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Yan-Qing Liu

Researcher at Chengdu University of Traditional Chinese Medicine

Publications -  21
Citations -  594

Yan-Qing Liu is an academic researcher from Chengdu University of Traditional Chinese Medicine. The author has contributed to research in topics: Catalysis & Organocatalysis. The author has an hindex of 9, co-authored 16 publications receiving 239 citations.

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Asymmetric organocatalysis: an enabling technology for medicinal chemistry

TL;DR: A comprehensive overview of the applications of asymmetric organocatalysis in medicinal chemistry can be found in this article, with a focus on the preparation of antiviral, anticancer, neuroprotective, cardiovascular, antibacterial, and antiparasitic agents, as well as several miscellaneous bioactive agents.
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Radical Acylfluoroalkylation of Olefins through N‐Heterocyclic Carbene Organocatalysis

TL;DR: With this protocol, over 120 examples of functionalized ketones with diverse fluorine substituents have been facilely synthesized in up to 99% yield with complete regioselectivity with preliminary results on the catalytic asymmetric variant of the olefin difunctionalization process.
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Regiodivergent construction of medium-sized heterocycles from vinylethylene carbonates and allylidenemalononitriles

TL;DR: P palladium-catalyzed, regiodivergent[5 + 4] and [5 + 2] annulations of vinylethylene carbonates and allylidenemalononitriles are reported, describing the production of over 50 examples of nine- and seven-membered heterocycles in high isolated yields and excellent regioselectivities.
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Diastereoselective Construction of 6,8-Dioxabicyclo[3.2.1]octaneFrameworks from Vinylethylene Carbonates via Palladium-Organo RelayCatalysis

TL;DR: The 6,8-dioxabicyclo[3.2.1] octane (6,8 -DOBCO) architecture widely exists in a broad spectrum of bioactive natural products, and the development of efficient and convenient protocols to construct th...
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Highly Chemo- and Diastereoselective Construction of Quaternary Stereocenters through Palladium-Catalyzed [3 + 2] Cyclization of 5-Alkenyl Thiazolones.

TL;DR: A highly chemo- and diastereoselective cyclization of vinylethylene carbonates and 5-alkenyl thiazolones through palladium catalysis and a variety of amide monothioacetals (AMTA) with two quaternary stereocenters are facilely synthesized.