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Synthesis of carbonylated heteroaromatic compounds via visible-light-driven intramolecular decarboxylative cyclization of o-alkynylated carboxylic acids
Chemical Communications ( IF 4.3 ) Pub Date : 2017-07-06 00:00:00 , DOI: 10.1039/c7cc04813k Fei Gao 1, 2, 3, 4 , Jiu-Tao Wang 1, 2, 3, 4 , Lin-Lin Liu 1, 2, 3, 4 , Na Ma 1, 2, 3, 4 , Chao Yang 1, 2, 3, 4 , Yuan Gao 4, 5, 6, 7 , Wujiong Xia 1, 2, 3, 4
Chemical Communications ( IF 4.3 ) Pub Date : 2017-07-06 00:00:00 , DOI: 10.1039/c7cc04813k Fei Gao 1, 2, 3, 4 , Jiu-Tao Wang 1, 2, 3, 4 , Lin-Lin Liu 1, 2, 3, 4 , Na Ma 1, 2, 3, 4 , Chao Yang 1, 2, 3, 4 , Yuan Gao 4, 5, 6, 7 , Wujiong Xia 1, 2, 3, 4
Affiliation
An efficient strategy for the easy access to carbonylated heteroaromatic compounds has been developed via a visible-light-promoted intramolecular decarboxylative cyclization reaction of o-alkynylated carboxylic acids. This method is characterized by its benign conditions and the tolerance to a wide range of functionalities.
中文翻译:
羰基的杂芳族化合物的合成通过的可见光驱动的分子内环化脱羧ø -alkynylated羧酸
已经通过可见光促进了邻炔基化羧酸的分子内脱羧环化反应,开发了一种易于获得羰基杂芳族化合物的有效策略。该方法的特点是其良性条件和对多种功能的耐受性。
更新日期:2017-07-28
中文翻译:
羰基的杂芳族化合物的合成通过的可见光驱动的分子内环化脱羧ø -alkynylated羧酸
已经通过可见光促进了邻炔基化羧酸的分子内脱羧环化反应,开发了一种易于获得羰基杂芳族化合物的有效策略。该方法的特点是其良性条件和对多种功能的耐受性。