1402044-01-2Relevant academic research and scientific papers
Diphenyl-Diselenide-Mediated Domino Claisen-Type Rearrangement/Cyclization of Propargylic Aryl Ethers: Synthesis of Naphthofuran-2-carboxaldehyde Derivatives
Fang, Jun-Dan,Yan, Xiao-Biao,Lin, Wu-Jie,Zhao, Yi-Chuan,Liu, Xue-Yuan
supporting information, p. 7635 - 7638 (2019/10/14)
A diphenyl-diselenide-mediated Claisen-type rearrangement/cyclization of propargylic aryl ethers under metal-free conditions is developed, affording various naphthofuran-2-carboxaldehydes in moderate to excellent yield. The broad substrate scope and excel
Microwave-assisted Claisen rearrangement of naphthyl 2-propynyl ethers: Synthesis of naphthofurans
Prasada Rao Lingam,Dahale, Dnyaneshwar H.,Mukkanti, Kagga,Gopalan, Balasubramanian,Thomas, Abraham
, p. 5695 - 5698 (2012/10/29)
An efficient two-step approach for the synthesis of naphtho[1,2-b]furans and naphtho[2,1-b]furans has been developed. Various functionalized propargyl alcohols were etherified with α- or β-naphthol under Mitsunobu reaction conditions to give naphthyl 2-pr
