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酸促进的一锅法合成取代呋喃和 6-甲基吡嗪-2(1H)-酮衍生物,通过原位形成的丙二烯中间体。

Acid-Promoted One-Pot Synthesis of Substituted Furan and 6-Methylpyrazin-2(1 H)-one Derivatives via Allene Intermediate Formed in Situ.

机构信息

Key Laboratory for Asymmetric Synthesis and Chiral Technology of Sichuan Province , Chengdu Institute of Organic Chemistry, Chinese Academy of Sciences , Chengdu , 610041 , China.

University of Chinese Academy of Sciences , Beijing 100049 , China.

出版信息

ACS Comb Sci. 2018 May 14;20(5):292-297. doi: 10.1021/acscombsci.8b00005. Epub 2018 Apr 11.

DOI:10.1021/acscombsci.8b00005
PMID:29620860
Abstract

Under the acidic conditions, substituted furans were constructed from γ-alkynyl ketones through corresponding allene intermediates in one-pot. The methodology was also tailored to a series of the Ugi reaction products for the synthesis of 6-methylpyrazin-2(1 H)-one derivatives. The current method offered significant advantages for the combinatorial applications of these chemical scaffolds.

摘要

在酸性条件下,通过相应的丙二烯中间体,γ-炔基酮一锅法构建取代呋喃。该方法也适用于一系列 Ugi 反应产物,用于合成 6-甲基吡嗪-2(1H)-酮衍生物。该方法为这些化学支架的组合应用提供了显著的优势。

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