Diphenyl-Diselenide-Mediated Domino Claisen-Type Rearrangement/Cyclization of Propargylic Aryl Ethers: Synthesis of Naphthofuran-2-carboxaldehyde Derivatives-Reference-Cited by-同舟云学术

Diphenyl-Diselenide-Mediated Domino Claisen-Type Rearrangement/Cyclization of Propargylic Aryl Ethers: Synthesis of Naphthofuran-2-carboxaldehyde Derivatives

Published:2019-09-11 Issue:18 Volume:21 Page:7635-7638
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Fang Jun-Dan¹,Yan Xiao-Biao²,Lin Wu-Jie¹,Zhao Yi-Chuan¹,Liu Xue-Yuan¹^ORCID

Affiliation:

1. State Key Laboratory of Applied Organic Chemistry (SKLAOC), College of Chemistry and Chemical Engineering, Lanzhou University, 222 South Tianshui Road, Lanzhou 730000, China

2. School of Pharmacy, Anhui Medical University, 81 Meishan Road, Hefei 230032, China

Funder

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.9b02942

Reference56 articles.

1. Method of Isolation of Usnic Acid from Ramalina reticulata

2. Synthesis and Structure−Affinity−Activity Relationships of Novel Benzofuran Derivatives as MT2 Melatonin Receptor Selective Ligands