p-QMs themselves or substituted phenols as aryl sources

Published:2023 Issue:35 Volume:21 Page:7151-7157
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Wang Kunpeng¹,Li Jingping¹,Zhang Haoxiang¹,Chen Yan¹,Li Mengfan¹,Xu Junju²³,Liao Benren⁴,Yi Weiyin¹^ORCID

Affiliation:

1. School of Perfume and Aroma Technology, Shanghai Institute of Technology, Shanghai 201418, P. R. China

2. College of Tabacco Science, Yunnan Agricultural University, Kunming 650201, P. R. China

3. Key Laboratory of Sustainable Utilization of Plateau characteristic spice plant resources, Education Department of Yunnan Province 650201, P. R. China

4. Shanghai No. 4 Reagent Chemical Co., Ltd, Shanghai 201512, P. R. China

Abstract

Two DMSO-promoted protocols for direct δ-selective arylation synthesis of symmetrical and unsymmetrical fuchsones from p-QMs under metal-free conditions were described.

Funder

Shanghai Institute of Technology

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/OB/D3OB01018J

Reference112 articles.

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