Preparation of polysubstituted dihydrofurans through a PhI(OAc)2-promoted haloenolcyclization of olefinic dicarbonyl compounds-Reference-Cited by-同舟云学术

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Preparation of polysubstituted dihydrofurans through a PhI(OAc)2-promoted haloenolcyclization of olefinic dicarbonyl compounds

Published:2018 Issue:40 Volume:16 Page:7454-7460
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Liu Ji¹²³⁴,Liu Qing-Yun¹²³⁴,Fang Xing-Xiao¹²³⁴,Liu Gong-Qing¹²³⁴^ORCID,Ling Yong¹²³⁴^ORCID

Affiliation:

1. College of Pharmacy

2. Nantong University

3. Nantong 226001

4. People's Republic of China

Abstract

A direct synthesis of highly functionalized dihydrofurans and furans from olefinic dicarbonyl compounds is reported herein.

Funder

Government of Jiangsu Province

Nantong University

Jiangsu Province Postdoctoral Science Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/OB/C8OB02161A

Reference56 articles.

1. Acetylcholinesterase inhibitory dimeric indole derivatives from the marine actinomycetes Rubrobacter radiotolerans

2. Asymmetric synthesis of tanshindiol A.

3. A new route for the synthesis of furanoflavone and furanochalcone natural products

4. Recent applications in natural product synthesis of dihydrofuran and -pyran formation by ring-closing alkene metathesis

5. Biotransformation of 20(R)-panaxatriol by Mucor racemosus and the anti-hepatic fibrosis activity of some products

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