详细信息
Metal-Free Intramolecular [3+2] Cycloaddition of γ-Hydroxy Acetylenic Ketones with Alkynes for the Synthesis of Naphtho[1,2- c]furan-5-ones and Its Derivatization via a Selective C(sp2)-H Deuteration Reaction ( EI收录)
文献类型:期刊文献
英文题名:Metal-Free Intramolecular [3+2] Cycloaddition of γ-Hydroxy Acetylenic Ketones with Alkynes for the Synthesis of Naphtho[1,2- c]furan-5-ones and Its Derivatization via a Selective C(sp2)-H Deuteration Reaction
作者:Ning, Si-Si[1]; Meng, Dan[1]; Zhang, Jie-Yun[1]; Liu, Shi-Lei[1]; Zhou, Ni-Ni[1]; Jin, Xiaojie[2]; Zhu, Hai-Tao[1]
第一作者:Ning, Si-Si
通信作者:Zhu, Hai-Tao
机构:[1] Shannxi Key Laboratory of Phytochemistry, College of Chemistry and Chemical Engineering, Baoji University of Arts and Sciences, Baoji, 721013, China; [2] Gansu Univ. Key Lab. for Molec. Med. and Chinese Medicine Prevention and Treatment of Major Diseases, Gansu University of Chinese Medicine, Lanzhou, 730000, China
第一机构:Shannxi Key Laboratory of Phytochemistry, College of Chemistry and Chemical Engineering, Baoji University of Arts and Sciences, Baoji, 721013, China
通信机构:[1]Shannxi Key Laboratory of Phytochemistry, College of Chemistry and Chemical Engineering, Baoji University of Arts and Sciences, Baoji, 721013, China
年份:2021
卷号:86
期号:11
起止页码:7347
外文期刊名:Journal of Organic Chemistry
收录:EI(收录号:20212610557223);Scopus(收录号:2-s2.0-85108407078)
语种:英文
外文关键词:Organic pollutants - Aromatic compounds - Regioselectivity - Deuterium
摘要:A metal-free intramolecular [3+2] cycloaddtion has been achieved by treating benzene-linked propynol-ynes with AcOH/H2O in a one-pot manner. The reaction provides greener, 100% atom-economic, highly regioselective, and more practical access to functionalized naphtho[1,2-c]furan-5-ones with valuable and versatile applications. The regioselective α-deuteration of naphtho[1,2-c]furan-5-ones has been also presented with excellent deuterium incorporation and chemical yields. Moreover, the fluorescent properties of naphtho[1,2-c]furan-5-one products have been investigated in solution. ? 2021 American Chemical Society
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