Y
Ying Huang
Researcher at Changsha University of Science and Technology
Publications - 7
Citations - 343
Ying Huang is an academic researcher from Changsha University of Science and Technology. The author has contributed to research in topics: Chemistry & Medicine. The author has an hindex of 4, co-authored 5 publications receiving 195 citations.
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Journal ArticleDOI
Visible-light-induced decarboxylative acylation of quinoxalin-2(1H)-ones with α-oxo carboxylic acids under metal-, strong oxidant- and external photocatalyst-free conditions
Long-Yong Xie,You-Shu Bai,Xiang-Qin Xu,Xia Peng,Hai-Shan Tang,Ying Huang,Ying-Wu Lin,Zhong Cao,Wei-Min He +8 more
TL;DR: In this paper, a mild and eco-friendly visible-light-induced decarboxylative acylation of quinoxalin-2(1H)-ones and α-oxo carboxylic acids with ambient air as the sole oxidant at room temperature was established.
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Visible-light-promoted direct C–H/S–H cross-coupling of quinoxalin-2(1H)-ones with thiols leading to 3-sulfenylated quinoxalin-2(1H)-ones in air
Long-Yong Xie,Yan-Ling Chen,Li Qin,Yuan Wen,Jian-Wei Xie,Jia-Xi Tan,Ying Huang,Zhong Cao,Wei-Min He,Wei-Min He +9 more
TL;DR: A new and efficient visible-light-mediated strategy has been developed for the synthesis of 3-sulfenylated quinoxalin-2(1H)-ones via rhodamine B catalyzed C–H/S–H cross-coupling of quinxalin-1H-ones with thiols in air at room temperature.
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Visible-light-initiated malic acid-promoted cascade coupling/cyclization of aromatic amines and KSCN to 2-aminobenzothiazoles without photocatalyst
Wei-Bao He,Lan-Qing Gao,Xin-Jie Chen,Zhi-Lin Wu,Ying Huang,Zhong Cao,Xinhua Xu,Weimin He,Weimin He +8 more
TL;DR: By using ambient air as the oxidant and malic acid as the promoter, a practical method for the preparation of 2-aminobenzothiazoles through visible-light-initiated cascade reaction of aromatic amines and KSCN in eco-friendly bis(methoxypropy)ether under metal-, hazardous additive-, photocatalyst-free conditions was established.
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1,2-Diethoxyethane catalyzed oxidative cleavage of gem-disubstituted aromatic alkenes to ketones under minimal solvent conditions
Kai-Jian Liu,Ji-Hui Deng,Tang-Yu Zeng,Xin-Jie Chen,Ying Huang,Zhong Cao,Ying-Wu Lin,Wei-Min He +7 more
TL;DR: In this article, an efficient protocol for the construction of various aryl-alkyl and diaryl ketones through oxidative cleavage of gem-disubstituted aromatic alkenes under minimal solvent conditions has been achieved.
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Copper(i)-catalyzed intermolecular cyanoarylation of alkenes: convenient access to α-alkylated arylacetonitriles.
TL;DR: A novel Cu(i)-catalyzed intermolecular cyanoarylation of alkenes with diaryliodonium salts as a radical arylating reagent and tetra-butylammonium cyanide as an electrophilic cyanating reagents was established.